ArticlePDF Available

PERSPECTIVES AND POSSIBILITIES OF INDIAN SPECIES OF GENUS PHYSALIS (L.) – A COMPREHENSIVE REVIEW

Authors:
www.ejpmr.com
326
Sharma et al. European Journal of Pharmaceutical and Medical Research
PERSPECTIVES AND POSSIBILITIES OF INDIAN SPECIES OF
GENUS PHYSALIS (L.) A COMPREHENSIVE REVIEW
Navdeep Sharma, Anisha Bano, Harcharan S. Dhaliwal, Vivek Sharma*
Akal School of Biotechnology, Eternal University, Baru Sahib-173101 (H.P.) India.
Article Received on 13/01/2015 Article Revised on 04/02/2015 Article Accepted on 25/02/2015
ABSTRACT
Present review article reveals the importance of different species of
genus Physalis (L.) distributed in India and this extensive research
information on different species is significant for future researchers
worldwide. In this article cytomorphological, phytochemical,
biological activities and ethnobotanical inputs have been extensively
recorded for different species of the genus Physalis (L.). As a part of
our investigation on cytomorphological and phytochemical aspects for important medicinal
plants from India, the aim of this review article is to provide precise, truthful and detailed
information of six Indian species of the genus Physalis (L.) viz., (P. alkekengi L.; P. angulata
L.; P. ixocarpa Brot. Ex. DC.; P. longifolia Nutt.; P. minima L.; P. peruviana L.). As per our
knowledge, there is not even a single, combined, constructive review report available about
the different Indian species of genus Physalis (L.) evaluated by using cytomorphological,
ethnobotanical, phytochemical and biological activities based aspects from India.
KEYWORDS: Physalis spp., Cytomorphology, Phytochemistry, Ethnobotany, Biological
Activities.
INTRODUCTION
Plants and herbs are used in preparation of medicines and treatment of various diseases from
the ancient time. Over the past two decades there is increase in the use of herbal medicine.
According to the World Health Organization, 70-80% of world population uses the plant
derived traditional methods for the treatment of various health problems.[1, 2] The availability
of medicines plants and their cheaper cost in comparison to modern therapeutic agents makes
them more attractive as therapeutic agents.[3] India is crowned with a rich wealth of medicinal
plants, which ranked India on the top of the list for the production of herbal medicines.[4] It is
Review Article
ISSN 3294-3211
EJPMR
EUROPEAN JOURNAL OF PHARMACEUTICAL
AND MEDICAL RESEARCH
www.ejpmr.com
ejpmr, 2015,2(2), 326-353
*Correspondence for
Author
Dr. Vivek Sharma
Akal School of
Biotechnology, Eternal
University, Baru Sahib-
173101 (H.P.) India
www.ejpmr.com
327
Sharma et al. European Journal of Pharmaceutical and Medical Research
clear that, the medicinal value of these herbs and plants is due to the bioactive constituents
present in the plants that have physiological effects on the human body. With the help of
various phytochemical techniques, it is easy to isolate and introduce valuable drugs in
modern medicinal system.[5] The present study is therefore, a continuation of on-going
labours to explore the traditional knowledge, cultural practices, cytomorphological, biological
and biochemical importance in these study areas with the ultimate aim of evaluating
medicinal plants for diversity and utilization pattern and also to protect from disappearance of
this treasure. Therefore, due to importance of different species of the genus Physalis L., it has
been taken in to consideration for future exploration and evaluation. As per the literature,
genus Physalis L. comprises 120 species distributed all over world and out of which six
species are distributed in different geographic regions of India. As a part of our investigation
on cytomorphological, phytochemical, biological activities and ethnobotanical inputs for
important medicinal plants from India, the aim of this review article is to provide precise,
truthful and detailed information of six Indian species of the genus Physalis L. (P. alkekengi
L.; P. angulata L.; P. ixocarpa Brot. Ex. DC.; P. longifolia Nutt.; P. minima L.; P. peruviana
L.) to future researchers worldwide. As per our knowledge, there is not even a single,
combined, constructive review report available about the different Indian species of genus
Physalis L. evaluated by using cytomorphological, ethnobotanical, phytochemical and
biological activities based aspects from India.
Botanical Classification Vernacular Name
Kingdom: Plantae Ben.: Ban tipariya
Order: Solanales Guj.: Parpoti, Popti, Moti popti
Family: Solanaceae Hin.: Rassbhary, Thlati pati, Tipari
Subfamily: Solanoideae Kan.: Gudde hannu
Tribe: Physaleae Mal.: Njodi njotta
Subtribe: Physalinae Mar.: Chirboti, Dhan mori
Genus: Physalis (L.) Ori.: Phutka
Tam.: Tholtakkali
Tel.: Kupanti, Budda budama, Budda basara
www.ejpmr.com
328
Sharma et al. European Journal of Pharmaceutical and Medical Research
Trade and Common Name: Winter cherry, Cape goose berry, Hogweed, Balloon cherry,
Coqueret, Strawberry tomato, Cutleaf ground cherry, Wild tomato, Winter tomato, Winter
cherry, Cow pops, Chinese lantern, Mullaca, Koropo, Camapu.
Geographic Distribution and Habitat: There are about 120 species of genus Physalis (L.)
distributed worldwide, P. alkekengi has an unknown center of origin and it is old world
species originated from Asia. Other species viz. P. angulata, P. peruviana and P. minima are
originated from tropical America.[6] P. peruviana (L.) found most commonly in Brazil. There
are six species of Physalis (L.) present in India, viz: P. alkekengi (L.); P. angulata (L.); P.
ixocarpa Brot. Ex. DC.; P. longifolia Nutt.; P. peruviana (L.) as cultivated species and P.
minima (L.) as common weed.[7] The number of species of Physalis (L.) occurring in the
India does not have the proper distinctions and certainty, this is due to introduction as weeds
and cultivated species and the hybridization problems amongst some of these species, a
reality outside their native habitats and beyond the experience of those who bred them under
captivity. Thus the various species of genus Physalis and their hybrids are now well
established weeds of disturbed landscapes and crops throughout the tropics, including Asia.[8]
Cytological Status: Cytological variations among the medicinal plants species caused by
environmental stress, genetic recombination and mutation. With the extensive study of
meiotic behavior among the populations of medicinal plants species, new cytotypes can be
recorded to look for genetic diversity. The genus Physalis (L.) is extensively studied by
various researchers from India and abroad. Here in this article the cytological data of six
Indian species have been extensively compiled and discussed. The cytological analysis of
first Indian species viz., P. alkekengi (L.) was done by various researchers world-wide and
reported 2n=2x=24.[9-11] The other variety named P. alkekengi var. franchetii (Mast.) Makino
was also analysed cytologically and reported 2n=2x= 24.[12] The second Indian species P.
angulata (L.) was cytologically well studied and reported 2n=4x=48.[13-17] The third species
of genus Physalis L. i.e. P. longifolia reported to have chromosome count 2n=4x=48 [18],
whereas 2n=2x=24 was also reported for P. longifolia var. longifolia.[19] The fourth Indian
species P. minima (L.) was also extensively studied on the basis of cytology and reported to
have 2n=4x=48 and 2n=6x=72 chromosome numbers.[20-23] The fifth Indian species P.
peruviana (L.) was also well studied and reported tetraploid and hexaploid i.e. 2n=4x=48 and
2n=6x=72.[24, 25] The sixth Indian species i.e. P. ixocarpa Brot. Ex. Hornem. was
cytologically examined and showed diploid (2n=2x=24) chromosome numbers.[26-28] From
www.ejpmr.com
329
Sharma et al. European Journal of Pharmaceutical and Medical Research
the cytological data it is clear that the Indian species of the genus Physalis (L.) exhibit
different (2x, 4x and 6x) ploidy levels. The role of cytological study is to conserve the genetic
diversity of medicinal plants especially the germplasm of new cytotypes for future research
purposes.
Morphological Description: With the help of morphometric characters new morphotypes
can be recorded. The morphological aspects of all the six Indian species of the genus Physalis
have been compiled. P. angulata is an annual, erect and branching herb having much
branched stems growing to 1m height. Leaves of plant are approximately 9cm long, ovate to
elliptic, having 1-2 nodes with pointed tips. Flower of plant is up to 6mm long and pale
yellow or white in color, solitary in the leaf axis, produces small, orange edible berries
surrounded by an inflated balloon like and ovoid calyx to about 3-5mm long. Seed is 1.0 to
1.5 mm having shape of disc with pale yellow color.[29, 30] The second Indian species P.
alkekengi is also called as winter cherry and it is an herbaceous perennial, erect and
ascending herb of height 25 inch approximately. Leaves are green and 3 inch long in size,
ovate and elliptic. Flowers are whitish and solitary. Fruit is opposite, globular, berry,
tasteless, scarelet when ripe. Seeds are numerous and reniform. P. peruviana is a herbaceous,
erect, subtropical zone plant and can grow up to 0.6-0.9m, but in some cases it can grow up to
the height of 1.8m. Leaves are ovate. Flowers with five large purple spots near the base and
pollinated by the insects, wind and by auto-pollination. The fruit is globose berry, ovoid in
shape, juicy having diameter 1.25 to 2.50cm, fruit is protected by inflated calyx or fruit
basket, protects the plant from insects, birds, diseases and harsh climatic conditions.[31, 32] P.
longifolia is a small herbaceous perennial herb growing 20 to 70cm tall with somewhat oval-
shaped leaf blades 5 to 9cm long. Flowers occur in the leaf axis. The bell-shaped corolla is up
to 2 cm wide and is yellow with purplish markings around the center.[33] P. minima herb is
commonly called bladder cherry. [34] It is an annual herb, 0.5-1.5m in height having dark
green dorsal and light green ventral, ovate leaves 9.7cm long and 8.1cm broad. The flowers
are solitary and yellow. The fruit is a yellow color berry, enclosed in the calyx, which is
4.1cm long and 2.5cm broad mature in autumn.[35-40] P. ixocarpa plant is an annual branched
herb having weedy appearance. It gets 3-6 feet (0.9-1.8 m) tall and falls over and sprawls on
the ground if not given support. The flowers are yellow with purple markings. The fruit
develops inside a green and purple bladder-like calyx that looks like a small Chinese lantern
hanging from the stem.
www.ejpmr.com
330
Sharma et al. European Journal of Pharmaceutical and Medical Research
Chemical Constituents: Physalis (L.) species contains various carbohydrates, lipids,
minerals, vitamins and phytosteroles. They contribute in the withanolide type structures.
Withanolides are defined as a group of C28 ergostane type steroids with a C-22, 26 δ-lactone
group, first isolated from genus Withania (L.)[41] P. alkekengi (L.) sepals contain zeaxanthin
and betacryptoxanthin esters or carotenoid esters useful as food additives or nutraceuticals.[42]
The four steroids, physalin Y, physalin Z, physalin I and physalin II are isolated from the
calyces of P. alkekengi.[43] P. minima (L.) contains phenols, alkaloids, steroids, saponins,
fatty acids and flavonoids.[44, 45] The seeds of P. minima contain oil (palmitic, stearic, oleic,
linoleic and small amounts of hexadecenoic and hydroxy fatty acid) and protein.[46] The
leaves, roots stem of the plant contain withanone, withaferin A, withanolide A, stigmasterol
and sitosterol, while fruits and flowers contain withanolide A, withanone, withaferin,
dihydroxyphysalin B 2-4, physalin A, B and X. The plant also contain physalindicanols,
physalinicanol A, withametelins, physalin, withanolide, withanogulutins, vitasteroids,
phygrine, withaphysalin A, B, C, D, E and physalin A, C, B, D, I, L, withanone, withaferin A
and withanolide A.[47-53] There are presence of seven withanolides like physalindicanoles A
and B, withamin and withphysalin E and other includes physalin B, D, C and 3-O-glucosides
of kaempferol and quercetin. Physalin A, B, C and flavonoids, physalin H, isophysalin B and
5β, 6β-epoxyphysalin B, two new physalins have been isolated from the P. minima whole
plant.[54-56] Physalins are the main steroidal constituents and are characterized by their
modified ergostane type framework, being 16, 24-cyclo-13, 14- secosteroids.[57-66] It has also
been reported to contain withaminimin, phygrine (alkaloid), physalin L, a 13, 14-seco-16, 24
cyclosteroid, other compounds are physalin B, epoxyphysalin B, physalin D and
flavonoids.[67-73] The fruit of P. peruviana contains polyunsaturated fatty acids,
carbohydrates, vitamins A, B, C, E, K1, phytosteroles, essential minerals (phosphorus, iron,
potassium and zinc) and withanolides.[74-78] P. peruviana contain the pseudo-steroids,
physalins with physalin A, B, D, F and glycosides which show the anticancer activity.[79]
From the aerial parts of P. peruviana various withanolide glycosides such as, perulactone,
perulactone B, blumenol A, and (P)-(S)-dehydrovomifoliol have been isolated. Withanolides
E and - hydroxywithanolide E have been tested as anti-cancer agents.[80] From the whole
plant material there is isolation of two withanolides, and characterized as (20R,22R)-
5α,6β,14α,20,27-pentahydroxy-1-oxowith-24-enolide and (20S,22R)-5β,6β-epoxy-
4β,14β,15α-trihydroxy-1-oxowith-2,24-dienolide.[81] The phytochemical study of P.
longifolia leads to the isolation of three different withanolides such as, withalongolide A,
withaferin A, withalongolide B in conjugation with 22 other withanolides. These three
www.ejpmr.com
331
Sharma et al. European Journal of Pharmaceutical and Medical Research
withanolides showed the promising anti-proliferative activity against human head and neck
squamous carcinoma (JMAR and MDA, 1986) and malenoma (B16F10 and SKMEL-28) cell
lines.[82-84] P. angulata (L.) contains carbohydrates, lipids, minerals, vitamins and
phytosteroles. It also have physalins B, E, F, G, H, I and withangulatin A. Withaferin A and
withangulatin A are structurally related to each other. Flavonal glycoside named as myricetin
3-O-neohesperidoside also present.[85-87] Physalin B and F are responsible for the reduction of
Leishmania infected macrophages and intracellular parasite number in-vitro at concentrations
non-cytotoxic to macrophages.[88] P. ixocarpa has slightly acidic flavor and a very good
source of vitamins A and C. The chemical present in P. ixocarpa is ixocarpalactone A and
may have chemoprotective activities.[89]
Pharmacological and Bioactivities of Six Indian Species of Genus Physalis (L.): The
genus Physalis has great economic importance not only as food supplier, but for its important
chemical compounds. Two major groups of chemical compounds are responsible for the
various medicinal properties, the tropane alkaloids (mainly tropine and tigoidine) and the
physalins (steroid compounds). Tropanes are responsible for an anti-muscarinic activity, they
block the activity of neurotransmitter acetylcholine by binding to muscarinic receptors of the
parasympathetic nervous system. These chemical compounds are useful in treatment of
gastrointestinal and muscular spasms and Perkinsons disease.[90, 91] Physalins are under
attention because of the anti-tumour and cytotoxic activity.[92-94] Physalis has a broad
spectrum of biological activities such as antibacterial, antiseptic, abortifacient, molluscicidal,
antiprotozoal, anticancer, cytotoxic and immune modulatory activities.[95-100] But,
unfortunately these medicinal properties are not used commercially.
The six species of Physalis in India are used for their various medicinal properties viz., P.
alkekengi (L.) has various activities like, diuretic, used in urinary and skin diseases, can use
to cure worm infections and has abortifacient properties. It is also used in kidney and bladder
stone, febrile disease, inflammation, constipation, general edema, arthritis and rheumatism.
The chemical components present in the extract are physalins, citric acid and vitamin C. P.
alkekengi has the antineoplastic and cancer static activity, whereas the P. ixocarpa fruits are
very rich in vitamin C and has antiseptic properties.[101-105] P. minima is used as a tonic for
purgative and diuretic properties and extract shows antifertility and antitumor properties.[106]
It is also used in the treatment of colic, gastrophy, earache, gonorrhea and the root paste is
used for backache and odeama treatment.[107-109] The leaf juice of P. peruviana is used for
www.ejpmr.com
332
Sharma et al. European Journal of Pharmaceutical and Medical Research
worm infection treatment and bowel complaints and the plant has diuretic properties (103). P.
longifolia Nutt and other Physalis species are used as food and medicines to treat headache,
stomach trouble and to dress wounds.[110, 111] P. peruviana is a plant with different medicinal
uses, the fruit juice of P. peruviana is directly used in eye for the treatment of pterygium,
which is the common eye disease and it can cause progressive reduction of visual acuity in its
more advanced stages and may lead to blindness in Colombia.[112, 113] P. peruviana has the
anti-diabetic activity (114). Finally, P. angulata is medicinal plant used in traditional
medicine as anti-diuretic and cures the stomach troubles, analgesic, anti-rheumatic. It is also
considered as anti-pyretic, anti-nociceptive, anti-inflammatory for hepatitis and
cervicitis.[115, 116] Few most important and well defined biological activities of the six Indian
species of genus Physalis (L.) are extensively compiled and discussed.
Hepato-renoprotective Activity: Liver is the largest organ of the body and is the main site
for the various processes like carbohydrate, protein and fat metabolism, detoxification,
storage of bile and storage of vitamins.[117] P. angulata and P. peruviana are the herbs which
are widely used in traditional medicine. Ahmed worked on the renoprotective effect of the P.
peruviana (L.) extract on acute renal injury in rats. P. peruviana extract pretreatment
improved kidney histology and reduce the level of thiobarbituric acid reactive substances and
enhanced other antioxidant enzymes in kidney homogenate compared to cisplatin group.[118]
In another study the hepatoprotective activity of P. minima was checked against paracetamol
induced hepatic injury in rats.[119] Other activities like antioxidant, antibacterial were also
tested against the ethanolic extract. The results from this study indicated that the leaves of P.
minima were possessing hepatoprotective activity in comparison with standard
hepatoprotective drug silymarin. P. peruviana roots hepato-renal protective effects were seen
against fibrosis in rats. The results were confirmed by liver and kidney histopathological
analysis. P. peruviana succeeded in protecting the liver and kidney against fibrosis.[120] P.
peruviana was evaluated for its antihepatotoxic, phytochemical analysis and the acute
toxicity of the most promising extract in rats. Water, ethanol and hexane extracts of P.
peruviana showed antihepatotoxic activities against CCl4 induced hepatotoxicity. The ethanol
and hexane extracts showed moderate activity as compared to water extract. The results were
analyzed by the serum marker enzymes. Histopathological changes caused by CCl4 were also
significantly reduced by the extract. The extract administration to rats resulted in an increase
in hepatic glutathione and decrease in malondialdehyde. Preliminary phytochemical analysis
showed the presence of various components in the crude aqueous extract. There was no acute
www.ejpmr.com
333
Sharma et al. European Journal of Pharmaceutical and Medical Research
toxicity in rats.[121] In another study, the aqueous and ethanol extracts prepared from the
whole plant were evaluated for the anti-hepatoma activity. Three human hepatoma cells, viz.
Hep G2, Hep 3B and PLC/PRF/5 were tested using XTT assay.[122]
Anti-inflammatory, Anti-arthritic and Immunomodulatory Activity: Anti-inflammatory
and anti-arthritic activities of aqueous, ethanolic and methanolic extracts of P. angulata (L.)
leaves were checked by various workers. They checked the anti-inflammatory activity by
HRBC membrane stabilization method and in-vitro anti-arthritic activity by protein
denaturation method in different concentrations and found positive response shown by the all
extracts.[123] In one of the research work of P. angulata (L.), lyophilized aqueous extract from
the roots was used to control the inflammatory response induced by the injection of 1%
carrageenan into subcutaneous rat's air pouches. The inflammatory mediators action was
evaluated by Adenosine deaminase (ADA) activity, nitrite level and prostaglandin E (2) level.
Tumor growth factor-beta level was used as a bio indicator of immunomodulatory response.
These results indicate that aqueous extracts showed powerful anti-inflammatory and
immunomodulatory activities. Juan and co-workers, worked on the fruit juice of P. peruviana
for treatment of pterygium. In this study the anti-inflammatory and cytosolic activities of the
fruit juice in rabbit eye was investigated.[124] Anti-inflammatory activity of extracts and
fractions obtained from P. peruviana calyces were analyzed in mice model of acute
inflammation.[125] The calyces were extracted using percolation, using different solvents. The
anti-inflammatory activity from P. peruviana calyces were confirmed and validated its use in
folk medicine. Fractions responsible for the anti-inflammatory action were identified and
seem promising for phyto-medicinal development. In few experiments, immunomodulatory
activities of physalins were tested from P. angulata extracts.[126] In these experiments,
Physalins B, F or G caused a reduction in nitric oxide production by macrophages stimulated
with lipopolysaccharide and interferon-g. Physalin B-treated mice had lower levels of serum
TNF-α than control mice after lipopolysaccharide challenge. When mice injected with
physalins B, F or G survived after a lethal lipopolysaccharide challenge. These results
demonstrate that seco-steroids are potent immunomodulatory substances and act through a
mechanism distinct from that of dexamethasone. On the basis of Draize test the anti-
inflammatory activity and by measuring and comparing growth rates of cultured fibroblasts
exposed and not exposed against various fruit juice concentrations were evaluated. The
results showed that the P. peruviana fruit was mild anti-inflammatory when compared with
anti-inflammatory drug methylprednisolone and a dose dependent cytotoxic effect on
www.ejpmr.com
334
Sharma et al. European Journal of Pharmaceutical and Medical Research
cultured fibroblasts was also formed. The different P. angulata (L.) extracts fractions (PA-
VII, PA-VII-A, PA-VII-B and PA-VII-C) were investigated for immunomodulatory
activity.[127] The results obtained were, PA-VII and PA-VII-C strongly enhance blastogenesis
response, PA-VII-B had moderate activity and PA-VII-A exerted only slight effect on cell
proliferation. PA-VII and PA-VII-C possessed stimulatory activity on B cells and have very
little effect on T cells. The antibody responses were also showed by PA-VII, PA-VII-B and
PA-VII-C, but not by PA-VII-A.
Aminociceptive Activity: Bastos and co-workers, identified the aminociceptive activity of
the P. angulata aqueous extract from the roots. Aqueous extract is given by half or an hour
before the acetic acid treatment which causes the abdominal contractions. Aqueous extract
inhibit these contractions. Mice treatment with extract or with morphine produced a
significant increase of the reaction time in the hot plate test. The results showed the aqueous
extract produce marked aminociceptive against the acetic acid induced visceral pain and
inflammatory pain responses induced by formalin in mice.[95]
Anti-diabetic Activity and Acute Toxicity: Sateesh and co-workers, reported the in-vitro
anti-diabetic activity on the P. angulata fruit. The extracts were prepared from powdered
material by sequential maceration method by using solvents namely, n-hexane, chloroform,
ethyl acetate, acetone and methanol. The antidiabetic activity was evaluated using inhibition
of alpha amylase and alpha glucosidase enzymes. The study reveals that the methanol
extracts of fruits inhibited both of the enzymes in-vitro.[128] From one of the research work it
has been concluded that the aqueous decoction prepared from the dry powder of P. peruviana
reduces the concentration of glucose in the guinea pigs. So, it has been concluded that the
plant have hypoglycemic activity in animal model, but at high doses plant may cause severe
intoxication.[129] The hypoglycemic effects of different extracts from the P. minima in
alloxan-induced diabetic albino rats were studied .[130] The plant parts were powdered and
extracted using boiling water using soxhlet extractor. There was mild reduction in the fasting
blood glucose level when seen with the aqueous extracts of roots and stem of P. minima. On
chronic administration the effect of P. minima leaf and flower causes a significant fall in
fasting blood sugar of rats. This concludes that the anti-diabetic efficiency leaf and flower
extract of plant is almost same and both have a potent anti-diabetic activity than all other root
and stem extracts. Abo and Lawal, evaluated the anti-diabetic activity of P. angulata
aqueous, methanolic extracts and column fraction from whole plant. The extract shows
www.ejpmr.com
335
Sharma et al. European Journal of Pharmaceutical and Medical Research
positive significant lowered blood glucose level in the alloxan diabetic rats. The fraction
shows the significant reduction of blood glucose level when compared to crude extracts.[131]
Antidiabetic potential of ethanolic roots extract of P. angulata using alloxan induced diabetes
mellitus in rats were also evaluated. The extract was prepared and analyzed their fasting
blood glucose and lipid profile. This shows the significant results by reducing the blood
glucose, cholesterol, triglycerides and low density lipoproteins, while increases the high
density lipoproteins.[132] In one of the study it is reported that, P. alkekengi has the potential
to reduce the serum glucose level in the alloxan-induced diabetic rats, administrated orally.
These results in the reduction of glucose level and activity might be due to chemical
compounds specially physalins, citric acid and vitamin C.[114]
Anti-cancerous Activity: Anti-cancer activity of P. peruviana was demonstrated by Ngern
and co-workers. The methanolic extract of the aerial parts of the whole plant of P. peruviana
showed inhibition of both the tumor necrosis factor-α (TNF-α)-induced NF-kappa B activity
and aberrantly-active Stat3 in human tumor cells. There was isolation of four new compounds
in the methanolic extracts of P. peruviana. These new isolated compounds showed the
inhibition of TNF-α-induced NF-kappa B activation.[133] It is concluded in one of the research
work, that physalin-F induces cell apoptosis in human renal carcinoma cells by targeting NF-
kappa B cells and generating oxygen species in P. angulata. It has been resulted that
physalin-F appears to be a very promising anti-cancer agent and useful for further clinical
development. [134] One pure compound 4β-Hydroxywithanolide (4βHWE) was isolated from
the plant P. peruviana and checked its anti-proliferative effect on human lung cancer cell line
(H1299) using survival, cell cycle and apoptosis analyses. DNA damage due to drug is
analyses by the alkaline comet nuclear extract assay. The results were analyzed and found
that DNA damage induced significantly in a dose dependent manner. The proliferation of
cells was inhibited by 4βHWE in both dose and time dependent manner. Half maximal
inhibitory concentrations of 4βHWE in HI299 cells, suggests that it could be a potential
therapeutic agent against lung cancer.[135]
Anti-microbial Activity: Nathiya and Dorcus worked on the antimicrobial activity of P.
minima using different bacterial strains viz., Bacillus cereus, Bacillus subtilis, Citrobacter
sp., Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae, Pseudomonas
aeruginosa, P. fluorescens and Staphylococcus aureus using agar well diffusion method. The
result revealed that the ethanolic extract of leaf and stem was found to be more effective
www.ejpmr.com
336
Sharma et al. European Journal of Pharmaceutical and Medical Research
against bacterial strains.[136] Donker et al. compared the antimicrobial activity of zinc oxide
ointment and P. angulata crude fruit extracts against Pseudomonas aeruginosa and
Staphylococcus aureus. The unformulated crude extract of plant fruit exhibited the highest
inhibitory activity against S. aureus. These result showed that plant fruit extract is useful
against the S. aureus infections.[137] The antifungal activity of P. alkekengi (L.) extracts
against Microsporum canis, Candida albicans, Trichophyton mentagrophytes and Nocardia
asteroids were evaluated. The aqueous, ethanol and methanol extracts were used against the
fungal strains using agar tube dilution method. Ethanol extracts showed the strongest
inhibition effect with minimum inhibition concentration of 15.62mg/mL for all tested fungus.
Nocardia asteroids was the most sensitive fungi found in this experimental study.[138] In other
report, the antimicrobial activity of P. angulata using essential oils from aerial and root parts
on Bacillus subtilis, Pseudomonas aeruginosa, Klebsiella pneumonia and Staphylococcus
aureus were tested. The fungal species used in this experiment were Candida torulopsis,
Candida albicans and Candida stellatoidea. The results showed the minimum inhibitory
concentrations ranging between 3.75mg/mL and 4.0mg/mL for Bacillus subtilis, Klebsiella
pneumoniae by the aerial and root extracts. The fungal strains were susceptible to the
essential oils from the aerial and root part of the plant. This study justified the use of plant for
treatment of cuts, sores, and some skin diseases often reported in folkloric medicine. Leaf and
callus extracts prepared in chloroform were found to be more effective against the pathogenic
bacteria and fungi.[139] Anti-microbial activity of methanolic extract from the aerial parts and
dichloromethane extract from the calyces of P. alkekengi was checked. These extracts were
tested against five gram-positive and five gram-negative bacteria and five Candida species.
The extracts were fractionated to isolate physalins using chromatographic techniques, and
physalin D was isolated from the extracts. The methods used to check the activity were disk
diffusion and broth micro dilution methods. The methanol extract showed moderate activity
against fungi at MICs ranging from 128 to 512 μg/mL, the dichloromethane extract and
physalin D had low activity against fungi at MICs ranging from 256 to 512 μg/mL.[140] Anti-
microbial activity of Physalis minima leaf and callus extract using solvents absolute alcohol,
benzene, chloroform, methanol and petroleum ether against pathogenic bacteria and fungi,
following broth dilution assay was evaluated.[141]
Anti-leshmaniasis Activity: The anti-leishmaniasis activity of physalins purified from P.
angulate was evaluated. This activity of physalins B, D and F was tested against intracellular
amstigotes of Leishmania amazonensis (MHOM/BR88/BA-125) and Leishmania major
www.ejpmr.com
337
Sharma et al. European Journal of Pharmaceutical and Medical Research
(MHOM/RI/-/WR-173). The in-vivo study was done in the BALB/c mice infected with
Leishmania amazonensis subcutaneously. The results showed that the physalin-F is
significantly potent against the leishmania, and suggests these chemical compounds for the
development of new therapeutic drugs for cutaneous leishmaniasis. The leishmanicidal
activity of P. minima was also analyzed by isolating two compounds and these isolated
compounds were physalins. The results showed the potent leishmanicidal against the
promastigoes of Leishmania major.[142] P. minima shows the anti-leshmaniasis, had been
investigated by isolating the different compounds. Three new physalins 1-3 and a new
withanolide 7 were isolated. The results showed that the compounds 1-6 were significant in
vitro leishmanicidal activities against promastigotes of Leishmania major.[143]
Anti-asthmatic Activity: The anti-asthmatic activity of the P. angulata roots alcoholic
extracts in albino mice was also checked, the asthma was introduced in the rats with
ovalbumin. The extract results inhibited ovalbumin induced asthma by decreasing the release
of inflammatory mediators. The anti-asthmatic activity is due to the reduction in
inflammatory mediator release.[144]
Analgesic and Anti-spasmodic Activity: The analgesic activity of methanolic extract of P.
alkekengi, using acetic acid and tail immersion method in rats was also evaluated, the
abdominal writhings were reduced when methanolic extract of the plant is given and
compared with control and standard drug Aspirin, from this it has been concluded that the
methanolic extract of P. alkekengi have significant analgesic activity.[145] Mohammad et al.,
studied the effect of hydrochloric extract of P. alkekengi ripe fruits on the uterine contraction.
The ripened fruit extract prepared by marceration method (70%). The uterus from adult non-
pregnant rat was removed and treated by KCl (60mM) or oxytocin (10mU/mL), lead to
contraction. The uterus was kept in the organ bath containing De Jalon solution and effect of
fruit extract was studied. According to the results KCl and oxytocin induced uterine
contractions were inhibited by the extract in the concentration dependent manner. The
working mechanism of this extract was mainly via calcium influx blockade, partially through
blocking β-adrenoceptors and nitric oxide synthesis.[146]
Molluscicidal Activity: The mulluscicidal activity of P. angulata (L.) was studied on
different extracts, fractions and also on the physalin modified steroids of this plant species.
The results indicated that ethyl acetate and acetone extracts from the whole plant, the
www.ejpmr.com
338
Sharma et al. European Journal of Pharmaceutical and Medical Research
ethanolic extracts of roots, the physalins extracted from stem and leaves were active against
Biomphalaria tenagophila.[147]
Gastric Inflammation and Gastric Ulcer: The effect of methanolic extract of P. minima
(L.) in gastric inflammation and gastric ulcers in rats was also investigated and when
compared to the aspirin, the methanolic extract has the lower gastric ulcer formation side
effects.[148]
Diuretic Activity: The methanolic extract of the plant P. minima was prepared by soxhlet
extractor and its diuretic effect was checked on albino wister rats. Furosemide was used as
positive control. The diuretic activity was analyzed by checking the urine volume, sodium
and potassium content. The study concluded the methanolic extracts produce a significant
diuretic activity.[149] The diuretic activity of methanolic extract of P. angulata L. were
investigated in rats, furosemide was used as the positive control. The diuretic effect of the
extract was evaluated by measuring urine volume and excretion of sodium, potassium and
chloride ion content. From the results it had been concluded that P. angulata shows the
significant diuretic activity.[150]
Anti-malarial Activity: Anti-plasmodial and cytotoxic activity of methanolic and
dichloromethane extracts of P. angulata in-vivo and in-vitro against the Plasmodium berghei
infected mice were checked by various researchers. The extract showed the significant anti-
plasmodial and anti-malarial activity.[151]
Anti-oxidant and Cytotoxic Activities: The anti-oxidant and cytotoxic activities of P.
peruviana fruit extracts were evaluated by using DPPH and MTT assay. Anti-oxidant
potential of crude extract and IC50 values were calculated as 0.43±0.003mg/mL and the IC50
values of cytotoxicity for cell lines namely HT-29, Hep3B, SaOS-2 and SH-SY5Y were
calculated as 40.79, 24.92, 15.44 and 44.24µg/mL. The plant extract had no cytotoxic effect
on MCF-7, LNCap and vero cells. According to these results P. peruviana fruit‟s crude
extract was more cytotoxic than the whole plant extract.[152] In one of the research
investigation, the antioxidant properties of leaves, stem, fruit and root of P. angulata using
methanol as a solvent for extracts was also evaluated. The DPPH, superoxide, nitric oxide,
hydrogen peroxide and hydroxyl radical were used for the investigation. The fruit and leaf
extracts were found to be more effective than stem and root extracts. While the total content
of phenols and flavonoids were found high in leaves and fruit extracts.[153] The aqueous
www.ejpmr.com
339
Sharma et al. European Journal of Pharmaceutical and Medical Research
extract from the leaves of the P. minima was evaluated to study the in vitro antioxidant
activity. Two methods viz. DPPH radical scavenging assay and nitric oxide scavenging assay
were used to check antioxidant activity of the plant leaves. The results indicated that aqueous
extract of leaves of P. minima is effective in scavenging free radicals and has the potential to
be a powerful antioxidant.[154] The methanolic extract and chloroform fraction of P. minima
(L.) were used to investigate the anti-inflammatory, analgesic and anti-pyretic activity in
NMRI mice and Wistar rats. Both crude extract and chloroform fraction showed remarkable
anti-inflammatory and analgesic activities. The anti-pyretic activity was checked against
Brewer‟s yeast fever model, both extracts were insignificant.[155] The work by Chang et al.
demonstrated the anti-oxidant activity of P. peruviana (L.) aqueous extract and its
hepatoprotective effects in rats. This study concludes that the water extract possesses anti-
oxidant activity and potent hepatoprotective effect against acetaminophen induced liver
injury in rats.[156] The anti-oxidant, total flavonoid, phenolic anti-inflammatory activities of
different extracts of P. peruviana were also analyzed. The superficial carbon dioxide (SFe-
CO2) method was used to prepare the three extracts (SCEPP-0, SCEPP-4 and SCEPP-5).
These extracts were compared against the aqueous and ethanolic extracts of P. peruviana.
The different extract concentration showed the positive results against the tested activities[157]
Sue-Jing Wu and co-workers, worked on the anti-oxidant activity of the P. peruviana, the hot
water and ethanol extracts were prepared in the different concentration of 20, 40, 60, 80 and
95% from the whole plant. Results obtained show that at 100µg/mL, the 95% ethanolic
extract exhibit most potent inhibition rate on FeCl2-ascorbic acid induced lipid proliferation
in rat liver homogenate. The ethanolic extract shows a very significant and stronger anti-
oxidant activity than α-tocoferol and hot water extract. These studies conclude that ethanolic
extract have a very potent anti-oxidant activity and the extract with 95% of ethanol possesses
highest anti-oxidant activities.[158]
Ethnobotanical Aspects: Traditional uses of P. angulata leaves showed that herb is used to
reduce spleen, liver and bladder inflammations. The whole cooked plant is used in baths for
inflammatory processes like rheumatism. Its juice is used as a sedative, depurative, anti-
rheumatic and for earache in Amazon valley.[159] In Taiwan, it is used in the medicine
preparation of diabetes, malaria and asthma.[160] The rural people of Peruvian Amazon uses
the leaves for problems related to malaria, liver and hepatitis.[161, 162] The herb is used in
Western Africa as a traditional treatment of cancer.[163] The fruit and aerial parts of the plant
are used in the treatment of boils, sores or wounds, constipation and digestive problems.[164]
www.ejpmr.com
340
Sharma et al. European Journal of Pharmaceutical and Medical Research
P. alkekengi is distributed and used in Asia (Iran, India, Japan and china) and Europe (Spain,
Italy and Turkey) but not much used in modern practices.[165] It is also used in Iranian herbal
medicine for curing the disease related microbes, urinary tract, kidney and bladder stones.[166]
This plant possesses multiple traditional uses, in Colombia the fruit juice of the plant used for
the treatment of „pterygium‟. Traditional uses of the herb P. longifolia is extensively reported
as medicine, the Omaha and Ponca tribes generally using the “crooked medicine” to treat
headache, stomach problems and to dress wounds.[33, 110] P. minima is diuretic, laxative and
appetizing bitter tonic used in inflammations, antigonorrheic, enlargement of the spleen and
abdominal troubles.[167-169] The fruits and flowers of the plant used in the stomach pain,
constipation and herb paste is used in ear problems.[170] Traditionally P. ixocarpa fruit juice is
used as eyewash and in Guatemala the plant juice is used to cure for the respiratory and
gastrointestinal problem.
CONCLUSION
The species Physalis is widely available as weed and is cultivated for differnt purposes like,
medicinal, food, forage, ornamental and other usages. The manifestations can be made on the
basis of this comprehensive perusal of literature, that the Physalis spp. are being used
traditionally, due to their immense therapeutic potential to treat/cure various diseases. The
species is a rich source of bioactive compounds like, physalins, secosteroids, and
withanolides etc. with wide range of health benefits. Cytomorphological data reveals that
there is an immense need to find out new cytomorphotypes for further germplasm
maintenance and evaluation, because till today no body is working on these important
aspects. As per reported phytochemical data, it is concluded that there is a need to identify
few more chemotypes for further herbal and allopathic drugs formations. There is huge need
and possibilities to isolate new active components from untouched species of the genus
Physalis from India. Many studies demonstrated significant anti-inflammatory, anti-cancer,
anti-asthmatic, anti-diabetic and anti-bacterial activities etc. which are reported in the extracts
of different parts and from its phytoconstituents. As per the recorded data it is cleared that six
species have been extensively studied on different parameters but need to do further
extensive bioactivities on these species. The various existed therapeutic methods to treat
rheumatoid arthritis and other immunological disorders, having lots of future possibilities.
Different studies and investigations showed that, these plant species mainly involved in the
immunological effects. Thus, evidences promising drug therapy for immunological disorders.
These pharmacological activities and identified compounds provide solid scientific evidence
www.ejpmr.com
341
Sharma et al. European Journal of Pharmaceutical and Medical Research
for some of the traditional therapeutically claims. A variety of phytoconstituents has been
isolated from the different parts of various species. Thus, there remains a very wide scope for
further scientific exploration of Physalis spp. to establish their therapeutic efficacy and
commercial exploitation. Further it is the first constructive, concise and seemed to be more
important review article for the genus Physalis (L.) from Indian origin, which will definitely
help researchers from India and abroad.
ACKNOWLEDGEMENT
The authors are grateful to His Holiness Baba Iqbal Singh Ji President, The Kalgidhar Trust
& Founder Chancellor of Eternal University (H.P.), Hon‟ble Vice Chancellor, Eternal
University, Baru Sahib (Himachal Pradesh) India and former Head, Dr. R. C. Gupta,
Department of Botany, Punjabi University, Patiala (Punjab) India for providing necessary
facilities and logistic support for carrying out the study.
REFERENCES
1. Ahmad I, Aquil E, Ahmad F, Owis M. Herbal medicines: prospects and constrains in
modern phytomedicine, Turning medicinal plants into drugs: Wiley-Vch; 2006.
2. Shirwaikar A, Verma R, Lobo R, Shirwaikar A. Phyto-therapy aspects: Natural Product
Radiance 2009; 8(1): 55-63.
3. Agbor G, Talla L, Ngogang J. Toxicity of herbal preparations. Cam. J. Ethanobot
2005; 1: 23-28.
4. Aquil F, Ahmad I, Mehmood Z. Antioxidant and free radical scavenging properties of
twelve traditionally used, Indian medicinal plants. Turk J Biol 2006; 30: 177-183.
5. Nirmala A, Manju P, Lalitha G. Phytochemical screening of Plumeria rubra and their
antioxidant activities. 2009; 6(9): 4-7.
6. Jose A, Therezinha T, Deise X, Ivone R, Melissa S, Zenildo F. Molluscicidal activity of
Physalis angulata L. extracts and fractions on Biomphlaria tenagohpila under laboratory
condition. Mem Inst. Oswaldo Cruz. 2003; 98(3): 425-428.
7. Deb B. Solanaceae in India. In: Hawkes J, Lester R, Skelding A. The biology and
taxonomy of solanaceae. Academic press, London; 1979: 3-48.
8. Vatsavaya R, Reddy C, Rajarao K. The myth of “minima” and “maxima,” the species of
Physalis in the Indian subcontinent. Acta Phytotaxonomica Sinica 2007; 45(2): 239-245.
9. Pogan, E., Jankun A, Wcis1lo H. Further studies in chromosome numbers of Polish
angiosperms. Part XXI.Acta Biol. Cracov 1989 ; 30: 119136.
www.ejpmr.com
342
Sharma et al. European Journal of Pharmaceutical and Medical Research
10. Badr, A, Khalifa S, Aboel I, Abou M. Chromosomal criteria and taxonomic relationships
in the Solanaceae. Cytologia 1997; 62: 103113.
11. Kliphuis E, Wieffering J. In IOPB chromosome number reports LXIV. Taxon
1979; 28: 398400.
12. Yang D, Zhou J. Chromosome studies of 7 medicinal plant species. Guihaia 1998; 18(2):
115118.
13. Lydia, G, Rao K. A new cytotype of Physalis angulata L. Chromosome Inf. Serv 1982;
32: 34.
14. Husaini H, Iwo G. Cytomorphological studies in some weedy species of the family
Solanaceae from Jos Plateau, Nigeria. Feddes Repert 1990; 101: 4147.
15. Ganapathi A, Sudhakaran S, Kulothungan S. The diploid taxon in Indian natural
populations of Physalis L. and its taxonomic significance. Cytologia 1991; 56: 283288
16. Venkateswarlu J, Rao K. Morphology of the pachytene chromosomes of Physalis
angulata. Cytologia 1979A; 44: 557560.
17. Pedrosa, A. Citogenética de angiospermas coletadas em Pernambuco V. Acta Bot
1999; 13(1): 4960.
18. Tuteja S, Bhatt R. Chromosome number reports LXXXV. Taxon 1984; 33: 756760
19. Hinton W. The systematics of Physalis pumila ssp. hispida (Solanaceae). Syst. Bot 1976;
1: 188193.
20. Bir S, Kumari S, Shoree S, Sagoo M. Cytological studies in certain bicarpeilatae from
north and central India. J. Cytol. Genet. 1978; 13: 99106.
21. Bir S, Kumari S, Shoree S, Sagoo M. Cytological studies in certain bicarpeilatae from
north and central India. J. Cytol, Genet. 1978A; 13: 99106.
22. Kumar J, Kumar A, Sinha. Influence of distributional pattern on the reproductive
mechanism and recombination system of solanaceous weeds. Glimpses Cytogenet. India
1989; 2: 6267.
23. Gupta S, Roy S. A modified technique for the classification of somatic chromosomes.
Curr. Sci. 1981; 50: 423424.
24. Shibata K. Estudios citologicos de plantas colombianas silvestres y cultivadas. J. Agric.
Sci. Tokyo 1962; 4962.
25. Panda R, Rao K. Spontaneous chromosome fragmentation in cape gooseberry Physalis
peruviana L. Cell Chromosome Res 1983; 6: 910.
26. Rao K. Morphology of the pachytene chromosomes of tomatillo (Physalis ixocarpa
Brot.). Indian J. Bot. 1979; 2: 209213.
www.ejpmr.com
343
Sharma et al. European Journal of Pharmaceutical and Medical Research
27. Quiros F. Overview of the genetics and breeding of husk tomato. Hort. Sci. 1984; 19:
872874.
28. Lydia G, Rao K. Spontaneous desynapsis in tomatillo (Physalis ixocarpa Brot.). J. Cytol.
Genet. 1981; 16: 197201.
29. Bastos T, Silveira A, Salgado G, Picanco W, Nascimento M. Physalis angulata extracts
exerts anti-inflammatory effects in rats inhibiting different pathways. J
Ethnopharmacology 2008; 118: 251-264.
30. Mahalakshami A, Nidavani R. Physalis angulata L.: An ethanoparmacological review.
Indo American Journal of Pharmaceutical Research 2014; 4(03): 1479-1486.
31. Tapia M, Fries A. Guia de campo de los cutivos andinos. Lima: FAO y ANPE Valenzuela
A & Ronco A (2004). Fitoesterols y fitoestanoles: aliados naturales para la proteccion de
la salud cardiovascular. Revista Chilena de Nutrition 2007; 21(1): 161-169.
32. Puente L, Pinto-Munoz C, Castro E, Cortes M. Physalis peruviana Linnaeus, the multiple
properties of a highly functional fruit: A review. Food Research International 2011; 44:
1733-1740.
33. Kindscher K, Long Q, Corbett S, Bosnak K, Loring H, Cohen M, Timmermann. The
ethnobotony and ethnopharmacology of wild tomatillos, Physalis longifolia Nutt., and
related Physalis Species: A review. Economic Botony XX(X) 2012; 1-13.
34. Patel T, Shah K, Jiwan K, Shrivastava N. Study on the antibacterial potential of Physalis
Minima Linn. Indian J Pharm Sci. 2011; 73(1): 111115.
35. Compedium of medicinal plants used in Malayasia, Herbal Medicine research center ,
Institute for Kualalumpur 2002; 2: 221.
36. The wealth of India: A dictionary of Indian raw material and industrial products- Raw
material series, publications and information directorate, CSIR, New Delhi 1969; Vol. 8:
37-38; First suppl series CSIR-NISCAR. New Delhi; vol. 4 (J-Q): 307-308.
37. Kirtikar K, Basu B. Indian medicinal plants. 2008; 3: 1766-1767.
38. Pandey C. Medicinal plants of Gujarat, Gujarat ecological educational and research
foundation, Gujarat, India. 2005: 387.
39. Khare C. Indian medicinal plants: an illustrated dictionary. Springer 2007: 483.
40. Parmar C, Kaushal M. Physalis minima, In: Wild fruits. Kalyani Publishers; New Delhi,
India, 1982: 62-65.
41. Lavie D, Glotter E, Shvo Y. Constituents of Withania somnifera Dun. III. The side chain
of withaferin A. Journal of Organic Chemistry 1965; 30: 17741778.
www.ejpmr.com
344
Sharma et al. European Journal of Pharmaceutical and Medical Research
42. Pintea A, Varga A, Stepnowski P, Socaciu C, Culea M, Diehl H. Chromatographic
analysis of carotenol fatty acid esters in Physalis alkekengi and Hippophae rhamnoides.
Phytochem Anal 2005; 16: 188-195.
43. Qiu L, Zhao F, Jiang Z, Chen L, Zhao Q, Liu H, et al. Steroids and flavonoids from
Physalis alkekengi var. franchetii and their inhibitory effects on nitric oxide production. J
Nat Prod 2008; 71: 642-646.
44. Sen G, Pathak D. Physalin L, a 13, 14 seco-16, 24 cytosteroid from Physalis minima.
Phytochemistry 1995; 39: 1245-1246.
45. Leong K, Muhammad T, Sulaiman F. Ctotoxic activities of Physalis minima L.
Choloroform extract on human lung adenocarcinoma NCL-H23 cell lines by induction of
apoptosis. Evid Based Complement Alternat Med 2011: 185064.
46. Rao C, Lakshminarayana G, Prasad L, Rao M, Azeemoddin G, Ramayya A and Rao T.
Characteristics and compositions of Carissa spinarum, Leucaena leucocephala and
Physalis minima seeds and oils. J Amer Oil Chem Soc 1984; 61(9): 1472-1473.
47. Sinha C, Ali A, Bagchi A, Shai M, Ray A. Physalindicanols, new biogenetic precursors of
C28-steroidal lactones from Physalis minima var. indica. Planta Med 1987; 53(1): 55-57.
48. Shubash S, Anil R, Yoshiteru O, Anjana B, Hiroshi H. Withaphysalin E, a withanolide of
Physalis minima var. indica. Phytochemistry 1987; 26(7): 2115-2117.
49. Kirson I, Zaretskii Z, Glotter E. Withaphysalin C, a naturally occurring 13, 14-seco-
steroid. J Chem Soc: 1976, pp. 1244-1247.
50. Sahai M, Kirson I. Withaphysalin D, a new withaphysalin from Physalis minima Linn.
Var. indica. J Nat Prod 1984; 47(3): 527-529.
51. Champan, Hall. Dictionary of organic compounds, American Chemical Society.
Chemical Abstracts Service 1996; 9: 6490.
52. Atta ur-Rehman, Studies in natural products chemistry: bioactive natural products, part
L. Gulf Professional Publishing Science; 2005: 1022-1026.
53. Schmelzer H, Gurib-Fakim A. Medicinal plants, plant resources of tropical Africa
(Program). PROTA 2008; 440.
54. Glotter E, Kirsol I, Abraham A, Sethi D, Suramanian S. Steroidal constituents of Physalis
minima (Solanaceae). J Chem Soc Perkin 1975; 14: 1370- 1374.
55. Choudhary I, Yusuf S, Yasmeen K, Atta-Ur-Rahman. Antileishmanial physalins from
Physalis minima. Nat Prod Res 2007A; 21(10): 877-883.
56. Choudhary I, Yousaf S, Samreen, Ahmed S, Atta-Ur-Rehman. New leishmanicidal
physalins from Physalis minima. Nat Prod Res 2007B; 21(10): 877-883.
www.ejpmr.com
345
Sharma et al. European Journal of Pharmaceutical and Medical Research
57. Waterfall T. A taxonomic study of genus Physalis in North America north of Maxico.
Rhodora 60; 1958: 107-114. 128-142.
58. Waterfall T. Physalis in Maxico, Central America and the West indies,” Rhodora 60;
1967: 82-120, 203-239, 319-329.
59. D‟Arcy G. The classification of Solanaceae. In: Hawkes H, Lester R, Skelding A. The
biology and taxonomy of solanaceae. London; Academic press; 1979: 3-48.
60. D‟Arcy G. The Solanaceae since 1976, with a review of its biogeography. In Hawkes H,
Lester R, Nee M, Estrada N. Solanaceae III: Taxonomy- chemistry-evolution. Kew;
Royal Botanic Gardens, Kew; 1991: 75-137.
61. Rydberg A. The North American species of Physalis and related genera. Memoirs of the
Torry Botanical Club 1896; 4: 297-372.
62. Menzel Y. The cytotaxonomy and genetics of Physalis. The proceedings of American
Philosophical Society 1951; 95 (2):132-183.
63. Vasina E, Maslennikova A, Abubakirov K. Physalis withasteroids. Khim Priord Soed
1986; 3: 243-255.
64. Glotter E. Withanolides and related ergostane-type steroids. Nat Pro Rep 1991; 8:
415-440.
65. Makino B, Kawai M, Ogura T, Nakanishi M, Yamamura H, Butsugan Y. Structural
revision of physalin H isolated from Physalis angulata L.,” J. Nat. Prod 1995; 58: 1668-
1674.
66. Tomassini B, Barbi N, Ribeiro I, Xavier D. Genero Physalis-Uma revisao sobre
vitaesteroides. Quimica Nova 2000; 23: 47-57.
67. Gottlieb E, Cojocaru M, Sinha C, Saha M, Bagchi A, Abid A, Ray A. Withaminimin a
withanolide from Physalis minima. Phytochemistry 1987; 26(6): 1801-1804.
68. Basey K, McGaw A, Woolley G. Phygrine, an alkaloid from Physalis species.
Phytochemistry 1992; 31(12): 4173-4176.
69. Sen G, Pathak D. Physalin L, a 13, 14-seco-16, 24 cyclosteroid from Physalis minima
Phytochemistry 1995; 3(5): 1245-1246.
70. Kawai M, Makino B, Yamamura H, Butsugan Y. Upon „Physalin L‟ isolated from
Physalis minima. Phytochemistry 1996; 43(3): 661-663.
71. Ng Ang Ser. Flavonoids from Physalis minima. Phytochemistry 1988; 27(11):
3708-3709.
www.ejpmr.com
346
Sharma et al. European Journal of Pharmaceutical and Medical Research
72. Koh L, Ng S. Structures of two flavonoids from Physalis minima, 5-methoxy-6, 7-
methylenedioxyflavone (I) and 5, 6, 7-trimethoxyflavone(II). Acta Cryst 1993; C49:
105-107.
73. Subramanian, Shankar S, Sethi D. Bitter principles of Physalis minima and Physalis
peruviana. Curr Sci 1971; 40: 85-86.
74. Mericli F. Bilimsel acidan altin cilek meyveleri (Physalis peruviana). Fitomed
2011; 20: 18-22.
75. Ramadan M. Bioactive phytochemicals, nutritional value and functional properties of
cape gooseberry (Physalis peruviana): an overview. Food Research International
2011; 44; 7: 1830-1836.
76. Rodrigues E, Rockenbach I, Cataneo C, Gonzaga V, Chaves E, Fett R. Minerals and
essential fatty acids of the exotic fruit Physalis peruviana L. Food Science and
Technology 2009; 29(3): 642-645
77. Valdenegro M, Henriquez C, Lutz M, Almonacid S, Simpson R. Drum dried, liophylized
dried and traditional drying of golden berry (Physalis peruviana L.): effects in nutritional
and healthy quality. In proceedings of the International Conference On Food Innovation,
Food Innova, Valencia, Calif, USA; 2010.
78. Yen C, Chiu C, Chang F, Chen J, Hwang C, Hseu Y, Yanng H, Lee A, Tsai M, Guo Z,
Cheng Y, Liu Y, Lan Y, Chang Y, Co Y, Chang H, Wu Y. -hydroxywithanolide E
from Physalis peruviana (golden berry) inhibits growth of human lung cancer cells
through DNA damage, apoptosis and G2/M arrest. BMC Cancer 2010; 10(46): 1-8.
79. Wu S, Ng L, Lin D, Huang S, Wang S, and Lin C. Physalis peruviana extract induces
apoptosis in human Hep G2 cells through CD95/CD95L system and the mitochondrial
signaling transduction pathway. Cancer Lett 2004; 215: 199-208.
80. Cassady J, Suffness M. Terpenoid antitumor agents, in anticancer agents based on natural
products. Cassady J, Douros J, Eds. Academic Press 1980: 201-269.
81. Dinam L, Sarker S, Sik V. 28-hydroxywithnolide E from Physalis peruviana,”
Photochemistry 1997; 44: 509-512.
82. Zhang H, Samadi A, Gallaghar R, Araya J, Tong X, Day V, Cohen M, Kindscher K,
Gollapudi R, Timmermann B. Cytotoxic withanolide constituents of Physalis longifolia.
J. Nat Prod 2011; 74 (12): 2532-2544.
83. Samadi K, Bazzill J, Zhang X, Gallagher R, Zhang H, Gollapudi R, Kindscher K,
Timmermann B, Cohen M. Novel withanolides target medullary thyroid cancer through
www.ejpmr.com
347
Sharma et al. European Journal of Pharmaceutical and Medical Research
inhibition of both RET phosphorylation and the mammalian target of rapamycin pathway.
Surgery 2012; 152(6): 1238-1247.
84. Zhang H, Samadi A, Cohen M, Timmermann B. Pure Appl. Chem 2012; 84: 1353-1367.
85. Kelly K, Quinn L, Steve C, Kirsten B, Hillary L, Mark C, Barbara T. The
ethnopharmacology of wild tomatillos, Physalis longifolia Nutt, and related Physalis
species: a review. Economic Botany 2012; 20(10): 1-13.
86. Lijuan S, Jianwen L, Ping L, Youjun Y, Lei M, Lihong H. Immunosuppression effect of
withangulatin A from Physalis angulata via heme oxygenase 1-dependent pathways.
Process Biochemistry 2011; 46: 482-488.
87. Ismail N and Alam M. A noval cytotoxic flavonoid glycoside from Physalis angulatae.
Fitoterapia 2001; 72(6): 676679.
88. Elisalva G, Milena L, Luana S, Ivon R, Therezinha C, Ricardo S, Washington S, Milena
S. Activity of physalins purified from Physalis angulata in in-vitro and in vivo models of
cutaneous leishmaniasis. Journal of Antimicrobial Chemootherapy 2009; 64: 8487.
89. Choi k, Murillo G, Su B, Pezzuto J, Kinghorn A, Mehta R. Ixocarpalactone A isolated
from the Maxican tomatillo shows potent antiproliferative and apoptotic activity in colon
cancer cells. FEBS Journal 2006; 273: 5714-5723.
90. Todd. Martindales: The extra pharmacopeia: 1985.
91. Todd. Martindales: The extra pharmacopeia :1993.
92. Zaki Y, El- Alfy T, Gohary E. Study of withanolides, physalins, antitumor and
antimicrobial activity of Physalis peruviana L. Egyptian Journal of Pharmacological
Science 1987; 28: 235-245.
93. Chiang C, Jaw S, Chen C, Kan W. Antitumor agent, physalin F from Physalis angulata L.
Anticancer Research 1992A; 12: 837-844.
94. Chiang C, Jaw S, Chen P. Inhibitory effects of physalin B and physalin F on various
human leukemia cells in vitro. Anticancer Research 1992B; 12: 1155-1162.
95. Bastos G, Santos A, Ferreira V, Costa A, Bispo C, Silveira A, Nascimento J.
Antinociceptive effect of the aqueous extract obtained from roots of Physalis angulata L.
on mice. Journal of Ethnopharmacology 2005; 103: 241-245.
96. Hseu C, Wu R, Chang W, Kumara S, Linb K, Huang Y, Lee Z, Hsieh T, Chung G, Wang
M, Yang L. Inhibitory effects of Physalis angulata on tumor metastasis and angiogenesis.
Journal of Ethnopharmacology 2011; 135: 762-771.
www.ejpmr.com
348
Sharma et al. European Journal of Pharmaceutical and Medical Research
97. Vessal M, Mehrani H, Omranni G. Effects of an aqueous extract of Physalis alkekengi
fruit on estrus cycle, reproduction and uterine creatin kinase BB-isozyme in rats. Journal
of Ethanopharmacology 1991; 34: 69-78.
98. Vessal M, Yazdanian M. Comparision of effects of an aqueous extract of Physalis
alkekengi fruits and/or various doses of 17-β-estradiaol on rat estrous cycle and uterine
glucose 6-phosphate dehydrogenase activity. Comparative Biochemical Physiology
1995A; 112(2): 229-236.
99. Vessal M, Mostafavi Z, Kooshesh. Age and sex dependence of the effects of effects of an
aqueous extract of Physalis alkekengi fruits on rat hepatic glucose 6-P dehydrogenase
activity. Comparative Biochemical Physiology 1995B; 111(4): 675-680.
100. Vessal M, Rasti, Kooshesh. Modulation of pituitary and basomedial hypothalamic lysyl-
aminopeptidase activities by β-estradiol and/ or an aqueous extract of Physalis alkekengi
fruits. Comparative Biochemical Physiology 1996; 115(2): 267-271.
101. Chopra C. Glossary of Indian medicinal plants. Council of Scientific and Industrial
Research, New Delhi: 1956.
102. Roddick G. The importance of solenaceae in medicine and drug therapy. In solenaceae
III. Whitstable Litho Ltd, Withstable, Kent: 1991.
103. Agarwal S. Drug plants of India vol. II. New Delhi; Kalyani Publishers: 1997.
104. Dornberger.K. The potential antineoplastic acting constituents of Physalis alkekengi L.
var francheii Mast. Die Pharmazie 1986; 41: 265-268.
105. Grzybek, J.K.S. Potential and new cancerostatics of plant origion. Parm. Pol 1986; 38
106. Purushothaman K, Vasanth S. Chemistry and pharmacology of steroids derivatives from
Physalis. Journal of Scientific and Industrial Research 1977; 47: 326-334.
107. Jain P, Puri H. Ethnomedicinal plants of Jaunsar-Bawar hills, Uttar Pradesh, India.
Journal of Ethnopharmacology 1984; 12: 213-222.
108. Das D, Agarwal V. Fruit drug plants of India. New Delhi; Kalyani Publishers: 1991
109. Warrier P, Nambiar V, Ramakutty C. Indian medicinal plants, a compendium of 500
species Kottakkal. Orient Longman Limited; 1995: Vol 4.
110. Glimore R. Uses of plants by the Indians if the Missouri river region; University of
Nebraska Press; Lincoln: 1977.
111. Kindscher K, Long Q , Corbett S, Bosnak, Loring H, Cohen M, Timmermann B. The
ethnobotany and Ethnopharmacology of wild tomatillos, Physalis longifolia Nutt. and
related Physalis species: a review. Economic Botony 2012; 66(3): 298-310.
112. Garcia Barriga H. Floura medicinal de Colombia. Imprenta Nacional 1975; 383-384.
www.ejpmr.com
349
Sharma et al. European Journal of Pharmaceutical and Medical Research
113. Wong W. A hypothesis on the pathogenesis of pterygiums. Ann Ophthalmol 1978; 10:
303-308.
114. Sanchooli N. Antidiabetic properties of Physalis alkekengi extract in alloxan-induced
diabetic rats. Research Journal of Pharmaceutical, Biological and Chemical Sciences
2011; 2(3): 168.
115. Lin Y, Chiang H, Kan W, Home E, Shih S, Won M. Immunomodulatory activity of
various fractions derived from Physalis angulata L. extract. The American Journal of
Chinese Medicines 1992; 20.
116. Bastos G, Santos A, Ferreira V, Costa A, Bispo C, Silveira A, Nascimento J.
Aminociceptive effect of the aqueous extract obtained from roots of Physalis angulata L.
on mice. Journal of Ethnopharmacology 2006; 103: 241-245.
117. Sharma A, Chakraborti, Handa. Anti-hepatotoxic activity of some Indian herbal
formulations as compared to silmarin. Fitoterapia 1991; 62: 229-235.
118. Ahmed L. Renoprotective effect of Egyptian cape gooseberry fruit (Physalis peruviana
L.) against acute renal injuries in rats. The Scientific World Journal, Hindawi Publishing
Corporation 2014.
119. Pratheeba M, Umaa K, Ramesh B. Hepatoprotective activity of Physalis minima against
paracetomal induced hepatic damage in rats. Int. J. Curr. Res. Biosci. Plant Biol 2014;
1(1): 61-69.
120. Gengaihi E, Hassan E, Hamed A, Zahran G, Mohammed A. Chemical composition and
biological evaluation of Physalis peruviana root as hepato-renal protective agent. J Diet
Suppl 2013; 10(1): 39-53.
121. Arun M and Asha V. Preliminary studies on antihepatotoxic effect of Physalis peruviana
Linn. (Solanaceae) against carbon tetrachloride induced acute liver injury in rats. Journal
of Ethnopharmacology 2007; 111(1): 110-114.
122. Shu-Jing W, Lean-Teik N, Ching-Hsein Ch, Doung-Liang L, Shyh-Shyan W, Chun-
Ching L. Antihepatoma activity of Physalis angulata and Physalis peruviana extracts and
their effects on apoptosis in humen Hep G2 cells. Life Sciences 2004; 74: 2061-2073.
123. Kumar S, Kishor G, Sindhu priya S. In vitro anti-inflammatory and anti-arthritic activity
of leaves of Physalis angulata L Int. J. & Ind. Res 2011; 1(3): 211-213.
124. Juan P, Marta F, Luis O, Lady E. Determining the pharmacological activity of Physalis
peruviana fruit juice on rabbit eyes and fibroblast primary cultures,” IOVS, 2008; 49(7):
3074-3079.
www.ejpmr.com
350
Sharma et al. European Journal of Pharmaceutical and Medical Research
125. Franco A, Matiz E, Calle J, Pinzón R, Ospina F. Anti-inflammatory activity of extracts
and fractions obtained from Physalis peruviana L. calyces. Biomedica 2007; 27(1):
110-115.
126. Milena B, Moema B, Ivone M, Therezinha C, Ricardo R. Inhibition of macrophage
activation and lipopolysaccharides-induced death by seco-steroids purified from Physalis
Angulata L. Eur J Pharmacol 2011; 459: 107-112.
127. Lin Y, Chiang H, Kan W, Hone E, Shih S, Won M. Immunomodulatory activity of
various fractions derived from Physalis angulata L extract. Am J Chin Med 1992; 20
(3-4): 233-243 .
128. Sateesh P, Porika R and Mamidala E. Phytochemical analysis and in vitro antidiabetic
activities of Physalis angulata fruit extracts.Phytochemical Analysis and In vitro
Antidiabetic 2014; 5(2): 34-38.
129. Kasali F, Kadima J, Mpiana P, Ngbolua K, Tshibangu D. Assessment of antidiabetic
activity and acute toxicity of leaf extracts from Physalis peruviana L. in guinea- pig.
Asian Pacific Journal of Tropical Biomedicine 2013; 3(11): 841-846.
130. Suchitra E, Estari M. Evaluation of antidiabetic activity of medicinal plant extracts used
by tribal communities in rural areas of Warangal district, Andhra Pradesh, India. Biology
and Medicine 2013; 5: 20-25.
131. Abo K, Lawal.I, Antidiabetic activity of Physalis angulata extracts and fractions in
alloxan-induced diabetic rats. Journal of Advanced Scientific Research 2013; 4(3); 32-36
132. Oladele M, Ode J, Akande G, Ogunbodede M, Simon K. Effects of ethanolic root
extracts of Physalis angulata on alloxan induced Diabetic rats. Int.J.A.PS.BMS, 2013;
2(2): 095-100.
133. Ngern M ,Youn U , Park E , Kondratyuk T , Miklossy G , Simmons C , Turkson J,
Pezzuto J, Chang L. Anticancer potential of Physalis peruviana (Poha). Planta Med 2013;
79: 13.
134. Ying Wu S, Lii Leu Y, Ling Chang Y, Shung Wu, Chung Kuo P, Ren Liao, Ming Teng,
C, Lin Pan S. Physalin F Induces cell apoptosis in human renal carcinoma cells by
targetting NF-kappaB and generating reactive oxygen species. PlusOne 2012;7(7): 1-10.
135. Yu Yen C, Chih Chiu C, Rong Chang F, Fu Chen J, Ching Hwang, Cheng Hseu Y, Ling
/Ching Chang Y, Chin Ko Y, Chang H, Wu Y. -hydroxywithanoide E from Physalis
peruviana (golden berry) inhibits growth of human lung cancer cells through DNA
damage, apoptosis and G2/M arrest. BMC Cancer 2010; 10; 46: 1-8.
www.ejpmr.com
351
Sharma et al. European Journal of Pharmaceutical and Medical Research
136. Nathiya M and Dorcus. Preliminary phytochemical and anti-bacterial studies on Physalis
minima Linn. INT J CURR SCI 2012: 24-30.
137. Donker A, Glover R, Boateng J, Gakpo V. Antibacterial activity of the fruit extract of
Physalis angulata and its formulation. Journal of Medical and Biomedical sciences 2012;
1(4): 21-26.
138. Parvin T, Pourdad P. Evaluation of antifungal activity of Physalis alkekengi L. extracts
on Microsporum canis, Candida albicans, Trichophyton mentagrophytes and Nocardia
asteroids. American-Eurasian J. Agric. & Environ. Sci. 2011; 11(6): 863-866.
139. Osho A, Adetunji T, Fayemi O, Moronkola O. Antimicrobial activity of essential oils of
Physalis angulata L. Afr J Tradit Complement Altern Med. 2010; 7(4): 303-306.
140. Helvac S, Kokdil G, Kawai M, Duran N, Duran G, Guvenç A. Antimicrobial activity of
the extracts and physalin D from Physalis alkekengi and evaluation of antioxidant
potential of physalin D. Pharm Biol 2010; 48(2): 142-150.
141. Shariff N, Sudarshan, M, Umesha S, Hariprasad P. Antimicrobial activity of Rauvolfia
tetraphylla and Physalis minima leaf and callus extracts. African Journal of
Biotechnology 2006; 5(10): 946-950.
142. Choudhary M, Yousuf S, Samreena, Ahmed S, Rahman A. New leishmanicidal
physalins from Physalis minima. Natural Product Research: Formerly Natural Product
Letters 2007; 21; 10: 877-883.
143. Choudhary I, Yousaf S, Ahmed S, Yasmeen K. Antileishmanial physalins from Physalis
minima. Chem biodivers 2005; 2(9): 1164-1173.
144. Jyothibasu T, Ramana K, Thalla S, Thalla S. Anti-asthamatic activity of alcoholic extract
of Physalis Angulata induced by ovalbumin. Am. J. PharmaTech Res 2012; 2(6):
1832-1834.
145. Jasem E, Javdan N. Study of analgesic activity of methanolic extracts of Physalis
Alkekengi in adult rats. Pharmacologyonline 2011; 3: 768-772.
146. Mohammad k, Gharib N, Maryam M, Zahra G, Naseri D. Antispasmodic effect of
Physalis alkekengi fruit extract on rat uterus. Iranian Journal of Reproductive Medicine
2008; 6(4): 193-198.
147. Santos J, Tomassini T, Xavier, Ribeiro M, Melissa S, Zenildo F. Molluscicidal activity
of Physalis angulata L. extracts and fractions on Biomphlaria tenagophila (d‟Orbigny,
1835) under laboratory conditions. Mem Inst Oswaldo Cruz, Rio de Janeiro, 2003; 98(3):
425-428.
www.ejpmr.com
352
Sharma et al. European Journal of Pharmaceutical and Medical Research
148. Kalsum U, Ali M, Widodo M, Kalim H. Effect of methanolic extract of Physalis minima
on gastric inflammation and gastric ulcers formation. Journal of Experimental and
Integrative Medicine 2013; 3(4): 331-335.
149. Jyothibasu T, Ramana K, Thalla S, Raju C. Diuretic activity of methanolic extract of
Physalis minima leaves. Scholars Research Library 2012; 4(6): 1832-1834.
150. Nanumala S, Kishore G, Chinnalalaiah R, Sriram C. Evaluations of diuretic activity of
methanolic extract of Physalis angulata L. leaves. International Journal of Pharmaceutical
Sciences Review & Research, 2012; 16: 2: 40.
151. Lusakibanzaa M, Mesiaa G, Tonaa G, Karemereb S , Lukukab A, Titsc M, Angenotc L,
Frédérichc M. In vitro and in vivo antimalarial and cytotoxic activity of five plants used
in Congolese traditional medicine. Journal of Ethnopharmacology 2010 ELSEVIER
152. Demir T, Ozen M, Kocabas E. Antioxidant and cytotoxic activity of Physalis peruviana
Medicinal Plant Research 2014; 4(3): 30-34.
153. Murali T, Vadluri R, Kumar M. In vitro determination of antioxidant activity of Physalis
angulata. International Journal of Pharma and Bio Sciences 2013; 4(3): 541-549
154. Kumar G, Shivalinge G, Umashankar N, Nandeesh R, Sreedhar S. In-vitro antioxidant
activity of aqueous extract of P. minima Linn. Research Journal of Pharmacology and
Phramacodynamics 2013; 2(5): 332-334.
155. Khan M, Khan H, Khan S, Mahmood T, Khan P, Jabar A. Anti-inflammatory, analgesic
and antipyretic activities of Physalis minima Linn. J Enzyme Inhib Med Chem, 2009;
24( 3): 632-637.
156. Chang J, Lin C, Wu S, Lin D, Wang S, Miaw C, Ng L, “Antioxidative and
hepatoprotective effects of Physalis peruviana extract against acetaminophen-induced
liver injury in rats. Pharmaceutical Biology 2008; 46; 10-11: 724-731.
157. Wu J, Tsai J, Chang S, Lin D , S.S. Wang , Huang S, Ng L. Supercritical carbon dioxide
extract exhibits enhanced antioxidant and anti-inflammatory activities of Physalis
peruviana. Journal of Ethanopharmacology 2006: 407-413.
158. Jing Wu S, Ng L, Huang Y, Lin D, Wang S, Huang S, Lin C. Antioxidant activities of
Physalis peruviana. Biol. Pharm. Bull 2005; 28(6): 963-966.
159. Lorenzi H. Plantas daninhas do Brasil. Nova Odessa, S~ao Paulo, Brasil 1982: 372.
160. Heish T, Huang Y, Lin Y, Chung G. Physalis angulata induced G2/M phase arrest in
human breast cancer cells. Food Chem Toxicol 2006; 44: 974-983.
161. Ferreyra R. Floura invasora de los cultivos de pacallpi y tingo Maria: 1970.
www.ejpmr.com
353
Sharma et al. European Journal of Pharmaceutical and Medical Research
162. Rutter A. Catalogo de plantas utiles de la Amazonia peruana instituto linguistico de
verano yarinacocha Peru: 1990.
163. Lawal O, Uzokwe E, Lgboanugo I, Adio F, Awuson A, Nwogwugwu, et al.
Ethnomedical information on collection and identification of some medicinal plants in
research institutes of South-west Nigeria. African J Pharm Pharmacol 2010; 4: 1-7.
164. Dokosi B. The herbs of Ghana. Ghana Uni-versities Press; Accra: 1998.
165. Unny R, Chauhan K, Jashi C. A review on potentiality of medicinal plants as a source of
new contraceptive principle. Phytomedicine 2003; 10: 233-260.
166. Dornberger K. The potential antineoplastic acting constituents of Physalis alkekengi L.
var francheii Mast. Die Pharmazie 1986; 41: 265-268.
167. Sinha C, Rey B. Chemical constituents of Physalis minima var. indica. J indian Chem
Soc 1988; 65: 740-741.
168. Yusuf M, Chowdhury U, Wahab A, Begum J. Medicinal plants of Bangladesh. BCSIR
Laboratories; Chittagong, Bangladesh: 1994.
169. Joy P, Thomas J, Mathew S, Skaria P. Medicinal plants Kerala Agriculture University,
aromatic and medicinal plants research station 1998: 195.
170. Vipin P, Ashok A. Traditional uses of ethnomedicinal plants of lower foot- hills. Indian J
Trad Knowledge 2010; 9(3): 519-521.
... The Chinese lantern has been recognized for centuries as a medicinal plant in the traditional medical practices of many countries, due to its anti-inflammatory, antibacterial, antiseptic, sedative, laxative, diuretic, hypoglycemic, spasmolytic, and other effects, as well as for the relief of malaria and syphilis symptoms [1,18,19]. In Chinese medicine, P. alkekengi (Physalis calyx seu Fructus) is a remedy for a number of diseasesfrom sore throat, eczemas, and rheumatism to hepatitis, urinary disorders, and tumors [1,2,10,14,18]. ...
... The Chinese lantern has been recognized for centuries as a medicinal plant in the traditional medical practices of many countries, due to its anti-inflammatory, antibacterial, antiseptic, sedative, laxative, diuretic, hypoglycemic, spasmolytic, and other effects, as well as for the relief of malaria and syphilis symptoms [1,18,19]. In Chinese medicine, P. alkekengi (Physalis calyx seu Fructus) is a remedy for a number of diseasesfrom sore throat, eczemas, and rheumatism to hepatitis, urinary disorders, and tumors [1,2,10,14,18]. In turn, Bulgarian folk medicine recommends the use of fresh or dried fruit for the treatment of liver diseases, combining hepatitis and ascites [3]. Dried fruits are also used as a painkiller for kidney and bladder stones, inflammations of the urinary tract, and hemorrhoids. ...
... P. alkekengi is also recognized as a functional food, being a rich source of valuable nutrients-vitamins A and C, minerals, unsaturated fatty acids, phenolics, phytosterols, and pectic substances [18,[20][21][22]. It should be noted that only fully ripened berries are suitable for consumption (unripe fruit and all aerial parts of the plant are toxic if swallowed), having a juicy texture, fresh flavor, and a slightly bitter taste, which normally disappears after fruit freezing. ...
Article
Full-text available
In recent years there has been an extensive search for nature-based products with functional potential. All structural parts of Physalis alkekengi (bladder cherry), including fruits, pulp, and less-explored parts, such as seeds and peel, can be considered sources of functional macro- and micronutrients, bioactive compounds, such as vitamins, minerals, polyphenols, and polyunsaturated fatty acids, and dietetic fiber. The chemical composition of all fruit structural parts (seeds, peel, and pulp) of two phenotypes of P. alkekengi were studied. The seeds were found to be a rich source of oil, yielding 14–17%, with abundant amounts of unsaturated fatty acids (over 88%) and tocopherols, or vitamin E (up to 5378 mg/kg dw; dry weight). The predominant fatty acid in the seed oils was linoleic acid, followed by oleic acid. The seeds contained most of the fruit’s protein (16–19% dw) and fiber (6–8% dw). The peel oil differed significantly from the seed oil in fatty acid and tocopherol composition. Seed cakes, the waste after oil extraction, contained arginine and aspartic acid as the main amino acids; valine, phenylalanine, threonine, and isoleucine were present in slightly higher amounts than the other essential amino acids. They were also rich in key minerals, such as K, Mg, Fe, and Zn. From the peel and pulp fractions were extracted fruit concretes, aromatic products with specific fragrance profiles, of which volatile compositions (GC-MS) were identified. The major volatiles in peel and pulp concretes were β-linalool, α-pinene, and γ-terpinene. The results from the investigation substantiated the potential of all the studied fruit structures as new sources of bioactive compounds that could be used as prospective sources in human and animal nutrition, while the aroma-active compounds in the concretes supported the plant’s potential in perfumery and cosmetics.
... Ex. DC.; P. longifolia Nutt.; P. minima L.; and P. peruviana L. (Sharma et al., 2015). ...
Article
Full-text available
Physalis, a diverse genus in the Solanaceae family, includes ground cherry and cape gooseberry. These plants thrive in various climates and regions worldwide, including India. They are valued for their edible fruits and significant medicinal properties. Modern research has identified secondary metabolites in Physalis, such as withaphysalins and physalins, which exhibit anti-cancer, anti-diabetic, and anti-inflammatory effects. Cape gooseberry is particularly rich in vitamins, minerals, and antioxidants. The medicinal uses of Physalis range from treating gastrointestinal issues, malaria, and skin conditions to anticancer and anti-diabetic applications. Extracts from Physalis demonstrate potent cytotoxicity against cancer cell lines and other therapeutic effects. Recent studies highlight its potential for treating various diseases like cancer and diabetes, as well as intriguing new applications in nutrition and medicine.
... The findings are in agreement with the previous studies showing that P. peruviana contains secondary metabolites; alkaloids, flavonoids, tannins, saponins, phenols, cardiac glycosides, terpenoids, and steroids [35,36], except for anthraquinones where we are reporting for its presence in P. peruviana leave extracts for the first time. Previous studies showed that many bioactive compounds have been isolated from the aerial parts of P. peruviana, such as phenolics, ticolidine, phytosterols [37], and various with anolides [38]. In the previous study by Maobe et al. [24], the presence of phytochemicals with various biological activities (alkaloids, saponins, steroids, terpenoids, tannins and flavonoids) was detected in aqueous extracts from Physalis peruviana leaves [24]. ...
Article
Full-text available
Bacterial resistance to the availably used antibiotics cause one of the greatest significant global health problems on both developed and developing countries due to factors such as inadequate sanitation, poor hygiene and overcrowded living conditions [1, 2]. With an escalating number of antibiotics resistance to high levels, the current study focused on scientific ideological search for an alternative to antibiotics by synergistic approach between Mondai whytei (MW) and Physalis peruviana (PP) that may be easily available, and provides efficient and cheap alternatives to antibiotics [3, 4]. The roots of Mondai whytei and the leaves of Physalis peruviana were shade-dried and ground into a fine powder which were then cold macerated with 70% ethanol for 48 h. Phytochemical screening of the ethanolic extract was conducted for the different types of phytochemicals. Minimum inhibitory concentrations (MIC) was determined against the two selected pathogens; S. aureus and E. coli with Chloramphenicol and Dimethyl sulfoxide (DMSO) used as the Positive and Negative controls respectively. A synergistic antibacterial interaction between Mondai whytei and Physalis peruviana extracts using Fractional inhibitory concentration indices (FICI). The results of the two ethanolic extracts of Mondai whytei and Physalis peruviana revealed that Alkaloids, flavonoids, tannins, saponins, phenols were found to be present. Cardiac glycosides, terpenoids, anthraquinnones and steroids were present only in ethanolic extract of Physalis peruviana leaves. But the present of anthraquinones in Physalis peruviana leaf extracts is being reported for the first time. The observed phytochemicals also showed an inhibitory activity on S. aureus and E. coli with MIC of 100 mg/mL and 0.5 mg/mL. However, synergistic extract had the lowest MIC comparable to that of the reference standard at p <0.05. The FICI were between 0.5 and 1.0. Therefore, MW:PP (1:1) gave an interesting better antibacterial activity against the two selected pathogens.
... As already stated, the identification of biologically active constituents in P. alkekengi tissues has been focused on fruit and calyces, as they are used in folk medicine, while phytochemical investigations of other plant parts (leaves, stems, roots) are rather scarce [29]. For those reasons, it is hard to make direct comparison between our results and published data, although some studies have identified similar chemical classes and individual volatile components in different P. alkekengi tissues, such as terpenoids, phenylpropanoids, aliphatic derivatives, organic acids, sucrose esters, and others [2,13,14,[30][31][32]. ...
Article
Full-text available
Physalis alkekengi L. (Solanaceae) is encountered in different regions of Bulgaria as a wild growing or ornamental plant. The objective of this work was to characterize the phytochemical composition (macro and micro components) of the leaves and stems of two local phenotypes (PA-SB and PA-NB), with the view of revealing their use potential. The dry leaves contained (DW) protein (16.25 and 19.27%), cellulose (25.16 and 25.31%), and ash (18.28 and 16.16%) and the stems contained protein (6.83 and 7.35%), cellulose (39.34 and 38.25%), and ash (15.01 and 7.48%) for PA-SB and PA-NB, respectively. The dominant amino acids (by HPLC) in the leaves of both phenotypes were arginine (21.3–22.3 mg/g) and aspartic acid (8.8–18.4 mg/g), and those in the stems were proline and aspartic acid for PA-SB (8.8, 7.7 mg/g); isoleucine and tyrosine for PA-NB (12.8, 6.6 mg/g). Mineral elements, determined by AAS (K, Ca, Mg, Na, Cu, Fe, Zn, Mn, Pb, Cr), also varied between phenotypes and plant parts. The leaves alone were further processed by extraction with n-hexane, for the identification of leaf volatiles (by gas chromatography-mass spectrometry). The analysis identified 28 components (97.99%) in the leaf extract of PA-SB and 32 components (97.50%) in that of PA-NB. The volatile profile of PA-SB leaves was dominated by diterpenes (49.96%) and oxygenated sesquiterpenes (35.61%), while that of PA-NB was dominated by oxygenated aliphatics (40.01%) and diterpenes (35.19%). To the best of our knowledge, the study provides the first data about the phytochemical composition of the leaves and stems of P. alkekengi from Bulgaria, in a direct comparison of phenotypes from two distinct wild populations, which could be of further scientific interest.
... ex Hornem., P. longifolia Nutt., P. minima L., P. peruviana L., P. virginiana Mill. (Sharma et al., 2015), and P. pruinosa L. (Singh and Pandey, 2002). State Rajasthan represents 4 species among 8 Indian species except for P. alkekengi, P. ixocarpa, P. longifolia and P. virginiana. ...
Article
Full-text available
The fruit and seed characteristic of Physalis peruviana L. and P. pruinosa L. were studied using fruit and seed colour, and shape along with dimensions and spermoderm pattern. The basic spermoderm sculpture was reticulate and mircro-reticulate in P. peruviana and P. pruinosa respectively. The epidermal cells of P. peruviana were large, irregular, non-isodiametric, and 08 - 15 gonals whereas in P. pruinosa small, irregular, and conjugate. Anticlinal boundaries of cells in P. peruviana observed sinuate, channeled, and thick while in P. pruinosa were straight to slightly sinuous and thin. Periclinal cell wall boundaries were observed as highly concave and straight to slightly concave in P. peruviana and P. pruinosa respectively. The study is useful for identification of both species by seeds.
... Genus Physalis terdiri dari 120 spesies yang terdistribusi di seluruh dunia, salah satunya adalah Physalis minima L. yang dikenal di Indonesia dengan nama ciplukan. 1 Daun ciplukan mengandung senyawa aktif antara lain fenolik (katekin, katekol, asam galat, asam elagik), alkana, aldehid, alkohol sekunder, asam amino, amina aromatik, dan senyawa halogen glikosida jantung, gula pereduksi, serta steroid sehingga disarankan digunakan sebagai alternatif herbal untuk berbagai penyakit. 2,3 Khasiat dari tanaman ini antara lain sebagai antioksidan, antibakteri, untuk terapi hipertensi dan diabetes yang dikombinasikan dengan tanaman obat lain. ...
Article
Many Indonesian people use plants for medicine and health care. In 2017, the Center for Research and Development of Medicinal Plants and Traditional Medicines (B2P2TOOT), the National Institute of Health Research and Development (Badan Litbangkes) conducted a Research on Medicinal Plants and Herbs (Ristoja) by collecting 30 types of medicinal plants. Physalis minima L. (ciplukan) is one of the Ristoja plants that has been studied at the Pharmaceutical Laboratory, Center of Health Research and Development of Biomedical and Basic Health Technology, Badan Litbangkes. This study aimed to determine the chromatogram profile of plants to obtain plant quality and clusters between plants from different geographic origins using chemometric applications. There were 66 ciplukan samples collected from 15 ethnic groups in 9 provinces in Indonesia. Analysis was performed using High Performance Liquid Chromatography (HPLC) with a Photo Diode Array (PDA) detector at a wavelength (λ) of 254 nm and 366 nm. From the optimization results, the HPLC eluent used was a mixture of acetonitrile and methanol with a gradient system. The results from HPLC were chemometrically processed with data interpretation using Principal Component Analysis (PCA). PCA results of HPLC chromatograms at λ 254 nm and 366 nm, showed 2 clusters, which indicated that Physalis minima L. Ristoja results had 2 phytochemical profiles. The peak detected at λ 366 nm was more complex than at λ 254 nm. Abstrak Masyarakat Indonesia banyak memanfaatkan tanaman untuk pengobatan maupun perawatan kesehatan. Pada tahun 2017, Balai Besar Penelitian dan Pengembangan Tanaman Obat dan Obat Tradisional (B2P2TOOT), Badan Penelitian dan Pengembangan Kesehatan (Badan Litbangkes) telah melakukan Riset Tanaman Obat dan Jamu (Ristoja) dengan mengumpulkan 30 jenis tanaman obat. Physalis minima L. (ciplukan) merupakan salah satu tanaman hasil Ristoja yang telah diteliti di Laboratorium Farmasi, Pusat Penelitian dan Pengembangan Biomedis dan Teknologi Dasar Kesehatan, Badan Litbangkes. Penelitian bertujuan mengetahui profil kromatogram tanaman untuk mendapatkan kualitas mutu tanaman dan klaster antara tanaman dari asal geografis yang berbeda menggunakan aplikasi kemometrik. Sampel ciplukan yang terkumpul berjumlah 66 buah dari 15 etnis pada 9 provinsi di Indonesia. Analisis dilakukan menggunakan High Performance Liquid Chromatography (HPLC) dengan detektor Photo Diode Array (PDA) pada panjang gelombang (λ) 254 nm dan 366 nm. Dari hasil optimasi, eluen HPLC yang digunakan adalah campuran asetonitril dan metanol dengan sistem gradien. Hasil dari HPLC diolah secara kemometrik dengan interpretasi data menggunakan Principal Component Analysis (PCA). Hasil PCA dengan HPLC pada λ 254 nm and 366 nm, masing-masing memiliki 2 klaster yang menunjukkan bahwa Physalis minima L. hasil Ristoja memiliki 2 profil fitokimia. Puncak yang terdeteksi pada λ 366 nm lebih kompleks dibanding λ 254 nm.
Article
Full-text available
Physalis alkekengi L. is the only representative of the genus Physalis (Solanaceae) that is native to Bulgaria, found in wild habitats under different climatic and soil conditions. The plant is poisonous, but produces edible fruit, which are a source of functional nutrients—vitamins, phenolic antioxidants, minerals, etc. Therefore, the objective of this work was to determine the presence of certain nutrient and bioactive substances in two phenotypes of P. alkekengi fruit from Bulgaria, in order to better reveal the prospects of fruit use in nutrition. Different macro and micronutrients were determined in the fruit—protein, ash, lipids, fiber, natural pigments, sugars, amino acids, minerals—and the results showed differences between the phenotypes. Fruit energy values were low and identical in the samples, 43 kcal/100 g. The fruits were rich in extractable phenolics (TPC, 17.74–20.25 mg GAE/100 g FW; flavonoids, 15.84–18.03 mg QE/100 g FW) and demonstrated good antioxidant activity (DPPH, 171.55–221.26 mM TE/g; FRAP, 193.18–256.35 mM TE/g). P. alkekengi fruits were processed to obtain a dry extract with ethanol (yield 47.92–58.6%), and its individual composition was identified (GC-MS). The results in this study supported the presumed phytonutritive potential of P. alkekengi fruit, thus, opening doors for further research.
Article
Full-text available
In husk tomato, Physalis ixocarpa Brot., a wide range of self-incompatibility phenotypes was observed upon self-pollination. Self-incompatibility seems to be a polygenic trait of low heritability, affected by inbreeding depression and by environment. Organ coloration and leaf serration also were found to be polygenic traits. The chromosomes of this species are characterized by conspicuous heterochromatic knobs which would facilitate identification of each pair. Attempts to hybridize P. ixocarpa with P. floridiana L. and P. peruviana L. were unsuccessful. Propagation by cuttings is readily attainable in P. ixocarpa and might be useful for growing and intercrossing field selections in isolation plots.
Article
Full-text available
Exotic fruits play an important role in nutrition as an excellent base for low calorie and dietetic products. Highly valued for its unique flavor, texture and color, recent research has shown cape gooseberry (Physalis peruviana) to be high in many beneficial compounds. The diversity of functional applications to which P. peruviana can be put gives this fruit great importance. The food industry has used cape gooseberry in different products including beverages, yogurts and jams. With the rapidly growing popularity of this unique fruit it is important to have a comprehensive reference for its nutritional benefits. This review provides a valuable source for current knowledge on bioactive phytochemicals and further development of P. peruviana for functional foods as well as nutraceutical and pharmaceutical industries.