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Recent advances in pharmacological potential of Syzygium cumini: A review

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Abstract

Syzygium cumini (Linn.) Skeels. (Myrtaceae) (Synonym. Eugenia jambolana), commonly known as Jamun or Black Plum is indigenous to India. The plant has traditionally been used for its rich nutrition and medicinal value. The current review focuses on the recent research investigations involving the studies on diverse pharmacological actions of Jamun. The electronic database search was performed in order to achieve this aim. Jamun plant has been reported to be enriched with an array of phytoconstituents like ellagic acid, glucoside, anthocyanins, kaempferol, isoquercetin, myrecetin and so on. The seeds which are mostly utilized for their medicinal value are said to contain an alkaloid-jambosine and glycoside-jambolin or antimellin which inhibit the conversion of starch to sugar. Different plant parts have been claimed to contain different constituents, due to which they possess an assorted pharmacological prospective. Jamun has been used for the treatment of diabetes since ages. Apart from this it has also shown its beneficial potential as anti-allergic, antibacterial, anticancer, anticlastogenic, anti-diarrhoeal, anti-fertility, anti-fungal, anti-hyperlipidemic, anti-hypertensive, anti-inflammatory, anti-lieshmanial, anti-nociceptive, anti-oxidant, anti-viral, ascaricidal, cardioprotective, chemoprotective, diuretic, gastroprotective, hepatoprotective, hypothermic, neuropsychopharmacological and radioprotective agent. These actions and the lacunas in the specific areas have been discussed in this article. This will provide a platform for the future researchers especially in the less explored areas.
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Advances in Applied Science Research, 2016, 7(3):1-12
ISSN: 0976-8610
CODEN (USA): AASRFC
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Recent advances in pharmacological potential of Syzygium cumini:
A review
Deepti Katiyar
1*
, Vijender Singh
2
and Mohd. Ali
3
1
Department of Pharmacognosy, KIET School of Pharmacy, Ghaziabad, UP, India
2
Department of Pharmacognosy, BBS Institute of Pharmacy, Greater Noida, UP, India
3
Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Jamia Hamdard,
New Delhi, India
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ABSTRACT
Syzygium cumini (Linn.) Skeels. (Myrtaceae) (Synonym. Eugenia jambolana), commonly known
as Jamun or Black Plum is indigenous to India. The plant has traditionally been used for its rich
nutrition and medicinal value. The current review focuses on the recent research investigations
involving the studies on diverse pharmacological actions of Jamun. The electronic database
search was performed in order to achieve this aim. Jamun plant has been reported to be
enriched with an array of phytoconstituents like ellagic acid, glucoside, anthocyanins,
kaempferol, isoquercetin, myrecetin and so on. The seeds which are mostly utilized for their
medicinal value are said to contain an alkaloid- jambosine and glycoside-jambolin or antimellin
which inhibit the conversion of starch to sugar. Different plant parts have been claimed to
contain different constituents, due to which they possess an assorted pharmacological
prospective. Jamun has been used for the treatment of diabetes since ages. Apart from this it has
also shown its beneficial potential as anti-allergic, antibacterial, anticancer, anticlastogenic,
anti-diarrhoeal, anti-fertility, anti-fungal, anti-hyperlipidemic, anti-hypertensive, anti-
inflammatory, anti-lieshmanial, anti-nociceptive, anti-oxidant, anti-viral, ascaricidal,
cardioprotective, chemoprotective, diuretic, gastroprotective, hepatoprotective, hypothermic,
neuropsychopharmacological and radioprotective agent. These actions and the lacunas in the
specific areas have been discussed in this article. This will provide a platform for the future
researchers especially in the less explored areas.
Keywords: Syzygium cumini, Pharmacological activity, Anti-diabetic
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INTRODUCTION
Syzygium cumini (S. cumini) (L.) Skeels (family: Myrtaceae), synonyms- Syzygium jambolana
DC., Eugenia cumini (Linn.) Druce., Syzygium jambolanum (Lam.) DC., Myrtus cumini Linn.,
Eugenia djouant Perr., Eugenia caryophyllifolia Lam., Calyptranthes jambolana Willd.,
commonly known as Black Plum in English, Jamun in Hindi, Jambu in Sanskrit and Jaman in
Urdu is a large evergreen tree indigenous to India, though Syzygium cumini (SC) trees are found
throughout the Asian subcontinent, South America, Eastern Africa, Madagascar and so on [1].
Different plant parts have been reported to contain a variety of components. The fruit pulp
contains Vitamin A & C, nicotinic acid, riboflavin, folic acid, maleic acid, choline, sugar, amino
acid, K, Ca, Na, P, Fe, Mn, Zn. Gallic acid is said to be responsible for the sourness of the fruit
while anthocyanins for the colour. The leaves are enriched with acylated flavonol glycosides,
myricetin, myricitin, quercetin, galloyl carboxylase, esterase and tannins. The flowers are rich in
quercetin, kaempferol, myricetin, oleanolic acid, quercetin-3-D-galactoside, eugenol-triterpenoid
A & B. The roots contain flavonoid glycosides and isorhamnetin 3-O-rutinoside. The stem bark
has betulinic acid, β-sitosterol, quercetin, kaempferol, ellagic acid, gallic acid, myrecetin etc. The
seeds contain glycoside jambolin, gallic acid, essential oils and so on [2]. The various parts of
the tree have been used traditionally for the treatment of various human ailments. SC find its
place in numerous traditional systems of medicine like Ayurveda, Siddha, Unani and
Homeopathic systems of medicine. It was one of the best remedy for diabetes before the
discovery of insulin [3]. As per Ayurveda, the barks of SC possess astringent, acrid, digestive
and wound healing properties. They are beneficial for the treatment of biliousness, dysentery,
sore throat, bronchitis, thirst, asthma and ulcers. According to Siddha system of medicine, it
supposed to be semen promoting, haematinic and hypothermic. Unani System of medicine
characterizes it to be a tonic for liver, to enrich blood, reinforce teeth and gums [4].
PHARMACOLOGICAL ACTIONS OF SYZYGIUM CUMINI
1.Anti-allergic
Allergy is an abnormal reaction of the body to the allergen introduced by ingestion, injection,
inhalation or skin contact. A novel, safe and effective remedy is required for this ailment. In an
investigation, the aqueous extract of SC leaves (25-100mg/kg, p.o.) inhibited the rat paw edema
induced by 48/80 (allergenic compound), histamine and 5-HT. However, the extract could not
produce any beneficial effects against the platelet aggregating factor-induced paw edema [5].
2.Antibacterial
Now a days, people have started using antibiotics as OTC (Over The Counter) drugs which has
led to antibiotic resistance, thus safer novel antibacterial agents are required. In case of SC, its
stem, leaf and fruit extracts were found to be effective against all the bacterial strains used in the
study. Best results were observed against Roultella plantikola (zone of inhibition-25 mm) [6].
Microbroth dilution and Agar well diffusion assays were utilized to study the antibacterial effects
of SC seeds against multidrug-resistant human bacterial pathogens and it was found that the ethyl
acetate fraction from the ethanol extract was most effective. Then, the ethyl acetate fraction was
subjected to phytochemical analysis and TLC-bioautography which exhibited the phenolics to be
the main component responsible for the activity [7].
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Ethyl acetate, petroleum ether and methanolic extracts of the SC leaf were found to be effective
against Salmonella typhimurium, Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus
aureus and Enterobacter aerogenes [8].
Acetone, aqueous and ethanolic bark extracts were evaluated for their antibacterial effects
against twelve strains of Vibrio cholera, of which the ethanolic extract was found to be most
effective [9].
Aqueous leaf extract of SC has shown beneficial effects against Klebsiella sp., Salmonella
paratyphi A & B, Citrobacter sp., Proteus mirabilis, Escherichia coli, Staphylococcus aureus,
Shigella sonnei, Pseudomonas aeruginosa, Salmonella typhimurium, Shigella boydii,
Streptococcus faecalis, Shigella flexneri and Salmonella typhi [10].
3.Anti-cancer
Various treatment strategies for cancer involve surgery, hormonal therapy, chemotherapy,
radiation therapy and targeted therapy (e.g. monoclonal antibody therapy and immunotherapy).
Apart from killing cancerous cells, some normal, healthy cells may be destroyed and may affect
many vital organs such as kidney, heart, lungs, nervous system etc. Many herbal anti-cancer
drugs are being used to avoid the unwanted side effects.
Ellagitannins isolated from SC have shown to inhibit Wnt signaling in a transfected human 293T
cell line [11].
A few of the current investigations have proved the selective cytotoxic activity of jamun fruit
extract after studying its pro-apoptotic and antiproliferative effects on estrogen independent
(MDA-MB-231) breast cancer cells, estrogen dependent/aromatase positive (MCF-7aro)and
normal/nontumorigenic (MCF-10A) breast cell line [12] [1].
Anti-cancer effects of 40% SC extract have been studied on human cervical cancer cells (11.8%
growth inhibition observed in SiHa (HPV-16 positive) cells and 14.4% in HeLa (HPV-18
positive) cells) [13].
4.Anticlastogenic
Anticlastogenic agent is one which protects the disruption or breakages of chromosomes. SC
extract has exhibited its utility in mutagenesis prevention and carcinogenesis initiation. The
alcoholic seed extract decreased the hydroxyl radical induced strand breaks in pBR322 DNA in
vitro and the aqueous extract was found to reduce the chromosomal aberrations in mice (induced
by DBMA and urethane) [14].
5.Anti-diabetic
Various preclinical and clinical studies have been performed to evaluate the anti-diabetic
potential of SC [15].
Numerous investigations performed in the past have indicated that SC seeds [16] [17] [18] [19]
[20] [21], fruit pulp [22] [23] [24], whole fruit [25] [26], bark [27] [28], leaves [29] and flowers
[30] possess anti-diabetic activity.
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Mycaminose (50 mg/kg) - a compound isolated form SC seeds and ethyl acetate & methanol
fraction at the doses of 200 and 400 mg/kg showed a significant (p<0.05) decrease in blood
glucose level when evaluated for the anti-diabetic activity in streptozotocin (STZ)-induced
diabetes in rats [31].
The aqueous and alcoholic SC extracts were evaluated for their anti-diabetic potential in alloxan
induced diabetic rabbits. It was found that the aqueous extract was more effective in improving
blood glucose in glucose tolerance test and in decreasing fasting blood glucose [24].
Numerous studies have been performed to show the beneficial effects of SC extract in
normalizing the elevated lipid profiles of diabetic rats [16] [22] [32], elevating the serum insulin
[16] [32] and increasing SOD and GPx activities [16]. The SC seeds possess protective effect
against diabetes related complications like neuropathy [33], gastropathy [33], nephropathy [33],
diabetic cataract [34] and also reduced peptic ulceration [35].
SC possesses the potential to inhibit the carbohydrate hydrolyzing enzymes [36]. A polyherbal
formulation (ADJ6) containing SC and some other antidiabetic herbs have shown a significant
inhibitory action against α-glucosidase and α-amylase [37]. SC seeds have shown the pancreatic
islet cells regeneration potential in streptozotocin [38] and alloxan [39] diabetic rats.
Various clinical studies have been performed to validate the use of SC in diabetes [40] [26]. In a
recent open labeled randomized parallel designed controlled study, Type II diabetic individuals
were administered the standardized SC seed powder which exhibited a reduction in fasting blood
sugar, insulin resistance and elevation in HDL cholesterol at the end of 3rd month [41].
6.Anti-diarrheal
Natural products are a drug of choice for diseases like diarrhea. SC ethanolic extract (400 mg/kg)
administered orally has exhibited a reduction in gastrointestinal activity in PGE2 induced
enteropooling and castor oil induced diarrhea in rats [42].
7.Anti-fertility
A review has stated that oleanolic acid – a phytoconstituent isolated from the flowers of SC has
the potential to arrest spermatogenesis, thus exhibiting the anti-fertility action in the male albino
rats [4].
8.Antifungal
The indiscriminate utilization of medicines has led to resistance against some fungal species,
thus there is a requirement of a safer remedy.
The methanolic fruit extract of SC has shown excellent antifungal action against the targeted
pathogenic fungi - Fusarium oxysporium, Rhizoctonia solani and Sclerotium rolfsii [43].
A research investigation utilized different concentrations of n-hexane, alcohol and aqueous
extracts of different plant parts of SC (barks of stem and roots, fruits and leaves) to study their
antifungal potential against Ascochyta rabiei-the causative agent for blight disease of Cicer
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arietinum. All the aqueous extracts, n-hexane extract of stem-bark and alcoholic extracts of both
the barks exhibited significant antifungal activity [44].
The aqueous, benzene, chloroform, ethanol, methanol and petroleum ether extracts of SC leaf
were evaluated against various species of Aspergillus i.e., A. tamari, A. niger, A. ochraceus, A.
flavus, A. columnaris, A. fumigates, A. candidus and A. flavipes. The results revealed that the
methanolic extract was most potent [10].
9.Anti-hyperlipidemic
Of the various lipid-lowering drugs available in the market, the herbal drugs are found to be
more safe and efficacious. The anti-hyperlipidemic potential of SC fruit pulp was evaluated in
diet induced hyperlipidaemic rats. The results revealed that the fruit pulp was as potent as
simvastatin in reducing serum LDL cholesterol, triglycerides & total cholesterol and elevating
HDL cholesterol [45].
Flavonoids isolated from the seeds have exhibited hypolipidemic effects in diabetic rats [21]
[20].
The ethanoilc extract of SC kernels (100 mg/kg b.w.) was evaluated for its hypolipidemic
potential for the levels of triglycerides, cholesterol, phospholipids, free fatty acids in the plasma,
kidney and liver tissues of STZ (55 mg/kg b.w.) induced diabetic rats. The results showed that
the extract was able to restore all the parameters to their normal range [46].
10. Anti-inflammatory
The anti-inflammatory drugs are those which help to overcome a localized physical condition in
which part of the body becomes reddened, swollen, hot, and often painful, especially as a
reaction to injury or infection.
Ethyl-acetate and methanolic extracts of SC leaves and seeds (both at the doses of 200 and 400
mg/kg p.o.) showed a significant anti-inflammatory activity in carrageenan induced paw oedema
in wistar rats [47] [48].
11. Antilieshmanial
Antilieshmanial agents are those that destroy protozoa of the genus Leishmania. The essential oil
of SC and its main component α-pinene was evaluated for its antilieshmanial action against
Leishmania amazonensis. α-pinene showed its efficacy with IC50 of 19.7 mg/ml.
Immunomodulatory action was considered as the most probable mechanism of action [49].
12. Antinociceptive
Antinociceptive activity is a process of blocking the detection of a painful or injurious stimulus
by sensory neurons. With SC, the hydro-alcoholic leaf extract was evaluated for its analgesic
potential in rats. To assess the cutaneous nociception, hot plate and formalin tests were used
while for muscular nociception, forelimb grip force was measured. The extract at the dose of
100–300 mg/kg i.p. exhibited a significant decrease in the pain scores in all the phases of the
formalin test but extract even at the dose of 300 mg/kg was not able to modify the grip force in
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intact rats. Therefore, the extract exhibited an excellent analgesic activity (on cutaneous and deep
muscle pain) [50].
The methanolic extract of SC fruits exhibited a significant central analgesic activity which was
investigated using the Eddy’s Hot Plate method [43].
13. Antioxidant
Generation of free radicals initiates/aggravates various diseases like cancer, AIDS, arthiritis,
Alzheimer and diabetic complications. Thus, there is a requirement of safer drugs that have
property of scavenging the free radicals.
With regard to SC fruit, polyphenols have shown outstanding antioxidant capacity when
compared to the standard polyphenols [51].
The methanolic extract of leaves, bark and seeds of SC were fractionated in different solvents: n-
hexane, chloroform, ethyl acetate, butanol and water. These fractions were studied for their
antioxidant and free radical scavenging activities. Of all the fractions, the polar ones i.e., ethyl
acetate and water fractions showed excellent results [52].
The leaf and seed extract of SC exhibited a significant antioxidant activity when they were
assessed by various in vitro methods such as Ferric reducing antioxidant power (FRAP) assay,
2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging assay, Nitric oxide radical scavenging, ABTS
Assay, Total Reducing antioxidant potential, Total antioxidant activity, Reducing power and
Hydroxyl radical scavenging activity[53].
RSC (Radical Scavenger Capacity) of SC was determined by using DPPH (2, 2-diphenyl-1-
picrylhydrazyl radical) assay. The second order rate constants-k2 was evaluated to determine
RSC and then these were compared to natural and synthetic antioxidants. The k2 value of SC
was determined to be 15.60 L/mol g s in methanol at 25°C proving that it has a excellent anti-
oxidant potential [54].
14. Antiviral
With the changing environment, new viral diseases are being identified, so there is a demand for
a safer, non-toxic remedy. The cold and hot aqueous extracts of leaves and barks of SC were
evaluated for their antiviral potential against H5N1 (avian influenza virus which causes a highly
contagious disease of poultry) using CPE reduction assay to establish virucidal, pre-exposure and
post-exposure potential of these extracts. With hot and cold aqueous bark extracts and hot
aqueous leaf extracts, 100% inhibition of the virus was observed in virus yield reduction assay
and in egg based in ovo assay. CC50/EC50 (selective index) for cold aqueous extract (43.5) and
hot aqueous extract (248) of bark exhibited their potency against H5N1 virus [55]. The aqueous
extract of leaves was also found to inhibit the goatpox virus [56] and the buffalopox virus [57].
15. Ascaricidal
Different SC extracts were used to study their ascaricidal action against Tetranychus urticae
Koch. The results showed the inhibition rate of 98.5%, 94% and 90% respectively for ethanolic,
hexane and ethyl acetate extracts [58].
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16. Cardioprotective
In case of SC, the hydroalcoholic extract of leaves was evaluated in spontaneously hypertensive
and normotensive wistar rats. The findings of the research investigation revealed that the extract
decreased the blood pressure as well as the heart rate. Extracellular calcium influx and inhibition
of arterial tone were suggested as the most probable mechanism of action [59]. The
hydroalcoholic extract of SC was evaluated for its antihypertensive, and vasorelaxant effect.
Polyethylene catheters were inserted into the inferior vena cava and lower abdominal aorta in the
anaesthetized rats for dosing and measuring blood pressure. The extract at the doses of 0.5; 1; 5;
10; 20 and 30 mg/kg, i.v. was able to induce hypotension (due to reduction in endothelium
mediated peripheral resistance) and bradycardia (due to meandering cardiac muscarinic
activation) [60].
The elevated serum levels of alanine transaminase (ALT), serum creatine phosphokinase (CPK),
aspartate transaminase (AST), lactate dehydrogenase (LDH), HDL-cholesterol due to
Doxorubicin(1.5 mg / kg/b.w., 15 days) induced cardiotoxicity were brought to normal range
after the administration of aqueous suspension of SC seed extract (100 mg/kg/b.w. for 15 days)
[61].
The oral administration of the methanolic extract of SC at the doses of 250 mg/kg and 500 mg/kg
consecutively for 30 days reversed and retained the activity of AST, ALT, LDH and CPK to
normal levels against the isoproterenol- induced myocardial infarction [62].
17. Chemoprotective
Various herbal drugs have proved their beneficial effect in protecting healthy tissues from the
toxic effects of anti-cancer drugs. The aqueous and ethanolic SC seed extracts have shown
chemoprotective action in the in vivo oxidative stress and genomic damage [63].
It has been reported that SC extract in the doses of 125 and 250 mg/kg/b.w./animal/day exhibited
the cancer chemopreventive properties in the DMBA-induced croton oil promoted two stage skin
carcinogenesis in Swiss albino mice. It was found that the extract was able to decline the tumor
incidence, cumulative number of papillomas and elevate the average latency time as compared to
the control group [64] [65].
The tumor burden, tumor incidence and cumulative number of gastric carcinomas induced by
benzo-a-pyrene were found to decrease after the treatment with 25 mg/kg b.w./day of the SC
extract exhibiting its broad spectrum chemoprotective effects [66].
The genotoxic effects caused by of the carcinogens urethane and DMBA in mice were also found
to decline after the administration of SC seed extract [14].
18. Diuretic
The Diuretics are used for the treatment of various human ailments such as heart failure, high
blood pressure, liver disease, some types of kidney disease and also in cases overdose or
poisoning. Now day’s herbs are a better option as diuretics.
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Petroleum ether, chloroform, methanolic and aqueous extracts of SC bark were evaluated for
their diuretic activity in Wistar albino rats at the dose of 500mg/kg body weight. The methanolic
and aqueous extracts were found to be active as diuretic as depicted by an elevation in total urine
output and in the excretion of electrolyte concentration of sodium and potassium ions [67].
19. Gastroprotective
Natural products provide a safer remedy to protect the gastric mucosa of aggressive or irritating
agents.
Seed kernel extract of SC (200 mg/kg) was evaluated for its antiulcer activity. First, the diabetes
was induced using low dose streptozotocin (35mg/kg) in combination with high fat diet. Then,
the gastric ulceration was produced in diabetic rat’s ethanol and indomethacin models. It was
observed that there was a significant decrease in the gastric ulcer index after the administration
SC extract alone and as well as in combination with Acarbose (5mg/kg) [68].
In another research investigation, the hard liquor (48% ethanol- 1ml/150gm b.w.) and aspirin
(200 mg/kg, orally) were used to induce gastric ulcer in rats. The aqueous extract of SC leaves at
the doses of 200 and 400 mg/kg produced ulcer inhibition (%) of 32.17% and 61.09%
respectively in hard liquor model and 23.01% and 70.33% respectively in aspirin model [69].
SC fruit extract at the dose of 200mg/kg b.w. was administered orally for 10 days to
streptozotocin induced diabetic and to rats exposed to ulcerogens (like aspirin, 95% ethanol,
cold-resistant stress and pylorus-ligation). The observations of the study revealed that there was
a decrease in acid-pepsin secretion, cell shedding and LPO while an increase in the GSH (in
gastric mucosa), mucosal glycoprotein and mucin [35] [70] [71].
20. Hepatoprotective
Hepatoprotective agents are those that provide protection to the liver (which performs important
functions like metabolism, secretion, storage, and detoxification of endogenous and exogenous
substances).
The alcoholic extract of the pulp of SC (100 and 200mg/kg/day) exhibited a significant
hepatoprotective action on paracetamol (PCM)-induced hepatotoxicity in albino rats. The
elevated serum levels of ALT, AST, AP were decreased and histopathological studies depicted a
reduction in fibrosis and necrosis [72].
The anthocyanins rich SC pulp extract (50 to 500 ppm) has shown its beneficial effects in
preventing the CCl
4
induced liver damage by declining the lipid peroxidation, suppressing the
CCl
4
-induced release of LDH, and elevating the GPx (antioxidant enzyme) activity [73].
Aqueous leaf extract [74] and methanolic seed extract [75] have also shown hepatoprtective
effects through biochemical estimations and histopathological studies.
21. Hypothermic
In an research investigation, after insertion of a mister probe into the rectum of rats , the basal
body temperature was recorded and then pyrexia was induced by Brewer’s yeast (Sacchromyces
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cerevisiae)( 10mL/kg of 20% suspension, subcutaneous). After 18 hours, the rectal temperature
of the rats was again recorded and the test group was treated with SC methanolic fruit extract
(100 mg/kg, orally). The standard group was administered oral dose of 33mg/kg of paracetamol
and control group was given 0.2 ml normal saline. Upto 3 hours, temperature was recorded
hourly and % reduction in temperature was recorded. The extract exhibited a significant
antipyretic activity as compared to standard [43]. The chloroform and methanolic extracts of SC
have also shown antipyretic activity [76].
22. Inhibits lipid peroxidation
Some enzymatic and non-enzymatic reactions lead to lipid peroxidation associated with
mutagenesis and cellular damage. The fruit pulp, seed coat and kernel extracts were evaluated for
their lipid peroxidation inhibition activity and was seen that the seed and coat and the pulp
extracts were less active than the kernel [77].
An research investigation utilized the pulp extract (enriched with anthocyanins) to study its
potential to inhibit the iron (FeSO4)-induced lipid peroxidation in different organs of rat (Liver,
liver mitochondria, brain, testes etc.) in vitro. A concentration of 5ppm was found to show
beneficial results with highest lipid peroxidation inhibition in liver mitochondria (86%), followed
by liver (83%), testes(72%) and brain(68.3%) [78].
SC seed extract when administered orally for 15 days to alloxan treated rats, exhibited an
elevated antioxidant the enzyme level and declined lipid peroxidation activity [79].
23. Neuropsychopharmacological
Neuropsychopharmacological agents include the studies of anxiety disorders, affective
disorders, psychotic disorders, degenerative disorders, eating behavior, and sleep behavior. The
methanolic SC extract has exhibited the antiamnesic activity against scopolamine induced spatial
impairments in rats [80]. The methanolic and ethyl acetate SC seed extracts at the doses of 200
mg/kg and 400 mg/kg were evaluated for their CNS activity utilizing rota rod and
actophotometer. A significant CNS activity was observed for both the extracts [81].
24. Radioprotective
Radioprotective agents are those that reduce the effect of radiation on tissues. SC leaf extract
provided protection against radiation induced intestinal mucosal damage due to exposure of
different doses of gamma radiations [82].
Dichloromethane extract of SC leaf and Hydroalcoholic seed extract when administered
intraperitoneally exhibited radioprotective effects [83] [84]. SC leaf extract in various
concentrations (0.0, 1.56, 3.125, 6.25, 12.5, 25, 50 and 100 µg/ml) was found to reduce the
radiation induced DNA damage in the cultured human peripheral blood lymphocytes [85].
CONCLUSION
The present article has focused on the recent research investigations carried out on the diverse
pharmacological actions of Jamun. Various parts of the plant and their extracts have been used
for anti-diabetic action, but very less study has been performed on its isolated phytoconstituents
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and very few clinical trials have been carried out. Apart from its utility in diabetes, it is a very
useful drug as anti-bacterial, anti-fungal, anti-viral, anti-cancer, anti-hyperlipidemic,
hepatoprotective, cardioprotective, gastroprotective and so on. Its potential as anti-fertility agent
needs to be explored in order to establish its safety on long term use. Thus, further studies need
to be performed with respect to pharmacological action of its isolated constituents, its
mechanism of action and clinical studies.
Acknowledgements
The authors are thankful to the Principal, KIET School of Pharmacy for motivation. Authors are
also thankful to KIET LIBRARY and NISCAIR, New Delhi for providing the literature.
Conflicts of interest
There are no conflicts of interest.
REFERENCES
[1] Li L, Zhang Y, Seeram NP, Nat. Prod. Commun., 2009, 4, 217219
[2] Ayyanar M, Subash-Babu P, Asia. Pac. J. of Trop. Biomed., 2012, 240-246.
[3] Helmstadter A, Die Pharmazie, 2007, 62, 717720.
[4] Balinga MS, Bhat HP, Balinga BRV, Wilson R, Palatty PL, Food Res. Int., 2011, 1-14.
[5] Brito FA, Lima LA, Ramos MF, Nakamura MJ, Cavalher-Machado SC, Siani AC, Braz. J
Med. Biol. Res., 2007, 40, 105−115.
[6] Pareek A, Meena RK, Yadav B, Ind. J. Appl. Res., 2015, 5(9), 64-66.
[7] Bag A, Bhattacharyya SK, Pal NK, Chattopadhyay RR, Microb. Res., 2012, 167, 352– 357.
[8] Kaneria M, Baravalia Y, Vaghasiya Y, Chanda S, Ind. J. Pharm. Sci., 2009, 71, 406−412.
[9] Sharma A, Patel VK, Chaturvedi AN, Ind. J. Pharmacol., 2009, 41, 129−133.
[10] Satish S, Raghavendra MP, Raveesha KA, Adv. in Biol. Res., 2008, 2, 44−48.
[11] Sharma M, Li L, Celver J, Killian C, Kovoor A, Seeram NP, J. Agri. Food Chem., 2010,
58, 3965−3969.
[12] Li L, Adams LS, Chen S, Killian C, Ahmed A, Seeram NP, J. Agri. Food Chem., 2009, 57,
826−831.
[13] Barh D, Viswanathan G, E canc. med. sci., 2008, 2, 83.
[14] Arun R, Prakash MV, Abraham SK, Premkumar K, J. Ethnopharmacol., 2010, [Epub
ahead of print].
[15] Helmstädter A, Die Pharmazie, 2008, 63, 91−101.
[16] Sharafeldin K, Rizvi MR, J. Bas. Appl. Zool., 2015, 72, 126–134.
[17] Sikder MAA, Kaisar MA, Rahman MS, Bang. Pharm. J., 2011, 14(2), 87-91.
[18] Panda DK, Ghosh D, Bhat B, Talwar SK, Jaggi M, Mukherjee R., Meth. Find. Exper. Clin.
Pharmacol., 2009, 31, 571−584.
[19] Mastan SK, Latha TB, Latha TS, Srikanth A, Chaitanya G, Kumar KE, Ph OL, 2009, 3,
845-850.
[20] Sharma B, Balomajumder C, Roy P, Food Chem. Toxicol., 2008, 46, 2376−2383.
[21] Sharma B, Viswanath G, Salunke R, Roy P, Food Chem., 2008, 110, 697−705.
[22] Srivastava B, Sinha AK, Gaur S, Barshiliya Y, Asia. J. Pharm. Life Sci., 2012, 2(1), 10-19.
[23] Sundaram EN, Reddy PU, Singh KP, Ind. J. Pharm. Sci., 2009,71, 594−598.
[24] Sharma SB, Nasir A, Prabhu KM, Murthy PS, J. Ethnopharmacol., 2006, 104, 367-373.
Deepti Katiyar et al Adv. Appl. Sci. Res., 2016, 7(4):1-12
_____________________________________________________________________________
11
Pelagia Research Library
[25] Gupta R, Saxena AM, Asia. J. Pharm. Biol. Res., 2011, 267-272.
[26] Safdar M, Khan A, Habibullah, Pak J Nutri., 2006, 5(6), 573-576.
[27] Saravanan G, Pari L, J. Pharmacol. Toxicol., 2008, 3(1), 1-10.
[28] Villasenor IM, Lamadrid MR, J. Ethnopharmacol., 2006, 104, 129−131.
[29] Sreevani D, Devaraju T, Sekhar PR, Savitri Y, Nagalakshamamma K, Yashodamma N, The
Ecoscan, 2011, 1, 93-97.
[30] Tehzeeb-ul-Nisa Qadir MI, Malik SA, Ph OL, 2010, 2, 979-985.
[31] Kumar A, Ilavarasan R, Jayachandran T, Deecaraman M, Aravindan P, Padmanabhan N,
Krishan MRV, J. Med. Pl. Res., 2008, 2(9), 246-249.
[32] Jasmine R, Daisy P, Asia. J. Biochem., 2007, 2(4), 269-273.
[33] Grover JK, Rathi SS, Vats V, Ind. J. Exp. Biol., 2002, 40, 273−276.
[34] Rathi SS, Grover JK, Vikrant V, Biswas NR, Phytother. Res., 2002, 16, 774−777.
[35] Chaturvedi A, Bhawani G, Agarwal PK, Goel S, Singh A, Goel RK, Ind. J. Physiol. &
Pharmacol., 2009, 53, 137−146.
[36] Singh A, Marar T, J. Cell Tiss. Res., 2011, 11(1), 2535-2539.
[37] Duraiswamy A, Shanmugasundaram D, Sasikumar CS, Cherian SM, Cherian KM, J. Trad.
& Complement. Med., 2015, 1-5.
[38] Dusane MB, Joshi BN, J. Chin. Integr. Med., 2011, 9(12), 1380-1387.
[39] Singh N, Gupta M, Ind. J. Exp. Biol., 2007, 45, 861-867.
[40] Waheed A, Miana GA, Ahmad SI, Pak. J. Pharmacol, 2007, 24(1), 13-17.
[41] Sahana DA, Shivaprakash G, Baliga R, Adhikari PMR, Jyothi G, Pai MRSM, J. Pharm.
Res., 2010, 3, 1268−1270.
[42] Mukherjee P, Saha K, Murugeresan T, Mandal SC, Pal M, Saha BP, India. J.
Ethnopharmacol., 2011, 60, 85-89.
[43] Pant OP, Chandra M, Sethi S, Punetha H, Dixit S, Pant AK, Ind. J. Pharm. Biol. Res.,
2014, 2(1), 26-34.
[44] Jabeen K, Javaid A, Nat. Prod. Res., 2010, 24(12), 1158-67.
[45] Rabiea B, Manzar Z, Ahmad U, Shahnaz A, Azam Z, J. Pak. Med. Assoc., 2011, 61(5),
433-437.
[46] Kasiappan R, Subbaih R, Sorimuthu S, Food Chem. Toxicol., 2005, 43, 1433–1439.
[47] Jain A, Sharma S, Goyal M, Dubey S, Jain S, Sahu J, Sharma A, Kaushik A, Int. J.
Phytomed., 2010, 2, 124-126
[48] Kumar A, Ilavarasan R, Jayachandran T, Deecaraman M, Mohan Kumar R, Aravindan P, J.
Biotechnol., 2008, 7, 941−943.
[49] Klinger AFR, Layane VA, Clarice ND, Denise FCM, Sabrina MPC, Fernando AAC, J.
Ethnopharmacol., 2015, 160, 32–40.
[50] Avila-Pena D, Pena N, Quintero L, Suarez-Roca H, J. Ethnopharmacol., 2007, 112(2),
380-385.
[51] Singh JP, Kaur A, Singh N, Nim L, Shevkani K, Kaur H, Arora DS, LWT - Food Sci.
Technol., 2016, 65, 1025-1030.
[52] Haroon R, Jelani S, Arshad FK, Int. J. Res.- Granthaalayah, 2015, 3(5), 13-26.
[53] Nair LK, Begum M, Geetha S, JESTFT, 2013, 7(1), 54-62.
[54] Rufino MSM, Alves RE, Fernandes FAN, Brito ES, Food Res. Int., 2011, 44, 2072–2075.
[55] Sood R, Swarup D, Bhatia D, Kulkarni DD, Dey S, Saini M, Dubey SC, Ind. J. Exp. Biol.,
2012, 50, 179-18.
Deepti Katiyar et al Adv. Appl. Sci. Res., 2016, 7(4):1-12
_____________________________________________________________________________
12
Pelagia Research Library
[56] Bhanuprakash V, Hosamani M, Balamurugan V, Gandhale P, Naresh R, Swarup D, Ind. J.
Exp. Biol., 2008, 46, 120−127.
[57] Bhanuprakash V, Hosamani M, Balamurugan V, Singh RK, Swarup D, Int. J. Trop. Med.,
2007, 2, 3−9.
[58] Afify AEMMR, Beltagi HSE, Fayed SA, Shalaby EA, Asia. Pac. J. Trop. Biomed., 2011,
359-364.
[59] Rachel MR, Vicente FPN, Kllysmann SR, Denilson AV, Iracelle CA, Selma do
Nascimento S, Evi. Complement. Altern. Med., 2014, 1-7.
[60] Herculano EDA, Costa CDF, Rodrigues AKBF, Junior JXA, Santana AEG, França PHB, et
al., Trop. J. Pharm. Res., 2014, 13(11), 1853-1861.
[61] Patel S, Shanmugarajan TS, Somasundaram I, Maity N, Int. J. Phar. Life Sci., 2010, 1(6),
343-349.
[62] Mastan SK, Chaitanya G, Bhavya Latha T, Srikanth A, Sumalatha G, Eswar Kumar K,.
Der Pharmacia Lettre, 2009, 143−149.
[63] Renganathan AM, Velayutham DP, Suresh KA, Kumpati P, J. Ethnopharmacol., 2011,
134(2), 329-333.
[64] Parmar J, Sharma P, Verma P, Goyal PK, Asia. Pac. J. Can. Prev., 2010, 11, 261−265.
[65] Parmar J, Sharma P, Verma P, Sharma P, Goyal PK, Integrat. Can.Thera., 2010, [Epub
ahead of print].
[66] Goyal PK, Verma P, Sharma P, Parmar J, Agarwal A, Asia. Paci. J. Can. Prev., 2010, 11,
753−758.
[67] Chandravarkar S, Mamle Desai SN, Int. J. Res. Ayurveda. Pharm., 2014, 5(1), 102-104.
[68] Jonnalagadda A, Maharaja KK, Kumar P, J. Diab. Metab., 2013, 4(1), 1-6.
[69] Bhargava S, Bhargava P, Jain UK, Ph. OL, 2009, 3, 266-274.
[70] Chaturvedi A, Bhawani G, Agarwal PK, Goel S, Singh A, Goel RK, Ind. J. of Physiol. &
Pharmacol., 2009, 53, 16−24.
[71] Chaturvedi A, Kumar MM, Bhawani G, Chaturvedi H, Kumar M, Goel RK, Ind. J. of
Physiol. & Pharmacol., 2007, 51, 131−140.
[72] Das S, Sarma G, J. Clin. & Diag. Res., 2009, 3, 1466-1474.
[73] Veigas JM, Shrivasthava R, Neelwarne B, Toxicol. In Vitro., 2008, 22, 1440−1446.
[74] Moresco RN, Sperotto RL, Bernardi AS, Cardoso RF, Gomes P, Phytother. Res., 2007, 21,
793−795.
[75] Sisodia SS, Bhatnagar M, Ind. J. Pharmacol., 2009, 41, 23−27.
[76] Sehwag S, Das M, Ind. J. Nat. Prod. Res., 2014, 5(4), 295-307.
[77] Benherlal PS, Arumughan C, J. Sci. Food & Agri., 2007, 87, 2560−2569.
[78] Veigas JM, Narayan MS, Laxman PM, Neelwarne B, Food Chem., 2007, 105, 619−627.
[79] Krishnamoorthy P, Vainthinathan S, Bhuvaneswari A, Nat. Prod. Rad., 2006, 5(2), 103-
107.
[80] Alikatt KL, Akondi BR, Yerragunta VG, Veerareddy VG, Veerareddy PR, Palle S, Brain &
Dev., 2012, 34(10), 844-851.
[81] Kumar A, Padmanabhan N, Krishnan MRV, Pak. J. of Nutri., 2007, 6(6): 698-700.
[82] Jagetia GC, Shetty PC, Vidyasagar MS, Ph. OL, 2008, 1, 169−195.
[83] Jagetia GC, Baliga MS, Die. Nahrung., 2003, 47, 181−185.
[84] Jagetia GC, Baliga MS, Venkatesh P, J. Radia. Res., 2005, 46, 59−65.
[85] Jagetia GC, Balinga MS, Toxicol. Let., 2002, 132(1), 19-25.
... Saponins are established antimicrobial agents as they can mediate the leakage of proteins and certain enzymes from invading pathogenic cells [24]. Besides, steroids possess antibacterial attributes as there is a relationship between membrane lipids and their sensitivity to steroidal compounds, which establishes the proposed mechanism of steroids' antibacterial action via their association with membrane lipids to cause leakages from liposomes [25]. Interestingly, some bioactive phytochemicals are bioavailable in S. cumini, M. oleifera, and T. cordifolia plants [25][26][27]. ...
... Besides, steroids possess antibacterial attributes as there is a relationship between membrane lipids and their sensitivity to steroidal compounds, which establishes the proposed mechanism of steroids' antibacterial action via their association with membrane lipids to cause leakages from liposomes [25]. Interestingly, some bioactive phytochemicals are bioavailable in S. cumini, M. oleifera, and T. cordifolia plants [25][26][27]. ...
... Typically, only the aqueous and ethanol extracts of S. cumini showed concentration-dependent effectiveness against all Candida species tested. This observation agrees with earlier reports that documented the antibacterial activities of S. cumini and implicated its high bioactive phytochemical components for its antimicrobial activities [25]. However, the chemical properties of extraction solvents play decisive roles in demonstrating plants' antifungal properties, as the presence of the phytochemicals extracted by the solvents may relate to the diverse antifungal activities against the Candida strains [15]. ...
Article
Full-text available
AbstractIntroductionThe burden of multiple drug resistance in human pathogens has necessitated the search for anddevelopment of antimicrobial agents with a wide range of structural classes and potentials to selectively acton the several mechanisms of actions exhibited by the pathogens. However, most synthetic antimicrobialagents have been linked with adverse side effects and high costs, furthering the need to explore moreoptions. Syzygium cumini, Moringa oleifera, and Tinospora cordifolia are three medicinal plants used intraditional medicine systems for various infectious diseases. They contain various phytochemicals thatexhibit antimicrobial activities against various bacteria, fungi, and parasites. The mechanisms of theirantimicrobial action may involve the disruption of microbial cell walls and membranes, the inhibition ofmicrobial enzyme and biofilm formation, the modulation of microbial gene expression and quorum sensing,and the induction of microbial cell death. Therefore, the present study evaluated the potentials of aqueousand ethanol extracts of S. cumini, M. oleifera, and T. cordifolia in managing infections as measured by theirinhibitory effects on species. (PDF) Antimicrobial and Synergistic Effects of Syzygium cumini, Moringa oleifera, and Tinospora cordifolia Against Different Candida Infections. Available from: https://www.researchgate.net/publication/383127050_Antimicrobial_and_Synergistic_Effects_of_Syzygium_cumini_Moringa_oleifera_and_Tinospora_cordifolia_Against_Different_Candida_Infections [accessed Aug 15 2024].
... SC aqueous leaf extract has been proven to be effective against Klebsiella sp., Salmonella [92]. ...
... RSC was calculated using the second-order rate constants K2, which were then compared to synthetic and natural antioxidants. SC's K2 value in methanol at 25°C was found to be 15.60 L/mol g s, indicating that it has excellent antioxidant potential [92]. ...
... During carrageenan-induced paw edema tests conducted on Wistar rats, it was observed that methanolic and ethyl-acetate extracts derived from Syzygium cumini seeds and leaves, administered orally at dosage of 200 and 400 mg/kg , displayed significant anti-inflammatory effects [92]. ...
... Saponins are established antimicrobial agents as they can mediate the leakage of proteins and certain enzymes from invading pathogenic cells [24]. Besides, steroids possess antibacterial attributes as there is a relationship between membrane lipids and their sensitivity to steroidal compounds, which establishes the proposed mechanism of steroids' antibacterial action via their association with membrane lipids to cause leakages from liposomes [25]. Interestingly, some bioactive phytochemicals are bioavailable in S. cumini, M. oleifera, and T. cordifolia plants [25][26][27]. ...
... Besides, steroids possess antibacterial attributes as there is a relationship between membrane lipids and their sensitivity to steroidal compounds, which establishes the proposed mechanism of steroids' antibacterial action via their association with membrane lipids to cause leakages from liposomes [25]. Interestingly, some bioactive phytochemicals are bioavailable in S. cumini, M. oleifera, and T. cordifolia plants [25][26][27]. ...
... Typically, only the aqueous and ethanol extracts of S. cumini showed concentration-dependent effectiveness against all Candida species tested. This observation agrees with earlier reports that documented the antibacterial activities of S. cumini and implicated its high bioactive phytochemical components for its antimicrobial activities [25]. However, the chemical properties of extraction solvents play decisive roles in demonstrating plants' antifungal properties, as the presence of the phytochemicals extracted by the solvents may relate to the diverse antifungal activities against the Candida strains [15]. ...
Article
Full-text available
The burden of multiple drug resistance in human pathogens has necessitated the search for and development of antimicrobial agents with a wide range of structural classes and potentials to selectively act on the several mechanisms of actions exhibited by the pathogens. However, most synthetic antimicrobial agents have been linked with adverse side effects and high costs, furthering the need to explore more options. Syzygium cumini, Moringa oleifera, and Tinospora cordifolia are three medicinal plants used in traditional medicine systems for various infectious diseases. They contain various phytochemicals that exhibit antimicrobial activities against various bacteria, fungi, and parasites. The mechanisms of their antimicrobial action may involve the disruption of microbial cell walls and membranes, the inhibition of microbial enzyme and biofilm formation, the modulation of microbial gene expression and quorum sensing, and the induction of microbial cell death. Therefore, the present study evaluated the potentials of aqueous and ethanol extracts of S. cumini, M. oleifera, and T. cordifolia in managing infections as measured by their inhibitory effects on species. Materials and method Syzygium cumini, M. oleifera, and T. cordifolia were obtained and authenticated, and their aqueous and ethanol extracts were prepared. The antibacterial properties of the aqueous and ethanol extracts were examined. In addition to broth microdilution and biofilm development experiments, we also employed disk diffusion and agar-well diffusion techniques. The inocula of various species, including krusei, parapsilosis, utilis, albicans, and glabrata, were prepared for these assays. The synergistic effect of plant extracts with fluconazole was also evaluated. Results Syzygium cumini, M. oleifera, and T. cordifolia emerge as promising sources for the development of effective and sustainable antimicrobial interventions. Interestingly, the aqueous and ethanol extracts were effective against the selected species. Also, the synergistic combination of plant extracts with fluconazole was observed to triple the potency of the extracts. Furthermore, the potency of the plant extract as an antifungal and synergistic agent was ranked as S. cumini > M. oleifera > T. cordifolia. Conclusively, the plant extracts are effective in the management of opportunistic fungal infections.
... Jamun juice is often mixed with mango juice and it acts as a very good drink for quenching thirst in the diabetic patient. Water diluted juice is used as a gargle for soar throat and as a lotion for ringworm of the scalp (Katiyar et al., 2016) [14] . Fruits are also a rich source of iron; thus, it ensures the supply of properly oxygenated blood throughout the body (Joshi et al., 2001) [13] . ...
... Jamun is rich in iron, hence it can truly act as a blood purifier, so that there will be enough production of haemoglobin. Hence it acts as a protective food for menstruating women (Katiyar et al., 2016) [14] . ...
... Jamun is rich in iron, hence it can truly act as a blood purifier, so that there will be enough production of haemoglobin. Hence it acts as a protective food for menstruating women (Katiyar et al., 2016) [14] . ...
Article
Full-text available
Jamun (Syzygium cumini) commonly known as Indian blackberry is an important fruit of Indian sub-continent and belongs to Myrtaceae family. Jamun has been proved to be a boon to human kind since time immemorial. Every part of the Jamun tree has high medicinal value, right from its fruit to its seed and bark to the leaves. It is an important fruit crop of Indian subcontinent, under-exploited and widely grown successfully due to its wider adaptability and nutraceutical properties. Fruits contain various types of antioxidants, flavonoids, phenolics, carotenoids and vitamins, which are all beneficial to human health. Jamun has also anti-diabetic, anticancer, antiviral, antibacterial and anti-hyper lipidemic properties. Fruits of Indian black berry are effectively in blood purifying. Seeds are effectively in anti-diabetic and leaves are effectively in strengthing the teeth. Jamun fruit is rich in antioxidants which can boost immune system, aid in digestion, relieve stomach pain, reduce flatulence and prevent infections. Jamun has astringent properties and keeps skin healthy. They are also used in nutrition, herbal medicine and cosmetics. The present review has been made to access several bioactive compounds and health benefits of Jamun.
... It was exported to Thailand, Madagascar, the Philippines, Israel, Algeria, California, Ceylon, Malaya, and Australia, among other nations. (Katiyar et al, 2016) [24] The evergreen tree is grown throughout the entire south Indian forested region. It is grown in Thailand, the Deccan, Bengal, the Philippines, Madagascar, the Philippines, Thailand, as well as by streams and in wet areas of evergreen forests. ...
... It was exported to Thailand, Madagascar, the Philippines, Israel, Algeria, California, Ceylon, Malaya, and Australia, among other nations. (Katiyar et al, 2016) [24] The evergreen tree is grown throughout the entire south Indian forested region. It is grown in Thailand, the Deccan, Bengal, the Philippines, Madagascar, the Philippines, Thailand, as well as by streams and in wet areas of evergreen forests. ...
... The decrease in the percentage of parasitemia and the increase in the percentage of inhibition are caused by bioactive compounds that have antimalarial activity contained in Syzygium cumini including alkaloids, flavonoids, tannins (Katiyar et al., 2016;Panghal et al., 2019). The antimalarial effect of tannin compounds works in the asexual phase of erythrocytes by inhibiting Plasmodium from infecting erythrocytes, resulting in reduced erythrocyte destruction and decreased invasion of new erythrocytes which prevents increased parasitemia in mice. ...
... The decrease in the percentage of parasitemia and the increase in the percentage of inhibition are caused by bioactive compounds that have antimalarial activity contained in Syzygium cumini including alkaloids, flavonoids, tannins (Katiyar et al., 2016;Panghal et al., 2019). The antimalarial effect of tannin compounds works in the asexual phase of erythrocytes by inhibiting Plasmodium from infecting erythrocytes, resulting in reduced erythrocyte destruction and decreased invasion of new erythrocytes which prevents increased parasitemia in mice. ...
... Syn. Eugenia jambolana), otherwise called Indian blackberry, is being claimed to have a positive effect in reducing the plasma blood sugar level in diabetic patients and also can be utilized in conditions/complications related to diabetes (Katiyar et al., 2016). Its fruits and seeds are reported to have antidiabetic properties and are used in treating diabetic mellitus in folklore medicine. ...
Article
Full-text available
Jamun (Syzygium cumini Linn. Syn. Eugenia jambolana) genotypes collected from different parts of the country were evaluated for in vitro alpha-glucosidase inhibitory activity, polyphenolic content and antioxidant potential along with fruit characters. Results indicated significant variation among genotypes for fruit characters, phenolics, flavonoids, antioxidant potential, and alpha-glucosidase inhibitory potential. Total phenolics and flavonoids in seeds varied between 15.5 mg to 98.7 mg GAE/g and 0.79 mg to 9.03 mg CE/g seeds, respectively. The seeds with a high content of polyphenolic compounds required a very less amount of sample to inhibit alpha-glucosidase enzyme. The genotype Selection 45 recorded the highest alpha-glucosidase inhibitory activity, and required only 50.3 µg of sample to inhibit 50 % of the enzyme activity. Both phenolics and flavonoids content positively correlated with antioxidant potential and negatively correlated with enzyme inhibitory potential. From cluster analysis, the genotypes AJG-85, Kaithanal, Selection-45, Collection-2, and Konkan Bahdoli were identified as superior genotypes having a considerable amount of seeds with alpha glucosidase inhibitory compounds. These genotypes/collections may be effectively utilized for further studies to isolate and characterize the bioactive constituents with alpha-glucosidase inhibitory potential.
... The leaves are loaded with myricitin, esterase, acylated flavonol glycosides, tannins, myricetin, and galloyl carboxylase (Katiyar et al., 2016). In cultured human peripheral blood cells, it is discovered that the leaves lessen radiation-induced DNA damage . ...
Chapter
Tropical fruit Syzygium cumini, also referred to as jamun, is a native of the Indian subcontinent, is widely planted throughout numerous continents due to its extraordinary capacity to adapt to various climatic conditions. From India to Southeast Asia, where nations like Bangladesh, Sri Lanka, and Myanmar are included, is where its native range is found with a long history of traditional medicinal use. Due to its adaptability and ability to survive in a variety of environments, jamun trees are a common fruit crop in Asia, Africa, and some regions of South America. In the summer, they produce dark-purple berries that are not only delicious but also nutrient-dense. Jamun offers a wide range of health advantages because of its abundance in antioxidants, dietary fiber, vitamins, and minerals. Because it improves insulin sensitivity and blood sugar regulation, research suggests it may be useful in the management of diabetes. Additionally, the abundance of antioxidants in jamun fights oxidative stress and inflammation, possibly lowering the risk of chronic illnesses. Its dietary fiber aids in weight control and supports digestive health. Jamun also has anti-viral, anti-microbial, and even potential anti-cancer capabilities. It may also strengthen the immune system, promote cardiovascular health, and support cardiovascular health. Although jamun has many health benefits, it should be used in moderation as part of a balanced diet, taking into account individual variances and any sensitivities. Overall, the widespread use, adaptability, and exceptional health benefits of jamun highlight its value as a fruit with a significant capacity to improve people's well-being.
Chapter
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Diabetes is a prevalent health issue worldwide. The traditional agents used to prevent diabetes originate from India. The most used tree species in India for treating diabetes and other health issues is Syzygium cumini. It provides economic and ecological benefits as well. Considering this, an effort has been made to compile the data on S. cumini that is presented in the present study.
Article
Full-text available
The purple color of the ripe Eugenia jambolana fruit is attributed to anthocyanins, a class of plant pigments that has attracted immense attention due to the potential health benefits of these compounds. There is disagreement in the literature on whether E. jambolana fruit anthocyanins are found as 3,5- or 3-diglucosides. Therefore, we used a combination of HPLC-UV, tandem LC-MS, and NMR techniques to identify the structures of anthocyanins present in E. jambolana fruit collected in the U.S.A. and India. Our results indicate that the anthocyanins from both locations occur as 3,5-, but not 3-diglucosides, of delphinidin, cyanidin, petunidin, peonidin, and malvidin. This is the first report to use a combination of spectrometric and spectroscopic methods to identify unequivocally the structures of E. jambolana fruit anthocyanins.
Article
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Syzygium jambos (L.) Alston (Myrtaceae) (syn Eugenia jambos) is a widespread medicinal plant traditionally used in sub-Saharan Africa to treat several diseases. The analgesic potential of leaf hydro-alcoholic extracts was assessed in rats. Hot plate and formalin tests were used to estimate cutaneous nociception whereas measurements of forelimb grip force were done to assess muscular nociception under normal and inflammatory conditions. In the hot plate test, Syzygium jambos extract produced a significant increase in the withdrawal response latencies in a dose-dependant manner (10-300 mg/kg i.p.) and with a maximal effect (analgesic efficacy) similar to that of morphine. The extract (100-300 mg/kg i.p.) significantly reduced pain scores in all the phases of the formalin test with an analgesic efficacy higher than that shown by diclofenac. Although the extract (300 mg/kg) did not alter grip force in intact rats, it reversed the reduction in grip force induced by bilateral injection carrageenan in the forelimb triceps. This analgesic effect of the extract on muscle hyperalgesia was not antagonized, but enhanced, by naloxone. Thus, the Syzygium jambos extract has remarkable analgesic effects on both cutaneous and deep muscle pain that is not mediated by opioid receptors.
Article
The aim of the present study was to investigate the hypoglycaemic and antihyperglycaemic effect of Syzgium cumini (S. cumini) bark in diabetic rats. Diabetes was induced in male albino Wistar rats by a single intraperitoneal injection of streptozotocin (45 mg kg-1 body weight). An aqueous extrzict of S. cumini bark (SBEt) was administered orally. (75, 150 and 300 mg kg-1 body weight) for 45 days and changes in blood glucose, urine sugar, food and fluid intakes and body weight were examined in diabetic rats. Glibenclamide was used as a standard reference drug. The levels of blood glucose and urine sugar were increased significantly in diabetic rats. Oral administration of SBEt to diabetic rats led to significantly decreased levels of blood glucose and urine sugar. The effect exerted by the extract at a dose of 300 mg kg-1 body weight was greater than that of doses 75 and 150 mg kg-1 body weight. The daily food and fluid intakes were significantly increased while the body weights were significantly reduced in diabetic rats when compared to normal rats. Treatment with SBEt significantly restored the above physiological parameters to near normal in streptozotocin diabetic rats. During oral glucose tolerance test (OGGT), long-term administration of SBEt was able to significantly decrease the blood glucose concentrations at 30, 60, 90 and 120 min when compared to the OGTT pattern of diabetic rats. The effect of SBEt at 300 mg kg-1 body weight was better than glibenclamide (600 μg kg-1 body weight). These results suggest that SBEt possesses a significant antidiabetic effect by attenuating the above biochemical and physiological alterations in streptozotocin diabetes. Further, our findings revealed the possible therapeutic value of S. cumini bark for the better control, management and prevention of diabetes mellitus progression.
Article
The efficacy of Momordica charantia (MC), Eugenia jambolana (EJ), Tinospora cordifolia (TC) and Mucuna pruriens (MP) was assessed in the prevention of murine alloxan dibetic cataract. Alloxan (120 mg/kg) was used as the diabetogenic agent. While controls and diabetic controls did not receive any plant extract, treated rats received lyophilized aqueous extract of MC and EJ (200 mg/kg p.o.), alcohol extract of TC (400 mg/kg) and MP (200 mg/kg p.o.) every day until 4 months. Serum glucose concentration was assessed and cataracts examined with both the naked eye and through a slit lamp. Of the eight animals in the diabetic control group, four developed cortical cataract (stage IV) by day 90 while the remaining four developed it by day 100. The incidence rate of cataract in MC, EJ, TC and MP treated groups at 120 days was only 0, 0, 1 and 2. Oral feeding of MC, EJ, TC and MP extracts for 1 month produced a fall of 64.33%, 55.62%, 38.01% and 40.17%, respectively, in the serum glucose levels in comparison with the 48 h level. After 2 months of treatment, the respective values were 66.96%, 59.85%, 40.41% and 45.63%. MC and EJ prevented the development of cataract while the protective effect was less with TC and MP along with a significant reduction of plasma glucose levels (p < 0.001).
Article
Syzygium cumini, Indian black plum or Java plum, is a rich source for anthocyanins (230 mg/100g DW) showing high antioxidant activity in vitro. In the following study it is further demonstrated that S. cumini peel extract rich in anthocyanins (SCA) offers considerable protection against carbon tetrachloride (CCl(4))-induced damage in rat hepatocytes. SCA itself being non-toxic to primary rat hepatocytes at concentrations ranging from 50 to 500 ppm, was found to suppress CCl(4)-induced LDH leakage by 54% at 50ppm, thereby improving the cell viability by 39%. The SCA significantly reversed the CCl(4) induced changes in cellular glutathione (GSH) level, lipid peroxidation and activity of the antioxidant enzyme glutathione peroxidase. Exposure of hepatocytes to SCA after CCl(4) treatment was found to elevate GSH and GPx activities by 2-folds, whereas the activities of catalase and superoxide dismutase were not significantly affected. The fruit pulp extract (SPE) was less effective in offering protection to rat hepatocytes, particularly in terms of total GSH content and a consequent increase in lipid peroxidation although the higher GPx activity suggests the probable involvement of GSH as a substrate for GPx. These observations suggest that the fruit peel extract of S. cumini, is largely responsible for the reversal of CCl(4)-induced oxidative damage in rat hepatocytes. Both peel and pulp extract appear to offer protection to rat hepatocytes through GPx along with other biological pathways independent of catalase and superoxide dismutase.
  • B Sharma
  • G Viswanath
  • R Salunke
  • P Roy
Sharma B, Viswanath G, Salunke R, Roy P, Food Chem., 2008, 110, 697−705.
  • R Sood
  • D Swarup
  • D Bhatia
  • D D Kulkarni
  • S Dey
  • M Saini
  • S C Dubey
  • Ind
Sood R, Swarup D, Bhatia D, Kulkarni DD, Dey S, Saini M, Dubey SC, Ind. J. Exp. Biol., 2012, 50, 179-18.
  • P S Benherlal
  • C Arumughan
Benherlal PS, Arumughan C, J. Sci. Food & Agri., 2007, 87, 2560−2569.
  • M S Balinga
  • H P Bhat
  • Brv Balinga
  • R Wilson
  • P L Palatty
Balinga MS, Bhat HP, Balinga BRV, Wilson R, Palatty PL, Food Res. Int., 2011, 1-14.
  • I M Villasenor
  • M R Lamadrid
Villasenor IM, Lamadrid MR, J. Ethnopharmacol., 2006, 104, 129−131.