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www.wjpps.com Vol 5, Issue 12, 2016.
Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
REVIEW ON CUCUMIS MELO: ETHNOBOTANY AND UNANI
MEDCINE
*Nazeem Fahamiya1, Mohd Aslam2, Aisha Siddiqui2 and Mohamed Shiffa1
1Institute of Indigenous Medicine, University of Colombo, Rajagiriya, Sri Lanka.
2Department of Ilmul Advia (Pharmacology), Faculty of Medicine (Unani), Jamia Hamdard,
New Delhi - 110062, India.
ABSTRACT
Cucumis melo which is commonly known as musk melon belongs to
the family Cucurbitaceae and it is known as kharbuzah in Unani
medicine. It is an annual climbing or creeping herb with angular,
scabrous stem, simple soft hairy orbicular-reniform leaves and bears
tendrils, by which it is readily trained over trellises. The aim of this
review is to explore information available in Unani medicine and
ethnobotanical literatures. Musk melons are extensively cultivated
throughout India particularly in the hot and dry North-Western areas.
Propagation is done by seeds and vegetative method. Main parts used
are pulp, root, seeds and seed oil. It is having diuretic, emmenagogue,
cooling, demulcent, aphrodisiac, galactagogue and astringent
properties. Fruit has been used for several centuries to treat kidney disorders such as kidney
and bladder stones, painful and burning micturition, ulcers in the urinary tract, suppression of
urine and to treat cough, bilious diseases, hot inflammation of the liver, liver and bile
obstruction, eczema, etc. The oil from seeds is said to be very nourishing and contains
linoleic acid (60-70%), lecithin, cephalin and cerebroside isolated from seed oil. The seeds of
melon contain multiflorenol, isomultiflorenol, 24-methylenecycloartenol, α- and β-amyrin,
teraxerol, lupeol, euphol, 24-methyl-25(27)-dehydrocycloartanol, 24-methylene-24-
dihydrolanosterol, 24-methylene-24-dihydroparkeol, tirucallol and cycloartenol. Its
antimicrobial, antioxidant, anti-hyperlipidemic, anti-inflammatory, analgesic, diuretic,
thyroid stimulatory, anthelmintic¸ nephroprotective and cytotoxic activity have been proved
by research studies.
WORLD JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES
SJIF Impact Factor 6.041
Volume 5, Issue 12, XXX-XXX Review Article ISSN 2278 – 4357
*Corresponding Author
Dr. Nazeem Fahamiya
Institute of Indigenous
Medicine, University of
Colombo, Rajagiriya, Sri
Lanka.
nfahamiya@gamil.com
Article Received on
06 October. 2016,
Revised on 26 October 2016,
Accepted on 16 Nov. 2016
DOI: 10.20959/wjpps201612-8223
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Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
KEYWORDS: Cucumis melo, Musk melon, nephroprotective, Unani.
INTRODUCTION
Cucumis melo Linn. belongs to the family Cucurbitaceae. It is an annual climbing or creeping
herb with angular, scabrous stem, simple soft hairy orbicular-reniform leaves and bears
tendrils, by which it is readily trained over trellises. Flowers are unisexual and yellow.
Cucumis melo is extensively cultivated for its fruits, eaten as a vegetable in many tropical
countries. Sometimes it is naturalized in open scrub forests.[1-3]
The many varieties of melon show great diversity in foliage and still more in the size and
shape of the fruit, which in some kinds is as small as an olive and in others it is as large as the
gourd; some are globular, others egg-shaped, spindle-shaped or serpent like, the outer skin
smooth or netted, ribbed or furrowed and variously coloured. The flesh is white, green, or
orange when ripe, scented or scentless, sweet or insipid; some are bitter and even
nauseous.[2,4]
Cucumis melo is known as Kharbuzah in Unnai medicine. It has been used for several
centuries to treat kidney disorders such as kidney and bladder stones, painful and burning
micturition, ulcers in the urinary tract, suppression of urine and to cure cough, bilious
diseases, hot inflammation of the liver, liver and bile obstruction, eczema, etc.[1,5-8]
PLANT TAXONOMY
Kingdom - Plantae Plants
Division - Magnoliophyta
Class - Magnoliopsida
Order - Cucurbitales
Family - Cucurbitaceae
Genus - Cucumis
Species - Cucumis melo Linn
Synonyms - Cucumis callosus (Rottl.) Cogn., Cucumis trigonus Roxb.
VERNACULAR NAMES
Afghanistan - Sardapaliz, Sirdapaliz; Arabic - Battigh, Dummeiri, Kauun; Bengal - Kakri,
Kakur, Kharmuj, Phuti; Bombay - Chibuda, Kakadi, Kharabuja; Burma – Takhva; Chinese -
Kan, Kua, Tien Kua; Danish – Melon; Dutch – Meloen; English - Melon, Sweet Melon;
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French- Melon; German – Melone; Gujarat - Chibdu, Shakarateti, Tarbucha; Hindi - Kakri,
Kharbuja, Khurbuj, Tuti; Italian - Pepone, Popone; Japan - Mukuwauri, Tenkwa; Malaya -
Tien Kua, Tien Kwa; Persian - Kharbuzeh; Russian – Melon; Sanskrit - Amritavha, Ervaru,
Kalinga, Kharbuja, Madhupaka, Shadbhuja; Spanish - Melon, Melon muscatel; Sudan –
Tagesrarit; Swedish – Melon; Tamil - Kakarikkai, Vellarikkai; Urdu – Kharbuzah.[1-3, 9-11]
HABITAT
Cucumis melo is extensively cultivated in gardens as well as in the sandy basins of rivers. Its
centre of origin is supposed to be Africa. It is mentioned in some books as native of South
Asia, which has come from the foot of the Himalayas to Cape Comorin, where it grows wild
but it’s cultivated in the temperate and warm region of the whole world.[4] Domestication of
musk melon may have occurred independently in India, especially North and central India.
Many forms of melons varying in size, skin, pulp-colour and taste are cultivated in North and
Central India.[2,3,9,12,13]
CULTIVATION, PROPAGATION AND COLLECTION
Musk melons are extensively cultivated throughout India particularly in the hot and dry
North-Western areas. Musk melons are grown with magnetically treated water showed higher
yields, higher sugar contents and better colour than those grown with ordinary water.
Propagation is done by seeds and vegetative method and an alternative method is through
tissue culture.[2,3,10,12,14]
PLANT DESCRIPTION
This is an annual climbing herb with angular and scabrous stem.[1-3] Leaves are about 7.5 cm,
orbicular-reniform in outline, 5 angled or lobed, scabrous on both surfaces and also often
with soft hairs, lobes neither deep nor acute and 5 cm long petiole.[1-3, 14] Fruits are spherical
ovoid elongate or contorted, glabrous or somewhat hairy, neither spinous nor tuberculate[1]
and 5 cm long and 4 cm in diameter, yellow with age with green stripes when young. Seeds
are obovoid and rounded at apex. Give fruits in August and September.[2] Flowers are small,
yellow, unisexual flowers contain bells shaped corollas, male flowers borne in small clusters
and female solitary. Male flowers have three stamens, whereas the female flowers have the
ovary and three cells. In central India flowering is between July and August.[2-4, 14]
PARTS USED
Fruit pulp, root, seeds and seed oil.[1,2,6-8]
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CHEMICAL CONSTITUENTS
Meloside A, meloside L and their caffeoyl ester have been isolated from leaves. Α-carotene,
β-carotene, C-carotene and three more carotenes are also isolated.[9, 15] Sulphur compounds
(mostly thioesters) are responsible for the characteristic aroma of the fruits. 3-
Methylpropanenitrile originating from 2-methyl-thiothyglucosinolate through the action of
myrosinase thioglucoside glucohydrolase is a glucosinolate. The existence of myrosinase
activity in fruit is because of 3- methylpropanenitrile. This activity seems to increase with the
maturation of the fruit. Also, maximum activity of the l-amino cyclopropane-l-carboxylate
oxidase was observed in the enzyme extracted from ripe melon fruits to which bicarbonate/
CO2 have been added.[1,3,12]
Fruits contain ferulic, caffeic and chlorogenic acids. Fruit stalk contains cucurbitacin B and
E.[9] Fruit has urease, peptedase, protease and Vitamin A, B, C.[16] Volatile compounds of
cucumber and musk melon were analysed and methyl-2-methylbutaoate-(2)-3 hexanal, 2-
hexanal, and ethyl-2 methyl propane were identified as the primary odorants. Ethyl 3-
propanate and 3-(methyl thio) propyl acetate have been considered to be of importance of
aroma profile of the fruits. The green notes of musk melon are because of -2- and -3-hexenal,
1,8-cineol and -1, 5-octadien-3-one.[3,12]
Methanolic extract of Cucumis melo fruit contains a saponin (C40H64O16, mp, 158-59˚)
which is identified as stigmasta-7-16-25(26) triene-3-O-β-D-glucopyranosyl (15)-O-β-D-
xylofuranoside. Presence of curcumin and leptodermin is also reported in the fruits.[12]
Linoleic acid (60-70%), lecithin, cephalin and cerebroside isolated from seed oil. The seeds
of melon contain multiflorenol, isomultiflorenol, 24-methylenecycloartenol, α- and β-amyrin,
teraxerol, lupeol, euphol, 24-methyl-25(27)-dehydrocycloartanol, 24-methylene-24-
dihydrolanosterol, 24-methylene-24-dihydroparkeol, tirucallol and cycloartenol.[15]
In Cucumis melo seeds, Codisterol, 25(27)-dehydroporiferasterol, avenasterol, clerosterol,
isofucosterol, stigmasterol, campesterol, sitosterol, 25(27)-dehydrochondrillasterol, 24β-
ethyl-25-(27)-dehydrolathosterol, 24ξ-methyllathosterol, spinasterol and 22-
dihydrospinasterol were identified.[15] Cucurbit seeds are promising substitutes for various
nuts in milk beverages. This is supported by evidence on the high enzyme activities of urease,
lipase, lipoxygenase, trypsin inhibitors and low activity of β-amylase in musk melon. The
seeds contain triterpenoid glucoside.[3,12,17] The protein content of seed meal 49.93%. The
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seed contain myristic acid, phosphates, galactane, lysine, citrulline, histidine, tryptophane,
cystine.[16]
UNANI PERSPECTIVE
Temperament (Mizaj)
Cold2 and moist2[5, 7, 18] Hot1 and moist2[6, 8, 19-21]
Adverse Effects (Muzir Asrat)
The fruits may cause allergy, congestion of eyes in plethoric people, headache, bilious fever,
diarrhea and indigestion.[1,21,22] Also produce adverse effects on spleen and spleenic disorders
and is not suitable for old persons and cold temperament people.[8,21] Its excess use causes
adverse effect on stomach and intestine.[20]
Corrective (Musleh)
Following drugs have been recommended to be used along with Kharbuza to avoid its
adverse effects which act as correctives. They are Shahad (honey),[8,21] Banafsha (Viola
odorata),[8,20] Zarish (Berberis vulgaris),[20] Sounf (Foeniculum vulgare),[20] Salt and
Sugar.[21]
Substitute (Badal)
The following drugs are mentioned in the Unani text as substitutes for Kharbuza. They are
Tukhm-e-Kheyareen (Cucumis sativus),[20,21] Badam shereen (Prunus amygdalus)[20] and
Chilgoza (Pinus gerardiana).[20]
Formulations (Murakkabat)
Banadiq-e-Buzoor,[19] Habb-e-Nafs-ud-Dam Silli,[24] Halwa-e-Salab,[24] Jawarish-e-Zaruni,[6]
Jawarish-e-Zarroni Ambari,[24] Labube-e-Barid,[6] Majoon-e-Hajral Yahud,[6] Majoon-e-
Kaknaj,[24] Majoon-e-Muravvahul Arvah,[6] Majoon-e-Salab,[23] Muffareh Barid Sada,[23]
Qurs-e-Kafoor,[6] Qurs-e-Sartan,[6] Qurs-e-Sartan-Kafoori,[24] Sharbat Bazuri Barid,[19]
Sharbat-e-Mudir,[6] Sharbat Bazuri Motadil,[6] Tiryaq-e-Masana.[23]
Therapeutic Dose (Miqdar-e-Khurak)
The therapeutic doses mentioned by various authors are as 7 – 15 g,[8] 7 – 12 g,[20] and 5 – 7
g.[21]
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Pharmacological actions of Kharbuza
Lachrymatory (Dhalka),[1] diaphoretic (Moarriq),[1] detergent (Jali),[6-8,18,19] cooling
(Mubarrid),[1-3,13,17] Diuretic (Mudir-e-Baul),[1-8,13,17-21] emmenagogue (Mudir-e-Haiz),[19, 21]
liver deobstruant (Mufatteh-e-Jigar),[5,8,19,20] lithotriptic (Mufattit-e-Hisat),[5,6,14,19,21] nutritive
(Mughazzi),[1,3,10,11,13] laxative (Mulayyan),[1,3,5,8] concoctive (Munzij),[8] demulcent
(Mulattif),[9,10,13] strengthen the heart, brain and body (Muqawwi-e-Qalb, Dimagh wa
Badan),[1,3,14] aphrodisiac (Muqawwi-e-Bah),[1,3,8,14] emetic (Muqee),[4,9,12,16] cleansing the
kidney and bladder (Musaffi-e-Kulliya wa Masana),[5,8,20] urinary tract and uterus analgesic
(Musakkin-e-Majarebole wa Reham),[8] purgative (Mushil),[4,9,13] fattening (Musammin-e-
Badan),[1] appetizer (Mushtahi),[3,4,14,16] galactagogue (Muwallid-e-Laban),[1,3,6,20] flatulence
(Muwallid-e-Riya)[20] and astringent (Qabis).[1,3]
Therapeutic uses of Kharbuza
Ophthalmia (Amraz-e-Ain),[1-3,12] liver disorders (Amraz-e-Jigar),[1,3,5,8] kidney disorders
(Amraz-e-Kuliya),[1,3,8,14] chronic and bilious fevers (Khuna wa safravi humma),[1,3,5,8,19]
cough due to heat (Garm Khansi),[5] painful and burning micturition (Hirquat-ul-
Baul),[1,3,5,8,20] burning sensation of the oesophagus (Hirquat-ul-Mari),[1,20] kidney and bladder
stones (Hisat-e-Kuliya wa Masana),[5-7,19,20] ascites (Istisqa),[1,3,6] burning sensation
(Jalan),[2,3] insanity (Janoon),[1,3,9] improving complexion (Mumallisat-e-jild),[20] chronic and
acute eczema (Muzmin wa Haad Naar-e-Farsi),[1,9,10,13] suppression of urine (Quilat-e-
Baul),[1,10,13,19] liver and bile obstruction (Tasuddud-e-Kabid wa Safra),[13] biliousness
(Safravi Amraaz),[1,20] vitiligo (Bars),[5,8,18] gonorrhoea (Suzak),[19,20] fatigue (Thakawat),[1]
thirst (Uttas),[1,3,5,8] chest pain (Wajaus Sadar),[5,8,20] inflammation and ulcers in the urinary
tract (Warm wa Qurooh-e-Majar-e-Bole),[6,9,19] hot inflammation of the liver (Warm-e-Jigar
Har),[5, 20] bronchitis (Warm-e-Shobatyn),[1,3,14] dryness of the throat and tongue (Yaboosat-e-
Halaq wa Lisaan),[5,8] jaundice (Yarqan),[6] sexual tonic and semen producing (Zau-e-Baah
wa Muzayyad-e-Mani),[20] general debility (Zauf-e-Amoomi)[3,14] and dyspepsia (Zauf-e-
Hazm).[1,3,13,14]
RESEARCH STUDIES ON CUCUMIS MELO
Phytochemical studies
Terpenoid profile of Cucumis melo (L). was elucidated using high performance thin layer
chromatography (HPTLC). The Rf value of the different compounds present in the extract
was found to 0.06, 0.21 and 0.93 of peak 1, 2 and 3 respectively. Among them, peak 1 was
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found to be terpenoid compounds. C. melo fruit extract showed the presence of terpenoids
and it was confirmed from the chromatogram after derivatization.[25]
The morphological, microscopic, physicochemical and chromatographic studies were carried
out by Fahamiya et al (2012) developed quality control parameters for Cucumis melo Linn.[26]
Sasi Kumar (2014) identified ten compounds in ethanolic extract of Cucumis melo, 5-
hydroxy -6,7,8-trimethoxy-2,3-dimethyl-4H-chromen-4-one (21.04%) was the major
proportion.[27] The effect of freeze-drying on the antioxidant compounds and antioxidant
activity tests showed that there were no significant (p < 0.05) differences found between the
fresh and freeze-dried fruit of muskmelon in the amounts of total phenolic compounds (TPC)
and change observed in the ascorbic acid content.[28]
The methanolic extract of the seeds of Cucumis melo L. var. reticulatus (Cucurbitaceae)
afforded three new chromone derivatives; 5,7-dihydroxy-2-[2-(4-hydroxyphenyl) ethyl]
chromone, 5,7-dihydroxy-2-[2-(3,4-dihydroxyphenyl)ethyl] chromone and 7-glucosyloxy-5-
hydroxy-2-[2-(4-hydroxyphenyl)ethyl] chromone, together with three known compounds;
beta-amyrin, beta-sitosterol and beta-sitosterol-3-O-beta-glucopyranoside.[29]
A new phenolic glycoside (E)-4-hydroxycinnamyl alcohol 4-O-(2′-O-β-D-apiofuranosyl)
(1″→2′)-β-D-glucopyranoside was isolated and identified from Cucumis melo seeds together
with benzylO-β-D-glucopyranoside, 3,29-O-dibenzoylmultiflor-8-en-3α,7β,29-triol and 3-O-
p-amino-benzoyl-29-O-benzoylmultiflor-8-en-3α,7β,29-triol.[30]
21 cucurbitane-type triterpenoids, including nine new compounds and 12 known compounds
were isolated and identified from the stems of Cucumis melo. Two known compounds,
cucurbitacin B and cucurbitacin A showed significant cytotoxic activity against the
proliferation of A549/ATCC and BEL7402 cells in vitro. Of the new compounds, only
compound 7 was weakly cytotoxic.[31]
The seeds contained high percentages of lipids (35.36%) and proteins (29.90%). Hexane-
extracted oil had acid, peroxide, iodine and saponification values of 1.51, 3.95, 89.5 and
226.73, respectively. Gas chromatographic analysis of the oil revealed the presence of
twenty-five fatty acids varying from C4 to C24 with the exception of C5, C7, C11 and C19.
Linoleic, oleic, palmitic and stearic acids were the principal fatty acids and had a relatively
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high percentage of unsaturated fatty acids. Seed proteins were rich in arginine, aspartic and
glutamic acids while limiting amino acids were methionine and lysine.[32]
Partial purification and characterization of three alpha-galactosidases, including a novel
alkaline alpha-galactosidase (form I) from melon (Cucumis melo) fruit tissue was carried out
by Gao and Schaffer (1999).[33] The form I enzyme showed preferred activity with raffinose
and significant activity with stachyose. Other unique characteristic of this enzyme is weak
product inhibition by galactose.
From the seeds of Cucurbitaceae fourteen dihydroxy triterpenes and their derivatives and one
oxo-sterol were characterized. They are 7-oxodihydrokarounidiol-3-benzoate, isokarounidiol-
3-p-methoxybenzoate, karounidiol-3-benzoate, karounidiol, isokarounidiol, 5-
dehydrokarounidiol, 7-oxodihydrokaroudnidiol, bryonolol, 3-epibryonolol, loranthol, betulin,
29-hydroxylupeol, erythrodiol, (23Z)-cycloart-23-ene-3beta,25-diol and 7-oxositosterol
among which the first two were the new naturally occurring compounds. Karounidiol and 7-
oxodihydrokarounidiol were detected in all of the investigated seed materials.[34]
Cucumisin (EC 3.4.21.25) isolated from prince melon fruit is a plant serine protease. Its milk-
clotting activity was compared with plant cysteine proteases such as papain (EC 3.4.22.2) and
ficain (EC 3.4.22.3). Cucumisin was more stable than papain under the condition of pH 7.1,
37ºC for 24 h. The milk-clotting activity of cucumisin was same to that of papain and was
half value of that of ficain.[35]
Two squash family trypsin inhibitors, CMeTI-A and CMeTI-B, were isolated from the melon
(Cucumis melo) seeds, by ion exchange chromatography, gel filtration, affinity
chromatography and high-performance liquid chromatography and their amino acid
sequences were determined. All inhibitors contain 29 amino acid residues including 6 half-
cystine residues.[36]
Triterpene alcohols in the seeds of two Cucumis species of cucurbitaceae. Isomultiflorenol
was the major component accompanied by its Δ17-isomer, multiflorenol, in the triterpene
alcohol fractions of the unsaponifiable.[37]
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Pharmacological studies
Antimicrobial activity
The aqueous, heptane, petroleum ether and acetone extract of the whole plant of Cucumis
melo L., Pergularia daemia Frosk. (Asclepiadaceae) was screened for the antibacterial and
antifungal activity by Hemantkumar (2015).[38] Highest zone of inhibition was shown by
whole plant and fruit extract of Cucumis melo L. with aqueous and acetone with C. albicans
and E. coli 08 and 12 mm respectively. Very poor response was observed with acetone and
aqueous extract in other bacterial and fungal stains. Highest zone of inhibition was shown by
whole extract of Pergularia daemia with heptane with E. coli and C. albicans, 16 and 21 mm
respectively.
Sasi Kumar (2014), found that the extract and fractionates of fresh fruits of Cucumis melo
showed a significant and remarkable activity against all the microorganisms. Based on the
antioxidant analysis obtained, it was showed that the extract of Cucumis melo fruits exhibits
the greatest antioxidant activity through the DPPH radicals scavenging activity.[27]
Antioxidative and cytotoxic activity
A study was conducted to determine the activity of Cucumis melo extract and β-carotene in
antioxidative and cytotoxic potencies by Wahyu Widowati (2015).[39] The study was done by
examining the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity assay.
C. melo extract showed more active anti-cancer both in HeLa (IC50: 23.649 μg/mL) and
HepG2 (IC50: 110.403 μg/mL) cancer cells. C. melo extract (IC50: 16,670.404 μg/mL) and
β-carotene (IC50: 50,645.994 μg/mL) had low cytotoxicity in NIH3T3 fibroblast. C. melo
extract has lower antioxidant activity, but higher cytotoxic potency compared with β-
carotene.
Vasundra Devi (2011) found that the Cucumis melo possessed Ferric Reducing Antioxidant
Power and was found to possess cytotoxic effect against Ehrlich’s Ascites Carcinoma
cells.[40] The in vitro cytotoxicity of the aqueous extract of Cucumis melo against Ehrlich’s
Ascites Carcinoma cells were done at different concentrations for a period of 3 hours
treatment. The aqueous extract of Cucumis melo showed cytotoxic effect against the
Ehrlich’s cancer cells in a dose dependent manner. As the concentration of the extract
increased the cytotoxicity also increased.
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Dose-dependent cytotoxic activities were exhibited by human prostate carcinoma PC-3 cell
line with aqueous fruit extract of Cucumis melo. As the dose of the extract is increased, the
numbers of viable cells are decreased. This confirms that the anti-cancer and cytotoxic
potential of the fruit of C. melo.[41]
Anti-hyperlipidemic activity
Bidkar (2012) found that the treatment with Cucumis melo fruit peel (CMFP) methanolic and
aqueous extract showed significant (P<0.01) reduction in gain in body weight, serum lipid
profile like total cholesterol (TC), triglyceride (TG), low density lipoprotein cholesterol
(LDL-C) level, atherogenic index and increased the serum high density lipoprotein
cholesterol (HDL-C) levels in 28 days treatment when compared to the hyperlipidemic
control group.[42] The fecal excretion of bile acids and sterols were further increased upon
treatment with CMFP methanolic and aqueous extract and standard drug. Administration of
methanolic extract of CMFP at a dose of 500 mg/kg showed higher antihyperlipidemic
activity as compared to other extract treated groups.
Vitiligo
An open observational study to evaluate the efficacy and safety of the investigated product
containing phenylalanine, Cucumis melo extract and acetyl cysteine, given alone or in
combination with 311-nm narrow band microphototherapy, excellent repigmentation (>75%)
was achieved by 38-73% of patients, depending on the treatment regimen. Mild to moderate
side effects were observed only in patients treated with clobetasol 0.05% ointment. The tested
gel formulation showed a good efficacy in improving vitiligo repigmentation. No side effects
were observed.[43]
Antioxidant activity
The seed extract was found to have significant scavenging activity 75.59% at 300 μg mL-
1 by 1, 1-dipheny1-2-picrylhydrazy1. picrylhydrazyl method and 69.86% at 400 μg mL-1 by
Hydrogen peroxide method as compared to standard (ascorbic acid).[44]
A melon (Cucumis melo LC.) pulp concentrate (MPC) rich in superoxide dismutase (SOD)
activity was tested for its ability to decrease stress protein expressions along the
gastrointestinal tract in a swine model. A SOD-rich MPC provided at the dose of 50 IU/kg of
food for up to 12 d was effective in lowering the level of stress proteins along the
gastrointestinal tract of pigs after weaning.[45]
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After 14 days of oral administration of 1250 mg of the melon extract/gliadin or vehicle,
animals underwent 30 min of thoracic aortic cross-clamping and 4 h of reperfusion. The
melon extract/gliadin blunted the DNA damage, reduced spinal cord apoptosis and attenuated
NO release, however, without any effect on lipid peroxidation and organ function. Pre-
treatment with the oral melon extract/gliadin may be a therapeutic option to reduce oxidative
cell injury affiliated with aortic cross-clamping.[46]
Oxykine is the cantaloupe melon extract rich in vegetal superoxide dismutase covered by
polymeric films of wheat matrix gliadin. Study carried out by Naito et al. (2005) showed that
the treatment of oxykine ameliorated the progression and acceleration of diabetic
nephropathy for rodent model of type 2 diabetes.[47] These results indicated that the oxykine
reduced the diabetes-induced oxidative stress and renal mesangial cell injury.
The Cucumis melo L. extract (CME) inhibited in a dose-dependent manner the production of
superoxide anion with a maximal effect at 100 mcg/ml. This inhibitory effect of CME
appeared to be closely linked to the SOD activity because it was dramatically decreased after
heat inactivation of the SOD activity (HI-CME). When the SOD activity was present in the
CME it promoted the IgG1IC-induced production of IL-10 instead of TNF-alpha.[48]
Anti-inflammatory and analgesic activity
As far as anti-inflammatory is concerned, the maximum percentage inhibition by rat paw
edema was 61.6% at 300 mg kg-1 observed. Further the extract showed maximum analgesic
activity i.e. 70.6% at 300 mg kg-1 by acetic acid induced writhing method and increased the
pain threshold significantly after 60 min at 300 mg kg-1 by tail immersion method.[44]
Diuretic and nephroprotective effects
The diuretic effects of the ethanolic seed extracts of Macrotyloma uniflorum and Cucumis
melo in Albino rats were evaluated by measuring the urine volume, Sodium, Potassium,
Chloride and Bicarbonate contents. A significant diuretic effect was observed from the
experimental animals treated with extracts of Macrotyloma uniflorum and Cucumis melo
individually compared to the control. Further, extract of Cucumis melo (400mg/kg) showed
more diuretic effect than standard.[49] Pharmacodynamic investigations into the diuretic
activity of Cucumis melo seed (ether extract) has been done by Singh and Sisodia (1970).[50]
Jawarish Zarooni Sada (JZS) is one such polyherbal preparation containing 15 ingredients,
mainly described to be diuretic and nephroprotective. Ethanol and water extracts of JZS
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Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
(300 mg each) were investigated for diuretic activity by measuring the total urine output over
a period of 6 h. Sodium and potassium level in urine sample was also estimated.
Nephroprotective activity of JZS against gentamicin-induced nephrotoxicity was investigated
by administering JZS along with high dose of gentamicin (40 mg/kg) and elevation of serum
urea and serum creatinine was taken as the index of nephrotoxicity. JZS showed significant
diuretic and nephroprotective effect.[51]
Gentamicin treated group showed increased levels of blood urea nitrogen and serum
creatinine, which were significantly retrieved in group pretreated with methanolic extract of
Cucumis melo (ME-CM) seed kernel. The level of superoxide dismutase, catalase,
glutathione peroxidase and reduced glutathione were increased with decrease in
malondialdehyde content in ME-CM pretreated group when compared with gentamicin alone
treated group. The histopathological analysis also showed the protective nature of ME-CM in
gentamicin-induced renal damage.[52]
Thyroid stimulatory and antiperoxidative activity
Administration of peel extracts Cucumis melo (CM) fruits significantly increased both the
thyroid hormones (T 3 and T 4) with a concomitant decrease in tissue LPO. In serum lipid
profile CM reduced the concentrations of total cholesterol and low-density lipoprotein-
cholesterol. The results revealed that the thyroid stimulatory and antiperoxidative role of peel
extracts of Cucumis melo fruits.[53]
Anthelmintic property
Zinchenko et al. (1955) found anthelmintic pryoperties in Cucumis melo seeds.[54]
Inhibits human platelet aggregation
An active fraction was isolated from an aqueous melon extract (Cucumis melo) and was
shown that it inhibits human platelet aggregation induced by epinephrine, ADP, collagen,
thrombin, sodium arachidonate, prostaglandin endoperoxide analogue U-46619 and PAF-
acether.[55]
CONCLUSION
Cucumis melo which is known as kharbuzah in Unnai medicine has been used for several
centuries to treat different kinds of ailments by Unani physicians. There are large number of
phytoconstituents have been discovered. However, very few pharmacological studies have
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Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
been carried out to prove its beneficial effects scientifically. Hence, this review will serve as
base for further studies to validate the claims mentioned in the Unani medicine and
ethnobotanical literatures.
CONFLICT OF INTEREST: None.
REFERENCES
1. Kirtikar KR, Basu BD. Indian Medicinal plants. Vol. II, 2nd ed, Dehra Dun: International
Book Distributors: 1987; 1140 –1142.
2. Parrotta JA. Healing plants of peninsular India. USA: CABI Publishing: 2001; 254- 255.
3. Prajapati ND, Purohit SS, Sharma AK, Kumar T. A handbook of medicinal plants. India,
Agrobios: 2001; 176.
4. Biswas PK. Encyclopaedia of medicinal plants. Vol. III, New Delhi, Dominant publishers
and distributors: 2006; 584, 585.
5. Ibn-e-Baitar, Aljamaiul Mufradat-ul Advia Wal Aghzia. V.I (Urdu Trans), New Delhi,
CCRUM: 2003; 248- 252.
6. Kabiruddin M. Makhzanul Mufradat. Lahore, Sheikh Mohammad Bashir & Sons: 1951;
265-266.
7. Ibn-e-Rushd AWMB. Kitabul kuulliyat (Urdu Trans). New Delhi, CCRUM: 1987; 255.
8. Hakeem MA. Bustan-ul Mufradat. Lucknow, Idara Taraqqi Urdu Publications: 1311 H.
p159.
9. Joshi SG. Medicinal plants. New Delhi, Oxford & IBH publishing Co. Pvt. Ltd: 2000;
156.
10. Chopra RN, Chopra IC, Handa and Kapoor. Chopra’s indigenous drugs of India. 2nd ed,
Calcutta, UN Dhur and Sons Private Ltd: 1958; 502.
11. .The useful plants of India. New Delhi Publication & information directorate, council of
science & industrial research: 1992; 149.
12. The wealth of India. Vol. II, New Delhi, National institute of science communication,
Council of science & industrial research: 2001; 252, 253.
13. Nadkarni KM. Indian Materia Medica. Vol. I, Bombay, Popular Prakashan: 1989; 402,
403.
14. Pullaiah T. Encyclopaedia of world medicinal plants. Vol. II, New Delhi, Reagency
publication: 2006; 674, 675.
www.wjpps.com Vol 5, Issue 12, 2016.
Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
15. Rastogi RP, Mehrotra BN. Compendium of Indian Medicinal Plants. Vol. II (1970-1979),
Lucknow, Central Drug Research, and New Delhi, Publication & Information
Directorate: 1991; 228.
16. Perry LM. Medicinal plants of east and Southeast Asia. Cambridge, London, MIT Press:
1980; 253.
17. Trease GE, Evans WC. Pharmacognosy. London, New York, W.B. Saunders: 2002; 473.
18. Ibn-e-Sina. Alqanoon Fit Tibb (Urdu Translation by Ghulam Hussain Kantoori), vol. II,
Lahore, Sheikh Mohannad Bashir & Sons: 1927; 55.
19. Ram Labaya. Goswami Bayanul Advia. Vol I, Delhi, Goswami Pharmacy: 1984;
232-234.
20. Ghani MN. Khazain-ul-Advia. Lahore, Pakistan, Sheikh Basheer Ahmad & Sons: 1920;
495- 498.
21. Rafiquddin M. Kanaz-ul-Advia Mufradah. Aligarh, Muslim University Press: 1985;
322,323.
22. Besler M. Paschke A, Rodríguez J. Allergen Data Collection: Melon (Cucumis melo)
Matthias. Internet Symposium on Food Allergens, 2001; 3(3): 143-151.
23. Arzani MA. Qarabadeen-e-Qadri. New Delhi, CCRUM: 2009.
24. National formulary of Unani medicine. Part I, Vol. II, New Delhi, Department of
AYUSH: 2007.
25. Vidya R, Kalaivani K, Venkatesh R. Phytochemical Standardization of Cucumis melo(L).
Extract by HPTLC Techniques. Am. J. Pharm Tech Res., 2014; 4(4): 344 -350.
26. Fahamiya N, Mohammed Aslam, Aisha Siddiqui, Mohamed Shiffa. Pharmacognostical
study and development of quality control parameters for Cucumis melo Linn. Am. J.
Pharm Tech Res., 2012; 2(4): 1-14.
27. Sasi Kumar R, Priyadharshini S, Nandha Kumar KPL, Nivedha S. In Vitro
pharmacognostical studies and evaluation of bioactive constituents from the fruits of
Cucumis melo L (Muskmelon). International Journal of Pharmacognosy and
Phytochemical Research, 2014 -15; 6(4): 936-941.
28. Shofian NM, Hamid AA, Osman A, Saari N, Anwar F, Dek MS, Hairuddin MR. Effect of
freeze-drying on the antioxidant compounds and antioxidant activity of selected tropical
fruits. Int J Mol Sci., 2011; 12(7): 4678-92.
29. Ibrahim SR. New 2-(2-phenylethyl)chromone derivatives from the seeds of Cucumis
melo L var. reticulatus. Nat Prod Commun., 2010; 5(3): 403-6.
www.wjpps.com Vol 5, Issue 12, 2016.
Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
30. De Marinoa S, Festaa C, Zolloa F, Iorizzi M. Phenolic glycosides from Cucumis
melo var. inodorus seeds. Phytochemistry Letters, 2009; 2(3): 130-133.
31. Chen C, Qiang S, Lou L, Zhao W. Cucurbitane-type triterpenoids from the stems
of Cucumis melo. J Nat Prod., 2009; 72(5): 824-9.
32. Mian-hao H, Yansong A. Characteristics of some nutritional composition of melon
(Cucumis melo hybrid ‘ChunLi’) seeds. International Journal of Food Science &
Technology., 2007; 42(12): 1397–1401.
33. Gao Z, Schaffer AA. A novel alkaline alpha-galactosidase from melon fruit with a
substrate preference for raffinose. Plant Physiol., 1999; 119(3): 979-88.
34. Akihisa T, Kimura Y, Kasahara Y, Kumaki K, Thakur S, Tamura T. 7-
oxodihydrokarounidol-3-benzoate and other triterpenes from the seeds of cucurbitaceae.
Phytochemistry, 1997; 46(7): 1261-1266.
35. Uchikoba T, Kaneda M. Milk-clotting activity of cucumisin, a plant serine protease from
melon fruit. Applied Biochemistry and Biotechnology, 1995; 56(3): 325-330.
36. Lee CF, Lin JY. Amino acid sequences of trypsin inhibitors from the melon Cucumis
melo. J Biochem., 1995; 118(1): 18-22.
37. Itoh T, Shigemoto T, Shimizu N, Tamura T, Matsumoto T. Triterpene alcohols in the
seeds of two Cucumis species of cucurbitaceae. Phytochemistry, 1982; 21(9): 2414-2415.
38. Hemantkumar A. Thakur. Antimicrobial and antifungal activity of Cucumis melo l.
(cucurbitaceae) and Pergularia daemia frosk. (asclpiadaceae) an ethnomedicinal plants.
International Journal of Bioassays, 2015; 4(1).
39. Wahyu Widowati, Rachma Micho Widyanto, Dian Ratih Laksmitawati, Pande Putu
Erawijantari, Laura Wijaya, Ferry Sandra. Phytochemical, free radical scavenging and
cytotoxic assay of Cucumis melo l. extract and β-Carotene. Journal of Advanced
Agricultural Technologies, 2015; 2(2): 114-119.
40. Vasundra Devi PA, Sharmila S, Divyapriya S. Invitro cytotoxicity and free radical
scavenging activity of aqueous extract of Cucumis melo. IJPBR, 2011; 2(6): 150-156.
41. Ittiyavirah Sibi P, George Ann, Santhosh Anju M, Kurian Sudhi T, Pappachan Prinsy,
Jacob Gifty. Studies of cytotoxic potential of Cucumis melo. linn fruit aqueous extract in
prostate cancer cell lines PC-3 Using MTT and neutral red assay. Iranian Journal of
Pharmacology & Therapeutics, 2013; 12(1): 24-29.
42. Bidkar JS, Ghanwat DD, Bhujbal MD, Dama GY. Anti-hyperlipidemic activity of
Cucumis melo fruit peel extracts in high cholesterol diet induced hyperlipidemia in rats. J
Complement Integr Med., 2012; 24(9).
www.wjpps.com Vol 5, Issue 12, 2016.
Nazeem et al. World Journal of Pharmacy and Pharmaceutical Sciences
43. Buggiani G, Tsampau D, Hercogovà J, Rossi R, Brazzini B, Lotti T. Clinical efficacy of a
novel topical formulation for vitiligo: compared evaluation of different treatment
modalities in 149 patients. Dermatol Ther., 2012; 25(5): 472-6.
44. Arora R, Kaur M, Gill NS. Antioxidant activity and pharmacological evaluation
of Cucumis melo var. agrestis methanolic seed extract. Phytochemistry, 2011; 5(3):
146-155.
45. Lallès JP, Lacan D, David JC. A melon pulp concentrate rich in superoxide dismutase
reduces stress proteins along the gastrointestinal tract of pigs. Nutrition, 2011; (3):
358-63.
46. Kick J, Hauser B, Bracht H. Effects of a cantaloupe melon extract/wheat gliadin
biopolymer during aortic cross-clamping. Intensive Care Med., 2007; 33(4): 694-702.
47. Naito Y, Akagiri S, Uchiyama K, Kokura S. Reduction of diabetes-induced renal
oxidative stress by cantaloupe melon extract/gliadin biopolymers, oxykine, in mice.
Biofactors., 2005; 23(2): 85-95.
48. Vouldoukis I, Lacan D, Kamate C, Coste P, Calenda A, Mazier D, Conti M, Dugas B.
Antioxidant and anti-inflammatory properties of a Cucumis melo LC. extract rich in
superoxide dismutase activity. J Ethnopharmacol, 2004; 94(1): 67-75.
49. Ravishankar K, Vishnu Priya PSV. Evaluation of diuretic effect of ethanolic seed extracts
of macrotyloma uniflorum and Cucumis melo in rats. Int J Pharm Bio Sci, 2012; 3(3):
251- 255.
50. Singh RC, Sisodia CS. Pharmacodynamic investigations into the diuretic activity
of Cucumis melo seed (ether extract). Indian J Med Res., 1970; 58(4): 505-12.
51. Afzal M, Khan NA, Ghufran A, Iqbal A, Inamuddin M. Diuretic and nephroprotective
effect of Jawarish Zarooni Sada—a polyherbal unani formulation. J Ethnopharmacol.,
2004; 91(2-3): 219-23.
52. Nazeem Fahamiya, Mohd. Aslam, Kalim Javid, Aisha Siddiqui, Mohamed Shiffa.
Nephroprotective activity of methanolic extract of Cucumis melo Linn. In gentamicin
induced nephrotoxicity, IJDFR, 2012; 3(2): 40-53.
53. Parmar HS, Kar A. Possible amelioration of atherogenic diet induced dyslipidemia,
hypothyroidism and hyperglycemia by the peel extracts of Mangifera indica, Cucumis
melo and Citrullus vulgaris fruits in rats. Biofactors, 2008; 33(1): 13-24.
54. Zinchenko TV, Mindlin MZ, Prokopovich NN. Anthelmintic Properties of Cucumis
melo Seeds. Farmakol Toksikl, 1955; 18(5): 41-3.