+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
HOSTED BY
Available online at www.sciencedirect.com
ScienceDirect
Food Science and Human Wellness xxx (2014) xxx–xxx
Food prospects and nutraceutical attributes of Momordica species: A
potential tropical bioresources – A review
∗
Gunasekaran Nagarani, Arumugam Abirami, Perumal Siddhuraju
Bioresource Technology Lab, Department of Environmental Sciences, School of Life Sciences, Bharathiar University, Coimbatore 641 046, Tamil Nadu, India
Received 25 February 2014; received in revised form 27 June 2014; accepted 3 July 2014
Abstract
Plants with potential therapeutic values have been used from time immemorial to cure various ailments and infectious diseases. Of late, scientific
evidences have been provided on the potential therapeutic agent exhibited by certain traditionally used vegetable extracts. The importance of
wild edible plants may be traced to antiquity but systemic studies are recent. All the Momordica species have been consumed as vegetable and
traditionally used for various disorders. The whole plant parts are ascribed to possess the anti-diabetic effect in traditional medicinal system. The
active constituents of Momordica plant parts were cucurbitane type triterpenoids, phenolics, glycosides, and several kinds of peptides including
Momordica anti-HIV protein (MAP 30). Recent reports revealed the presence of several kinds of cucurbitane type triterpenoids in leaf, stem and
fruits of Momordica species having several pharmacological activities. There is lack of scientific information available on the wild species which
also having several bioactive components with potential activities. So the present review compares and highlights the current knowledge of the
nutritional value, phytochemistry and physiological effects of wild species with known variety.
© 2014 Beijing Academy of Food Sciences. Production and hosting by Elsevier B.V. All rights reserved.
Keywords: Momordica spp.; Anti-diabetic; Triterpenoids; Momordica anti-HIV protein (MAP-30 protein)
Contents
1. Introduction ...... 00
2. Biogeography and botanical description ...... 00
3. Nutritional values ...... 00
4. Bioactive compounds ...... 00
4.1. Phenolics compounds ...... 00
4.2. Carotenoids ...... 00
4.3. Cucurbitane type triterpenoids ...... 00
4.4. Phytosterols ...... 00
5. Effect of physiological bioactivities of Momordica species on human health ...... 00
5.1. Anti-diabetic activity ...... 00
5.2. Anti-cancer activity ...... 00
5.3. Antioxidant activity ...... 00
5.4. Anti-microbial activity...... 00
5.5. Other medicinal effects ...... 00
6. Conclusions ...... 00
Acknowledgment ...... 00
References ...... 00
∗
Corresponding author at:. Tel.: +91 422 2428394; fax: +91 422 2422387.
E-mail addresses: [email protected], [email protected] (P. Siddhuraju).
Peer review under responsibility of Beijing Academy of Food Sciences.
2213-4530 © 2014 Beijing Academy of Food Sciences. Production and hosting by Elsevier B.V. All rights reserved.
http://dx.doi.org/10.1016/j.fshw.2014.07.001
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
2 G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx
1. Introduction M. balsamina is restricted to the arid belt zones such as Rajasthan
and Gujarat, while M. cymbalaria is distributed in Andhra
Momordica species are vegetable crops, belonging to the Pradesh, Karnataka, Madhya Pradesh and Maharashtra. M.
family of Cucurbitaceae (also commonly referred as cucumber, sahyadrica is a recently described species [9] and is endemic
gourd, melon or pumpkin family), which comprise of medium to the Western Ghats of India. In general, these plants are com-
sized plants that grow abundantly in warmer regions of the world. monly annuals or perennials. Leaves are entire or deeply lobed
They are well-known for the bitter taste due to the presence of (3–7). Flowers are monoecious or dioecious, solitary/pseudo
phytochemicals (alkaloid) and have a wide range of medicinal raceme, medium to big size, with foliaceous bracts, corolla
values. Although the exact origin of Momordica genus is unclear, creamish yellow to bright yellow color, green to pale green
most experts agree that the center of bitter gourd domestication stigma (in monoecious species) or yellow (in dioecious species).
lies in eastern Asia, possibly eastern India or southern China Fruits are medium to big sized (5–800 g), fleshy, green when
[1,2]. However, in Ayurvedic texts written by members of the unripe and orange red when ripe, ovoid oblongoid, ornamented
Indo-Aryan culture, it is stated to be emerged in India from 2000 with soft spines, warts or tubercles, splits from base into three
to 200 BCE [3]. Consumption of Momordica species as vegeta- valves. Seeds are enclosed in orange red sarcotesta (aril), and
bles is mainly concentrated in Africa and Asian countries. The sculptured, margins often undulate and dentate [10].
fruits are usually parboiled or soaked in salt water before cooking
to reduce the bitter taste [4]. The Momordica species have
been used in indigenous medical systems in various countries 3. Nutritional values
in Asia and Africa. Based on the indigenous knowledge, wild
plant foods play a vital role in the complex cultural system of The mature green fruit of the Momordica species is the most
tribal people for reducing various disorders. Research has shown commonly consumed portion of the plant, although the tender
that many edible wild plants are rich in specific constituents, leaves of M. balsamina can be cooked as a leafy vegetable pro-
referred as phytochemicals, which may have health promoting viding an important source of nutrients [11]. These green fruits
effects. The major plant-derived chemical groups in this fam- and leaves are a good source of carbohydrates, proteins, vita-
ily now recognized as having potential health promoting effects mins and minerals (Table 1). The protein content of this species
in Type I and Type II diabetes are cucurbitane triterpenoids, makes it a good source of essential amino acids (Table 2) such
saponin glycosides and Momordica anti-HIV protein (MAP 30 as methionine, phenylalanine, alanine, serine, cystine and thre-
protein). These phytochemicals may be incorporated into food onine compared to other vegetables and traditional protein-rich
stuffs or food supplements as nutraceuticals. The green fruits legumes [4]. Differences in the agro-climatic conditions may
and leaves of Momordica species play a major role in improving account for the variation in the protein contents in this species.
human health by offering nutritional and nutraceutical compo- Hassan and Umar [11] have studied the nutritional values of M.
nents. Therefore the present review mainly focuses on providing balsamina leaves. In comparison with other species, M. balsam-
baseline information on exploring nutritional and nutraceutical ina leaves have more dietary fiber (29%) and mineral contents
properties of some wild plant species along with cultivated vari- (Table 1) while Momordica fruits have moderate content of
ety of Momordica species such as M. charantia, M. balsamina dietary fiber, which helps to lower the blood cholesterol. M.
(Linn), M. dioica (Roxb), M. cochinchinensis (Spreng), and M. balsamina leaves are labeled as a heart protective leafy veg-
tuberosa or cymbalaria. Fig. 1 shows the green fruits of five dif- etable because of its high content of potassium (1320 mg/100 g)
ferent species in this genus. This study highlights the potential that helps to maintain normal blood pressure and other cardio-
of Momordica species as an important source of both nutritional vascular conditions [12]. The trace element, zinc, has also been
and bioactive compounds. In addition, this study also supports reported in fruits and leaves of Momordica species (Table 1).
the inclusion of these wild species into the main food stream of
the local population, improving their nutritional status.
4. Bioactive compounds
2. Biogeography and botanical description
Momordica plant parts are characterized by a wide diver-
Based on both historical literature [1,2,5], and recent anal- sity of bioactive compounds such as phenolic acids, flavonoids,
ysis of random amplified polymorphic DNA [6], inter simple carotenoids cucurbitane triterpenoids, and phytosterols. The
sequence repeats [7] and amplified fragment length polymor- potential health benefits of phytochemicals found in Momordica
phisms [8] molecular analyses, eastern India (including the states species have received ample attention in the recent literature,
of Orissa, West Bengal, Assam, Jharkhand and Bihar) may be focusing especially on compounds with high antidiabetic, antitu-
considered as the primary center of the diversity of bitter gourd, mor and antioxidant properties. In particular, some of the actual
where a wild feral form, M. charantia varieties also exists. trends of the scientific research are strongly focused on obtaining
M. dioica and M. charantia are ubiquitous in distribution over in vitro evidence for the biological efficacy of individual con-
India except in north-east region, whereas M. subangulata ssp. stituents such as triterpenoids, carotenoids and phenolics from
Renigera is restricted to north-east and adjoining north Ben- different parts of Momordica spp. Around 228 different com-
gal hills. M. cochinchinensis is distributed in Andaman and a pounds were identified from different parts of M. charantia [13].
few of regions in the eastern and north eastern states of India. However, with regard to these various bioactive substances of
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx 3
Fig. 1. Green fruits of different Momordica species.
M. charantia, only limited information was found on the wild stilbenes and ligans [14]. The polyphenols found in food can help
species due to limited habitat and lack of awareness. to protect oxidative damage by acting directly on reactive oxygen
species and induce endogenous defense system. Phytochemistry
4.1. Phenolics compounds analysis of different plant parts of Momordica species revealed
the presence of flavonoids, coumarins, anthroquinones, antho-
Phenolic compounds are chemical substances considered as cyanins and phenolic acids [15]. Various types of phenolic acids
major secondary metabolites of plant origin having more than such as gallic acid, protocatechuic acid, gentisic acid, vanillic
one phenol group per molecule. Phenolics are classified into two acid, chlorogenic acid, tannic acid, caffeic acid, p-coumaric acid,
categories as flavonoids and non flavonoids. Flavonoids share a p-hydroxybenzoic acid, gentisic acid, chlorogenic, syringic acid,
basic structure consisting of two benzene ring linked through a ferulic and sinapic acid were identified in the pericarp, pulp and
heterocyclic prone C ring whereas non flavonoids phenolics con- seeds of M. charantia and M. cochinchinensis fruits. The content
tains the heterogenous group of compounds. The non flavonoid of these compounds vary among different parts and species. M.
compounds are further classified into phenolic acids, tannins, charantia is a rich source of gallic acid in all parts such as leaf
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
4 G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx
Table 1
Proximate and mineral composition of Momordica fruit.
Compositions M. charantia M. dioica M. balsamina M. cymbalaria M. cochinchinesis
Moisture/% 93.20 84.1 71.00 84.30 88.6
Ash/% 7.36 6.7 18.00 – –
Lipids/% 6.11 4.7 2.66 – 0.1
Fiber/% 13.60 21.3 29.00 6.42 1.1
Protein/% 27.88 19.38 11.29 2.15 1.5
Carbohydrate/% 34.31 47.92 39.05 12.60 7.6
Energy kcal/100 g 241.66 311.5 189.22 73.00 37.0
Calcium mg/100 g 20 33 941 72.00 64.0
Magnesium mg/100 g – – 220 – –
Sodium mg/100 g 2.40 1.51 122.49 40.00 –
Potassium mg/100 g 171.00 8.25 1320.00 500.00 –
Iron mg/100 g 1.8 4.6 60.3 1.70 0.34
Zinc mg/100 g – – 3.18 2.82 –
Manganese mg/100 g 0.08 – 11.6 0.32 –
Copper mg/100 g 0.19 – 5.44 0.18 –
Phosphorus mg/100 g 70 42 130.46 0.46 89.0
Vitamin C mg/100 g 96 – – 290 0.04
Behera et al. [4]; Hassan and Umar [11].
(95.8 mg/L), stem (72.8 mg/L), green fruit (95.6 mg/L) and ripe fractions of M. cochinchinensis. The phenolic content of bitter
fruit (202 mg/L) [16]. According to Horax et al. [17], gentisic gourd fruits are determined by various factors such as the cul-
acid is also the predominant phenolic acid in M. charantia where tivar, agronomic management, climatic factors, developmental
it accounts maximum for 72.8 mg/100 g in immature green fruits stage, harvesting time, storage conditions, and postharvest man-
and 214.6 mg/100 g in seeds but vanillic acid and t-cinnamic agement. Most studies have investigated the functional activities
acid were found lower in comparison to other phenolic acids. of bitter melon fruits, leaves and stems. It has been determined
In the case of wild M. cochinchinensis, ferulic acid has been that the antioxidant capacity of bitter melon fruit is due to their
reported as the predominant phenolic acid in pulp (92.94 mg/L) high phenolic content [17]. Our previous report showed that the
followed by p-hydroxybenzoic acid in pulp (69.31 mg/L) and aril presence of various phenolic acids in the leaves from varieties of
(29.16 mg/L). Vanillic acid has not been found in either parts of M. charantia and M. dioica [18]. Among them the wild leaves
this fruit. Table 3 shows the phenolic acid profiles of various fruit were reported to have higher phenolic acid composition and
Table 2
Comparative account of amino acid composition of Momordica species with WHO adult requirements.
a b
Amino acid M. charantia fruits (mg/g) M. balsamina leaves (mg/g) Amino acid content meeting FAO
c
recommendations (mg/g protein)
Cystine 22.3 5.6 4
Aspartic acid 93.8 82.1 –
Threonine 25.2 31.3 23
Serine 55.0 40.0 –
Glutamic acid 96.0 123.8 –
Proline 54.4 32.1 –
Glycine 44.9 46.6 –
Alanine 51.2 41.6 –
Valine 42.2 41.1 39
Isoleucine 30.8 – 30
Leucine 64.9 83.8 59
Tyrosine 59.4 26.2 38
Phenylalanine 40.2 39.4 38
Methione 27.6 9 16
Histidine 72.8 25.0 15
Lysine 101 39.4 45
Arginine 45.6 48.7 –
Tryptophan – – 6 Note:
a
M. charantia fruit mature pericarp.
b
M. balsamina leaves.
c
Mean nitrogen requirement of 105 mg nitrogen/kg per day (0.66 g protein/kg per day).
Horax et al. [84]; Hassan and Umar [11]; WHO/FAO/UNU [85].
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx 5
Table 3
Phenolic acid composition of different parts with different maturity level of M. cochinchinensis fruits.
Fruit fractions Hydroxybenzoic acids (mg/g) Hydroxycinnamic acids (mg/g) Total mg GAE/g
GA PCCA p-OH VA ChA CFA SyA p-CA FA SNA
Peel (green) 2.46 ND 2.30 ND 0.56 ND ND ND ND ND 5.32
(Yellow) 6.39 ND 6.36 ND 1.97 2.65 ND 4.14 11.32 7.38 40.2
(Red) 2.46 ND 2.30 ND 2.98 2.97 ND ND ND ND 10.7
Pulp (green) 3.09 2.28 60.31 ND ND 2.69 7.19 7.82 92.94 4.56 180.8
(Yellow) 2.57 2.87 2.53 ND ND 2.69 2.25 2.25 7 ND 22.2
(Red) 3.13 ND 2.30 ND 2.82 3.2 3.81 2.24 6 ND 23.5
Aril 4.97 16.15 29.16 ND 1.97 3.41 4.76 11.77 18 4.66 89.9
Note:
GA, gallic acid; PCCA, protocatechuic acid; p-HO, p-hydroxybenzoicacid; VA , vanillic acid; ChA, chorogenic acid; VA , vanillic acid; CFA, caffic acid; SyA, syringic
acid; p-CA, p-coumaric acid; FA, ferulic acid; SNA, sinapic acid; ND, not detected.
Kubola and Siriamornpun [16].
antioxidant activity than those of cultivated variety. Regarding ripen fruit of different species of bitter melon. The amount of
flavonoids the presence of catechin, epicatechin, quercetin, api- carotenoids in Momordica fruit and seeds varied depend upon
genin, myricetin, luteolin and kaempferol has been documented the period of maturation. Lutein and ␣-carotene are impor-
in different varieties on M. charantia and M. cochinchinensis tant groups of carotenoids present in early and mature green
fruit fraction. The inner flesh and aril parts have higher flavonoid fruits. However, zeaxanthin and β-cryptoxanthin are less abun-
content than the other parts of the fruit [16,19]. Kaempferol, lute- dant in early and mid-stage fruits than in mature fruits. A major
olin and apigenin were found only in the wild species but not in carotenoid, lycopene, a red carotenoid, is only accumulated in
M. charantia [20]. The increased level of antioxidant activity of the final stage when the pulp began to turn red [21]. Lycopene
green gac fruits might be caused by the presence of flavonoid found to be high in aril and low in pulp but not detected in seeds
content. Rutin was reported in the M. tuberosa and M. charantia [22]. On the other hand, the content of lutein was found to be rich
whereas absent in M. cochinchinensis fruit. Our previous report in peel (yellow) fractions, which was substantially higher than
on flavonoid composition of Momordica leaves suggested that other fractions. However, the concentrations of each group of
rutin was only found in M. dioica and absent in the other two corotenoids were lower than M. cochinchinensis. Reports sug-
varieties of M. charantia [18]. gest that the intake of lutein or diets supplemented with rich
in lutein such as fruits and vegetables are important for the
4.2. Carotenoids prevention of diseases like some cancers, eye diseases and car-
diovascular diseases [22,23]. In Vietnam, the seed membranes
The ripen fruits of Momordica species contains a wide range of M. cochinchinensis are used to aid in the relief of dry eyes
of carotenoids and are good sources of β-carotene [21], although due to the presence of corotenoids [23].
wild species have been explored for the highest content of
corotenoids. Especially, M. cochinchinensis is very popular for 4.3. Cucurbitane type triterpenoids
its high content of lycopene and β-carotene [22]. Table 4 sum-
Cucurbitane triterpenoids are the main constituents of
marizes the carotenoids content that were found in the analyzed
cucurbitaceae family [24]. They exhibit a broad range of potent
species. The Momordica fruit aril membrane and seed pericarp
biological activities namely hepatoprotective, cytotoxic, anti-
contain highly valuable sources of carotenoids [21]. They are
inflammatory, cardiovascular, anti-diabetic and antiparasitic
responsible for the yellow, orange, and scarlet red colors of
effects [24,25]. The terpenoids, also referred as isoprenoids
which is derived from five carbon isoprene units. The cucur-
Table 4
bitacins are a typical group of cucurbitane type triterpenoids
Carotenoid concentration of M. charantia and M. cochinchinensis seed mem-
brane (g/g fresh weight). found in all plants and belonging to the cucumber family
(Cucurbitaceae) and have been reported as the main chemical
Carotenoid (g/g) M. cochinchinensis M. charantia
constituents of Momordica species from different parts. Bitter
α
-Carotene 4.2 ND
melon contains several groups of triterpenoids including
β-Carotene 61.8 Trace
charantin [26], kuguacins A-S [27], momordicine I, II and III
Lycopene 424.6 261
[28] and karavilagenin A, B, C, D and E [29,30]. Hsu et al. [31]
Zeaxanthin – Trace
E
Lutein 1.1 ND isolated the five new terpenoids namely, cucurbita-6,22( ),
β β
β
Cryptoxanthin 1.9 Trace 24-trien-3 -ol-19,5 -olide, 5 ,19-epoxycucurbita-6,22(E),24-
Xanthophylls 9.9 ND β
triene-3 ,19-diol, 3β-hydroxycucurbita-5(10),6,22(E),24-
Total carotenoids 424.6 261 tetraen-19-al, 19-dimethoxycucurbita-5(10),6,22(E),24-tet-
β
ND, not detected. raen-3 -ol and 19-nor-cucurbita-5(10),6,8,22(E),24-pentaen-
Rodriguez et al. [86]; Vuong et al. [87].
3β-ol. Furthermore, cucurbitane-type triterpene glycosides,
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
6 G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx
charantagenins D and E are isolated from the fruit of M.
charantia L. [32]. Hsiao [33] fractionated 15 cucurbitane-type
triterpene glycosides from methanol extract of M. charantia
fruit. Ma et al. [34] isolated two cucurbitane triterpenoids
and bidesmoside triterpenoid saponins from the seeds of
M. charantia. In addition, leaves also considered as impor-
tant sources of triterpenoids. Zhang et al. [35] isolated
seventeen cucurbitane-type triterpenoids with six new com- β
pounds (23E)-3 ,25-dihydroxy-7 β-methoxycucurbita-5,
23-dien-19-al, (23S*)-3 β-hydroxy-7 β,23-dimethoxy-
cucurbita-5,24-dien-19-al, (23R*)-23-O-methylmomordicine
§
IV, (25 )-26-hydroxymomordicoside L, 25-oxo-27-
normomordicoside L, and 25-O-methylkaravilagenin D.
In addition, two new charantin group triterpenoids charantin A
and charantin B were recently isolated from the leaves of M.
charantia [36]. A number of non-specific measures of saponin
derivatives also exist in Momordica species. Saponins are
steroid or triterpenoid glycosides, common in a large number
of plants and plant products that are important in human and
animal nutrition. These compounds have also been observed to
kill protozoans and molluscs, to be antioxidants, to assist the
digestion of protein and the uptake of vitamins and minerals in
the gut, to cause hypoglycaemia, and to act as antifungal and
antiviral agents [37]. Saponins are a group of high molecular-
weight compounds in which the saccharide units of glycosides
were linked with triterpene groups. charantosides (I–VIII),
momordicosides U, V, and W were some of the major saponins
identified from M. charantia fruits [38,39]. Other types of
saponins like goyasaponins I, II and III have been reported
in the fresh fruit of Japanese M. charantia [40]. Triterpenoid
saponins such as momordicoside M, N, O, and L were generally
predominant in fresh green fruits of M. charantia [41]. The
wild species such as M. balsamina and M. cochinchinensis
are also major sources of triterpenoids. M. balsamina contains
several cucurbitane-type triterpinoids which are isolated from
different parts including balsaminapentaol, balsaminol A,
balsaminol B, cucurbalsaminol A, cucurbalsaminol B [42]. M.
cochinchinensis contained five saponins triterpenoids namely
A, B, C, D and E [43]. The cucurbitane-type triterpenoids were
reported for several medicinal properties such as hypoglycemic,
antiproliferative activities and also used for the treatment of
free radical and reactive oxygen species mediated diseases
[30]. In addition, these compounds were reported as partial
agonist/antagonist for estrogen receptors such as ER␣ and ER
and were used for the management of estrogen related health
problems [44]. Some of the newly identified triterpenoids with Fig. 2. Structure of novel triterpenoids from Momordica species.
their structure are shown in Fig. 2.
4.4. Phytosterols
predominant phytosterols have been identified in Momordica
Sterols cannot be synthesized by humans and are absorbed
species namely, decortinone, decortinol, clerosterol, ergosterol
from the diet in small but significant amounts. Plant sterols
peroxide, 3 β-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one,
have proved to lower serum total and low density lipoproteins
β α
22-diene-3 ,7 -diol, 5 α,6 α-epoxy-(22E,24R)-ergosta-8, 6
(LDL)-cholesterol concentrations, so they have been incor-
α
-epoxy-(22E,24R)-ergosta-8,22-diene-3 β,7 β-diol, 5 α,6 α
porated into functional foods. Sterols are minor components
β α
-epoxy-(22E,24R)-ergosta8,22-diene-3 ,7 -diol, and 5 α,6 α
of human dietary lipids and comprise the major portion of β
-epoxy-3 -hydroxy-(22E,24R)-ergosta-8,22-dien-7-one [45].
the unsaponifiable fraction of most edible fats and oils. Nine
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx 7
5. Effect of physiological bioactivities of Momordica triglycerides and lipoproteins [53,54]. With respect to the clin-
species on human health ical trials, 12-weeks treatment with bitter gourd tablet was
conducted in different groups of patients after normal meals. The
5.1. Anti-diabetic activity study showed that regular consumption of these tablets associ-
ated with positive effects in glucose, cholesterol, HDL, LDL,
Diabetes poses a major challenge and the economic pressure triglyceride levels and had beneficial effects on glucose toler-
to the world population, leading to increasing interest in the use ance [55]. Furthermore, nanoparticles of extract of M. charantia
of traditional remedies for the treatment of diabetes mellitus. and its adsorption on polyethylene glycol (PEG) microspheres
Momordica species are well known for the treatment of dia- are considered as an alternative treatment of diabetes [56].
betes from ancient times and nowadays the tablet forms of bitter Considering all these facts, it can be concluded that Momordica
gourd are also available in the market. Momordica species are has potential anti-diabetic properties, which may suggest the
used for the treatment of both Types I and II diabetes. Insulin is inclusion of this plant in anti-diabetic regimens. However, fur-
the mainstay for patients with type 1 diabetes. Recently, several ther studies in details are warranted to explore the mechanistic
proteins were isolated from M. charantia which were involved and therapeutic potential of Momordica for decreasing serum
in the insulin signaling pathway. Isolated compounds such as glucose concentration in combination with the active phyto-
insulin-like peptide (plant (p)-insulin), charantin, vicine, glyco- chemical substances.
sides, karavilosides, fruit and seed extract, juices and powders
have demonstrated potential effects in lowering blood sugar by 5.2. Anti-cancer activity
increasing glucose uptake and glycogen synthesis in the liver,
muscles, and fat cells and activating insulin receptor substrate In the last few decades, a number of preliminary stud-
1 (IRS1) in skeletal muscle by tyrosine phosphorylation [46]. ies have been carried out to reveal the anti-cancer activity of
Some other reports stated that the hypoglycemic effects might Momordica sp. There are many significant evidences suggest-

be due to the significant increase in cell number, glucose uptake ing links between diets rich in bitter melon and lower risk of
by skeletal muscle and adipose tissue, and activation of AMPK lymphoid leukemia, lymphoma, choriocarcinoma, melanoma,
pathway that stimulates the insulin secretion [47]. Hazarika et al. breast cancer, skin tumor, prostatic cancer, squamous carci-
[48] studied the docking mechanism by block the active site of noma of the tongue and larynx, human bladder carcinomas and
the glycogen synthase kinase-3 (GSK-3) protein with known Hodgkin’s disease [57]. There are some epidemiological evi-
three anti-diabetic compounds namely, charantin, momordenol dence stating that intake of bitter melon are inversely related
and momordicilin. GSK-3 is one of the negative regulators in to the incidence of cancer. Methanol extract of M. charantia
the hormonal control of glucose homeostasis which are involved was shown to inhibit the growth of four human cancer cell lines,
in the carbohydrate metabolism through the mechanism of Hone-1 nasopharyngeal carcinoma cells, AGS gastric adenocar-
phosphorylation and inactivation of the enzyme glycogen syn- cinoma cells, HCT-116 colorectal carcinoma cells, and CL1-0
thase. The novel IR-binding protein (Trypsin inhibitor) was lung adenocarcinoma cells. M. charantia induces cell death by
isolated from aqueous extract of M. charantia seeds, which activating the caspase-3 enzyme and increase the level of apop-
lowered blood sugar levels by regulating the insulin signaling togenic protein and the expression of Bax gene, which induces
pathway in muscles and adipose tissues and stimulating the IR- DNA fragmentation and nuclear condensation [58]. Treatment
downstream pathway [49]. M. charantia extract also considered of fractionated seed extract of M. charantia in human myeloid
β
as an herbal remedy for type-II diabetes, contains a specific 11 - HL60 cells induced the differentiation and can be used as ther-
hydroxysteroid dehydrogenase type 1 inhibitor, responsible for apy for leukemia [59]. Pitchakarn et al. [60] reported that fresh
reducing the PPARA gene expression [46]. Folk wisdom showed bitter melon leaf extract significantly decreased the gene expres-
that Momordica species helps to prevent or counteract Type II sion of MMP-2 and MMP-9 in a breast cancer cell line. It
diabetes, improves glucose tolerance and suppress postprandial has also been found that these extract could increase them
hyperglycemia in rats [50]. Oxidative stress is also one of the RNA level of TIMP-2, known to have inhibitory effects on the
causative mechanisms for diabetes. M. charantia fruit juice is activity of MMP-2. Most attention to date has focused on sev-
reported to restore antioxidant enzymes like superoxide dismu- eral phytoconstituents of Momordica including triterpenoids,
tase and catalase in diabetic patients to the normal level [51]. Kuguacin J, ␣-momorcharin and MAP 30 protein. Fang et al.
Treatment of alloxan induced diabetic rats with bitter melon pre- [61] reported the inhibiting property of MAP 30 protein iso-

vented the death of -cells by decreasing the oxidative stress due lated from seeds of M. charantia against the growth of Hep
to the presence of vitamin C (an anti-oxidant). Feeding saponin- G2 leukemia cells. Moreover, other proteins from M. charantia
rich fraction of M. cymbalaria over a period of one month to seeds were reported to inhibit melanoma proliferation. Xiong
streptozotocin-induced Type II diabetic mice leads to increased et al. [62] isolated a novel ribosome-inactivating protein called
insulin secretion, hepatic glycogen synthesis and attenuation of ␣-momorcharin and -momorcharin from the mature seeds of
hyper insulinemia. Also the treated groups showed an increase in M. charantia which efficiently inhibits the growth of prostate
β
the number of pancreatic islets and -cells in the pancreas [52]. cancer. Manoharan et al. [63] described the mechanisms of this
Treatment with the fruit extract of M. tuberosa and seed extract phytochemical in different cancer cell lines, ␣-momorcharin
of M. dioica has been shown to decrease blood glucose level in and -momorcharin increased the cell death specifically in
diabetic rats with simultaneous reduction in serum cholesterol, cancer cell lines by increasing the caspase-3 and 9 activities,
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
8 G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx
releasing cytochrome c and elevating calcium level. Recently, of 20% (V/V). Purified triterpenoid ester from M. cochinchinen-
Weng et al. [44] isolated a novel cucurbitane-type triterpenoid sis leaves was proved to inhibit Trigrophyton mentagrophytes
(3β, 7β-dihydroxy-25-methoxycucurbita-5, 23-diene-19-al) and Candida albicans [74]. MAP-30 and type-I ribosome inac-
from wild bitter gourd that induces apoptotic death in breast tivating protein from bitter melon reported to have anti-HIV
cancer cells. Ramalhete et al. [64] proved that some novel cucur- activity [75]. Fruit pulp of M. balsamina was found to be
bitacins, balsaminagenin B, balsaminoside A and the known effective against HIV-1 and significantly increased the CD4
cucurbitacin karavelagenin C, together with some new mono or count within the first two weeks of treatment when com-
diacylated derivatives of karavelagenin C from aerial parts of M. pared to the untreated mice [76]. Adesina et al. [77] reported
balsamina strongly inhibited the human MDR1 gene transfected that application of bitter melon leaf powder at the concen-
to mouse lymphoma cells. The seed extracts of M. cochinchi- tration of 2 g greatly reduced Callosobruchus maculates in
nensis have been reported as inhibitors for breast cancer against stored cowpea seeds. Methanol extract of bitter melon leaves
ZR-75-30 breast cancer cells [65]. exhibited strong oviposition deterrent activity against Liriomyza
trifolii females on the host plant leaf when it was dipped in
5.3. Antioxidant activity the methanol extract at a concentration of 1 mg of fresh leaf
equivalent/mL [41].
Oxidative stress is implicated in the etiology of many dis-
eases such as dyslipidaemia, atherosclerosis, obesity, Type II
5.5. Other medicinal effects
diabetes, arthritis, cancer, cardio vascular diseases and neurode-
generative diseases. It is a condition of increased production
Momordica-supplemented foods are considered as good
of free radicals and other reactive oxygen species and decreased
sources of hepatoprotective substances, which can help to pro-
antioxidative defenses [66]. Various extracts of bitter gourd have
tect liver damage by restoring liver markers and preventing the
potential antioxidant activity which might play an important role
lipid peroxidation reaction [78]. Lii et al. [79] reported that wild
in diabetic-related enzymes and individuals with neuroinflam-
bitter melon fruit pulp significantly inhibited lipopolysaccaride-
mation and liver diseases. Nerurkar et al. [67] reported that the
induced inflammatory response in rats. Momordica has potential
administration of bitter melon fruit extract significantly reduced
anti-fertility activity in both male and female mice. It induced
the neurodegenerative diseases as its role as antioxidant to reveal
irregular estrous cycles and suppressed the release of ova and
a mechanism for its neuroinflammation action. Cucurbitane-type
caused highly significant post-coital anti-implantation effect
triterpene glycoside 1 and 3 isolated from stems and fruits of M.
in early stage of pregnant [80]. The glycoprotein, ␣- and -
charantia significantly inhibit the effect on Xanthine oxidase
momorcharins isolated from M. charantia seeds induced the
activity which is the key enzyme for the induction hyperuricemia
testicular degeneration in male animals and the effect was
and gout [68]. Antioxidant compounds in bitter gourd pulp and
reversible within a predictable time frame of 8 weeks after
seed powders showed potential natural antioxidant activity to
discontinuation of the treatment [81]. Analgesic and neuropro-
inhibit the lipid peroxidation in sunflower oil [69]. Moreover,
tective activity were observed in M. dioica fruit and M. charantia
the antioxidant activity of butanol fraction of M. charantia was
fruit juice [82,83].
determined in in vitro and a cellular system and the extract effec-
-
tively ameliorated oxidative damage induced by ONOO [70].
The potential antioxidant activity of M. balsamina has already 6. Conclusions
been reported and its antioxidant components are polyphe-
nols, inhibiting 5-lipo-oxygenase enzyme that is responsible for Momordica species may be considered as a nutritious veg-
inflammation [71]. etable and can play a role in health improving attributes of
As previously stated, bitter gourd was generally consumed their wide range of functional components. The green fruits,
after cooking, so it is important to analyze the effect of heat leaves and stems were rich sources of triterpenoids, carotenoids,
treatment on bitter gourds. Phan-Thi and Wache [72] studied the phenolics that could potentially be used as antioxidants in
effect of heat treatment on lycopene concentration and antioxi- nutraceutical, pharmaceutical, and cosmetic industries. Com-
dant ability. They found that moderate heating transferred all pare to the known common variety, the wild species offers
trans-isomers to cis-isomers leading to increased antioxidant more potential phytoconstituents for improving the human
activity. In the case of M. charantia, blanching considerably health. The regular consumption of these wild bitter gourds
decrease the phenolic content and antioxidant activity which associated with the reduced risk of several chronic diseases
denoted that thermal treatment is more suitable for wild species mainly diabetes for cost effective treatment for rural commu-
compared to commercial variety [73]. nities. The health promoting properties of common cultivated
variety have been demonstrated in both in vitro and in vivo
5.4. Anti-microbial activity studies. However, studies on wild species remain sparse.
Finally, the review undertaken here generated many sugges-
Various broad-spectrum anti-microbial components have tions concerning the nutritional value, bioactive components,
been isolated from Momordica species. M. charantia leaf extract medicinal, nutraceutical and functional food properties of
inhibits Escherichia coli, Klebsiella pneumonia and Bacillus these plant resources may serve as a foundation for future
subtilis with a maximum inhibitory activity at a concentration investigations/interventions.
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx 9
Acknowledgment [20] P.A. Tuan, J.K. Kim, N. Park, et al., Carotenoid content and
expression of phytoene synthase and phytoene desaturase genes in
bitter melon (Momordica charantia), Food Chem. 126 (2011) 1686–
The authors wish to thank University Grants Commission
1692.
(UGC), New Delhi, India (F. No. 34-259\2008) for the financial
[21] J. Kubola, S. Siriamornpun, Phytochemicals and antioxidant activity of
assistance. different fruit fractions (peel, pulp, aril and seed) of Thai gac (Momordica
cochinchinensis Spreng), Food Chem. 127 (2011) 1138–1145.
[22] H. Aoki, M.T.N. Kieu, N. Kuze, et al., Carotenoid pigments in GAC fruit
References (Momordica cochinchinenensis Spreng), Biosci. Biotechnol. Biochem. 66
(2002) 2479–2482.
[1] T.W. Walters, D.S. Decker-Walters, Notes on economic plants. Balsam pear [23] K.B. Ishida, C. Turner, H.M. Chapman, A.T. Mckeon, Fatty acid and
(Momordica charantia, Cucurbitaceae), Econ. Bot. 42 (1988) 286–288. carotenoid composition of Gac (Momordica cochinchinensis Spreng) fruit,
[2] N. Miniraj, K.P. Prasanna, K.V. Peter, Bitter gourd Momordica spp., in: J. Agric. Food Chem. 52 (2004) 274–279.
G. Kalloo, B.O. Bergh (Eds.), Genetic Improvement of Vegetable Plants, [24] Q. Chen, E.T. Li, Reduced adiposity in bitter melon (Momordica charan-
Pergamon Press, Oxford, UK, 1993, pp. 239–246. tia) fed rats is associated with lower tissue triglyceride and higher plasma
[3] D.S. Decker-Walters, Cucurbits, Sanskrit, and the lndo-Aryas, Econ. Bot. catecholamines, Br. J. Nutr. 93 (2005) 747–754.
53 (1999) 98–112. [25] J.L. Rios, J.M. Escandell, M.C. Recio, in: Atta-ur-Rahman (Ed.), Stud-
[4] T.K. Behera, J.K. John, L.K. Bharathi, et al., Chapter 10 Momordica, in: ies in Natural Products Chemistry, vol. 32, Elsevier, Amsterdam, The
C. Kole (Ed.), Wild Crop Relatives: Genomic and Breeding Resources, Netherlands, 2005, p. 429.
Vegetables, Springer-Verlag, Berlin, Heidelberg, 2011, pp. 217–246. [26] J. Pitiphanpong, S. Chitprasert, M. Goto, et al., New approach for extraction
[5] H.L. Chakravarty, Cucurbits of India and their role in the development of of charantin from Momordica charantia with pressurized liquid extraction,
vegetable crops, in: D.M. Bates, R.W. Robinson, C. Jeffrey (Eds.), Biology Sep. Purif. Technol. 52 (2007) 416–422.
and Utilization of Cucurbitaceae, Cornell Univ. Press, Ithaca, New York, [27] J. Chen, L. Lu, X. Zhang, et al., Eight new cucurbitane glycosides,
1990, pp. 325–334. kuguaglycosides A-H, from the root of Momordica charantia L., Helv.
[6] S.S. Dey, A.K. Singh, D. Chandel, et al., Genetic diversity of bitter gourd Chim. Acta 91 (2008) 920–929.
(Momordica charantia L.) genotypes revealed by RAPD markers and agro- [28] M. Yasuda, M. Iwamoto, H. Okabe, et al., Structures of momordicines I, II
nomic traits, Sci. Hortic. 109 (2006) 21–28. and III, the bitter principles in the leaves and vines of Momordica charantia
[7] A.K. Singh, T.K. Behera, D. Chandel, et al., Assessing genetic relationships L., Chem. Pharm. Bull. 32 (1984) 2044–2047.
among bitter gourd (Momordica charantia L.) accessions using inter sim- [29] S. Nakamura, T. Murakami, J. Nakamura, et al., Structures of new
ple sequence repeat (ISSR) markers, J. Hortic. Sci. Biotechnol. 82 (2007) cucurbitane-type triterpenes and glycosides, karavilagenins and karavilo-
217–222. sides, from the dried fruit of Momordica charantia L. in Sri Lanka, Chem.
[8] A.B. Gaikwad, T.K. Behera, A.K. Singh, et al., Amplified fragment length Pharm. Bull. 54 (2006) 1545–1550.
polymorphism analysis provides strategies for improvement of bitter gourd [30] H. Matsuda, S. Nakamura, T. Murakami, M. Yoshikawa, Structures of new
(Momordica charantia L.), Hortic. Sci. 43 (2008) 127–133. cucurbitane-type triterpenes and glycosides, Karavilagenins D and E and
[9] J.K. Joseph, V.T. Antony, Momordica sahyadrica sp. nov. (Cucurbitaceae), karavilosides VI, VII, VIII, IX, X and XI, from the fruit of Momordica
an endemic species of Western Ghats of India, Nord. J. Bot. 24 (2007) charantia, Heterocycles 71 (2007) 331–341.
539–542. [31] C. Hsu, C.L. Hsieh, Y.H. Kuo, C.J. Huang, Isolation and identification of
[10] L.K. Bharathi, A.D. Munshi, S. Vinod, et al., Cytotaxonomical analysis of cucurbitane-type triterpenoids with partial agonist/antagonist potential for
Momordica L. (Cucurbitaceae) species of Indian occurrence, J. Genet. 90 estrogen receptors from Momordica charantia, J. Agric. Food Chem. 59
(2011) 21–30. (2011) 4553–4561.
[11] L.G. Hassan, K.J. Umar, Nutritional value of balsam apple (Momordica [32] X. Wang, W. Sun, J. Cao, et al., Structures of new triterpenoids and cytotox-
balsamina L.) leaves, Pak. J. Nutr. 5 (2006) 522–529. icity activities of the isolated major compounds from the fruit of Momordica
[12] G.S. Thakur, M. Bag, S.B. Sanodiya, et al., Momordica balsamina: a medic- charantia L., J. Agric. Food Chem. 60 (2012) 3927–3933.
inal and neutraceutical plant for health care management, Curr. Pharm. [33] P.S. Hsiao, C.C. Liaw, S.Y. Hwang, et al., Antiproliferative and hypo-
Biotechnol. 10 (2009) 667–682. glycemic cucurbitane type glycosides from the fruits of Momordica
[13] J. Singh, E. Cumming, G. Manoharan, H. Kalasz, E. Adeghate, Medici- charantia, J. Agric. Food Chem. 61 (2013) 2979–2986.
nal chemistry of the anti-diabetic effects of Momordica Charantia: active [34] L. Ma, A.H. Yu, L.L. Sun, et al., Two new cucurbitane triterpenoids from
constituents and modes of actions, Med. Chem. J. 5 (2011) 70–77. the seeds of Momordica charantia, J. Asian Nat. Prod. Res. 16 (2014)
[14] I. Ignat, I. Volf, V.I. Popa, A critical review of methods for characteriza- 476–482.
tion of polyphenolic compounds in fruits and vegetables, Food Chem. 126 [35] J. Zhang, Y. Huang, T. Kikuchi, et al., Cucurbitane triterpenoids from
(2011) 1821–1835. the leaves of M. charantia, and their cancer chemopreventive effects and
[15] P. Daniel, U. Supe, M.G. Roymon, A review on phytochemical analysis of cytotoxicities, Chem. Biodivers. 9 (2012) 428–440.
Momordica charantia, Int. J. Adv. Pharm. Biol. Chem. 3 (2014) 214–220. [36] Y.B. Zhang, H. Liu, C.Y. Zhu, et al., Cucurbitane-type triterpenoids from
[16] J. Kubola, S. Siriamornpun, Phenolic contents and antioxidant activities of the leaves of Momordica charantia, J. Asian Nat. Prod. Res. 16 (2014)
bitter gourd (Momordica charantia L.) leaf, stem and fruit fraction extracts 358–363.
in vitro, Food Chem. 110 (2008) 881–890. [37] G. Francis, Z. Kerem, H.P.S. Makkar, et al., The biological action
[17] R. Horax, N. Hettiarachchy, P. Chen, Extraction, quantification, and antiox- of saponins in animal systems: a review, Brit. J. Nutr. 88 (2002)
idant activities of phenolics from pericarp and seeds of bitter melons 587–605.
(Momordica charantia) harvested at three maturity stages (immature, [38] T. Akihisa, N. Higo, H. Tokuda, M. Ukiya, H. Akazawa, Y. Tochigi, Y.
mature, and ripe), J. Agric. Food Chem. 58 (2010) 4428–4433. Kimura, T. Suzuki, H. Nishino, Cucurbitane-type triterpenoids from the
[18] G. Nagarani, A. Abirami, P. Siddhuraju, A comparative study on antioxidant fruits of Momordica charantia and their cancer chemopreventive effects,
potentials, inhibitory activities against key enzymes related to metabolic J. Nat. Prod. 70 (2007) 1233–1239.
syndrome, and anti-inflammatory activity of leaf extract from different [39] N.X. Nhiem, P.V. Kiem, C.V. Minh, et al., Cucurbitane-type triterpene
Momordica species, Food Sci. Hum. Wellness 3 (2014) 36–46. glycosides from the fruits of Momordica charantia, Magn. Reson. Chem.
[19] O. Kenny, T.J. Smyth, C.M. Hewage, N.P. Brunton, Antioxidant prop- 48 (2010) 392–396.
erties and quantitative UPLC-MS analysis of phenolic compounds from [40] J.Q. Liu, J.C. Chen, F.C. Wang, et al., New cucurbitane triterpenoids
extracts of fenugreek (Trigonella foenum-graecum) seeds and bitter melon and steroidal glycoside from Momordica charantia, Molecules 14 (2009)
(Momordica charantia) fruit, Food Chem. 141 (2013) 4295–4302. 4804–4813.
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
10 G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx
[41] S.Y. Lee, S.H. Eom, Y.K. Kim, et al., Cucurbitane-type triterpenoids in [63] G. Manoharan, S.R. Jaiswal, J. Singh, Effect of ␣,  momorcharin on via-
Momordica charantia, J. Med. Plants Res. 3 (2009) 1264. bility, caspase activity, cytochrome c release and on cytosolic calcium levels
[42] C. Ramalhete, T.A. Mansoor, S. Mulhovo, et al., Cucurbitane-type triter- in different cancer cell lines, Mol. Cell. Biochem. 388 (2014) 233–240.
penoids from the African plant Momordica balsamina, J. Nat. Prod. 72 [64] C. Ramalhete, J. Molnar, S. Mulhovo, et al., New potent P-glycoprotein
(2009) 2009–2013. modulators with the cucurbitane scaffold and their synergistic interaction
[43] Z.Y. Lin, X. Liua, F. Yanga, et al., Structural characterization and identifica- with doxorubicin on resistant cancer cells, Bioorg. Med. Chem. Lett. 17
tion of five triterpenoid saponins isolated from Momordica cochinchinensis (2009) 6942–6951.
extracts by liquid chromatography/tandem mass spectrometry, Int. J. Mass [65] L. Zheng, Y.M. Zhang, Y.Z. Zhan, C.X. Liu, Momordica cochinchinensis
Spectrom. 328–329 (2012) 43–66. seed extracts suppress migration and invasion of human breast cancer ZR-
[44] J.R. Weng, L.Y. Bai, C.F. Chiu, et al., Cucurbitane triterpenoid from 75-30 cells via down-regulating MMP-2 and MMP-9, Asian Pac. J. Cancer
Momordica charantia induces apoptosis and autophagy in breast cancer Prev. 15 (2014) 1105–1110.
cells, in part, through peroxisome proliferator-activated receptor activation, [66] T. Yokozawa, H.Y. Kim, H.J. Kim, et al., Amla (Emblica officinalis Gaertn.)
Evid. Based Complement. Alternat. Med. 2013 (2013) 1–12. prevents dyslipidaemia and oxidative stress in the ageing process, Br. J.
[45] Y.W. Liao, C.R. Chen, J.L. Hsu, et al., Sterols from the stems of Momordica Nutr. 97 (2007) 1187–1195.
charantia, J. Chin. Chem. Soc. 58 (2011) 893–898. [67] P.V. Nerurkar, L.M. Johns, L.M. Buesa, et al., Momordica charantia (bitter
[46] A. Blum, C. Loerz, H.J. Martin, et al., Momordica charantia extract, a melon) attenuates high-fat diet-associated oxidative stress and neuroinflam-
herbal remedy for type 2 diabetes, contains specific 11-hydroxysteroid mation, J. Neuroinflamm. 8 (2011) 1–19.
dehydrogenase type 1 inhibitor, J. Steroid Biochem. Mol. Biol. 128 (2012) [68] Z.Y. Lin, X. Liua, F. Yanga, et al., Structural characterization and identifica-
51–55. tion of five triterpenoidsaponins isolated from Momordica cochinchinensis
[47] A.C. Keller, J. Ma, A. Kavalier, et al., Saponins from the traditional extracts by liquid chromatography/tandem mass spectrometry, Int. J. Mass
medicinal plant Momordica charantia stimulate insulin secretion in vitro, Spectrom. 328–329 (2012) 43–66.
Phytomedicine 19 (2011) 32–37. [69] A. Padmashree, G.K. Sharma, A.D. Semwal, et al., Studies on antioxy-
[48] R. Hazarika, P. Parida, B. Neog, et al., Binding Energy calculation of GSK- genic activity of bitter gourd (Momordica charantia) and its fractions using
3 protein of Human against some anti-diabetic compounds of Momordica various in vitro models, J. Sci. Food Agric. 91 (2010) 776–782.
charantia linn (Bitter melon), Bioinformation 8 (2012) 251–254. [70] H.Y. Kim, S.M. Sin, S. Lee, et al., The butanol fraction of bitter melon
[49] H.Y. Lo, T.Y. Ho, C. Lin, et al., Momordica charantia and its novel polypep- (Momordica charantia) scavenges free radicals and attenuates oxidative
tide regulate glucose homeostasis in mice via binding to insulin receptor, stress, Prev. Nutr. Food Sci. 18 (2013) 18–22.
J. Agric. Food Chem. 61 (2013) 2461–2468. [71] U.S. Akula, B. Odhav, In vitro 5-lipoxygenase inhibition of polyphenolic
[50] T. Uebanso, H. Arai, Y. Taketani, et al., Extracts of Momordica charantia antioxidants from undomesticated plants of South Africa, J. Med. Plants
suppresses postprandial hyperglycemia in rats, J. Nutr. Sci. Vitaminol. 53 Res. 2 (2008) 207–212.
(2007) 482–488. [72] H. Phan-Thi, Y. Wache, Isomerization and increase in the antioxidant prop-
[51] F. Tayyab, S.S. Lal, Antidiabetic, hypolipidemic and antioxidant activity erties of lycopene from Momordica cochinchinensis (gac) by moderate heat
of Momordica charantia on Type-II diabetic patient in Allahabad, India, treatment with UV–vis spectra as a marker, Food Chem. 156 (2014) 58–63.
Int. J. Pharm. Biol. Sci. 4 (2013) 932–940. [73] C. Myojin, N. Enami, A. Nagata, et al., Changes in the radical-scavenging
[52] M. Firdous, R. Koneri, C.H. Sarvaraidu, et al., NIDDM antidiabetic activ- activity of bitter gourd (Momordica charantia L.) during freezing and
ity of Saponins of Momordica cymbalaria in streptozotocin-nicotinamide frozen storage with or without blanching, J. Food Sci. 73 (2008)
NIDDM mice, J. Clin. Diagn. Res. 3 (2009) 1460–1465. C546–C550.
[53] V. Palanivel, M. Shafi, K.L. Senthil Kumar, Antidiabetic and hypolipidemic [74] K. Nantachit, P. Tuchinda, Antimicrobial activity of hexane and
activities of Momordica tuberosa unripe fruit extract on diabetic induced dichloromethane extracts from Momordica cochinchinensis (Lour.) spreng
rats, Int. J. Adv. Pharm. Gen. Res. 1 (2013) 33–40. leaves, Thai Pharm. Health Sci. 4 (2009) 15–20.
[54] P.S. Rao, G.K. Mohan, Beneficial effects of Momordica dioica seed extract [75] Y.X. Wang, J. Jacob, P.T. Wing field, et al., Anti-HIV and antitumor pro-
on lipid profile status in streptozotocin induced diabetic rats, Int. J. Pharm. tein MAP30, a 30 kDa single-strand type-I RIP, shares similar secondary
Sci. 2 (2014) 464–467. structure and beta sheet topology with the A chain of ricin, a type-II RIP,
[55] I. Hasan, S. Khatoon, Effect of Momordica charantia (bitter gourd) tablets Protein Sci. 9 (2009) 138–144.
in diabetes mellitus: Type 1 and Type 2, Prime Res. Med. 2 (2012) 72–74. [76] Y.S. Bot, L.O. Mgbojik, C. Nwosu, et al., Screening of the fruit pulp extract
[56] E.L. Franca, E.B. Ribeiro, E.F. Scherer, et al., Effects of Momordica cha- of Momordica balsamina for anti HIV property, Afr. J. Biotechnol. 6 (2007)
rantia L. on the blood rheological properties in diabetic patients, BioMed 47–52.
Res. Int. 2014 (2014) 1–8. [77] J.M. Adesina, L.A. Afolabi, T.I. Ofuya, Evaluation of insecticidal prop-
[57] E. Basch, S. Gabardi, C. Ubricht, Bitter melon (Momordica charantia): erties of Momordica charantia in reducing oviposition and seed damaged
a review of efficacy and safety, Am. J. Health Syst. Pharm. 60 (2003) by Callosobruchus maculates (Fab.) Walp, J. Agric. Technol. 8 (2012)
356–359. 493–499.
[58] C.J. Li, S.J. Tsang, C.H. Tsai, et al., Momordica charantia extract induces [78] M.M. Essa, P. Subramanian, Hibiscus Sabdariffa affects ammonium chlo-
apoptosis in human cancer cells through caspase- and mitochondria- ride induced hyperammonemic rats, Evid. Based Complement. Alternat.
dependent pathways, Evid. Based Complement. Alternat. Med. 2012 Med. 4 (2007) 321–325.
(2012) 1–11. [79] C.K. Lii, H.W. Chen, W.T. Yun, et al., Suppressive effects of wild bitter
[59] R. Soundararajan, P. Prabha, U. Rai, et al., Antileukemic potential of gourd (Momordica charantia Linn. var. abbreviate ser.) fruit extracts on
Momordica charantia seed extracts on human myeloid leukemic HL60 inflammatory responses in RAW 264.7 macrophages, J. Ethnopharmacol.
cells, Evid. Based Complement. Alternat. Med. 2012 (2012) 1–10. 122 (2009) 227–233.
[60] P. Pitchakarn, K. Ogawa, S. Suzuki, et al., Momordica charantia leaf extract [80] C.I. Amah, O.E. Yama, C.C. Noronha, Infecund evaluation of cycling
suppresses rat prostate cancer progression in vitro and in vivo, Cancer Sci. female Sprague-Dawley rats: an aftermath treatment with Momordica cha-
101 (2010) 2234–2240. rantia seed extract, Middle East Fertil. Soc. J. 17 (2012) 37–41.
[61] E.F. Fang, C.Z.Y. Zhang, J.H. Wong, et al., The MAP30 protein from bitter [81] O.E. Yama, F.I. Duru, Temporal adaptation in the testes of rat adminis-
gourd (Momordica charantia) seeds promotes apoptosis in liver cancer tered single dose Momordica charantia for three interrupted spermatogenic
cells in vitro and in vivo, Cancer Lett. 324 (2012) 66–74. cycles: Cytometric quantification, Middle East Fertil. Soc. J. 16 (2011)
[62] S.D. Xiong, K. Yu, X.H. Liu, et al., Ribosome-inactivating proteins iso- 194–199.
lated from dietary bitter melon induces apoptosis and inhibits histone [82] M.S. Rakh, A.N. Khedkar, N.N. Aghav, et al., Antiallergic and analgesic
deacetylase-1 selectively in premalignant and malignant prostate cancer activity of Momordica dioica Roxb. wild fruit seed, Asian Pac. J. Trop.
cells, Int. J. Cancer 125 (2009) 774–782. Med. (2012) S192–S196.
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001
+Model
FSHW-40; No. of Pages 11 ARTICLE IN PRESS
G. Nagarani et al. / Food Science and Human Wellness xxx (2014) xxx–xxx 11
[83] Z.A. Malik, M. Singh, P.L. Sharma, Neuroprotective effect of Momordica Amino Acid Requirements in Human Nutrition. Report of a Joint
charantiain global cerebral ischemia and reperfusion induced neuronal WHO/FAO/UNU Expert Consultation. WHO Technical Report Series, No.
damage in diabetic mice, J. Ethnopharmacol. 133 (2011) 729–734. 935, 2007, pp. 284.
[84] R. Horax, N. Hettiarachchy, A. Kannan, et al., Proximate composition [86] D.B. Rodriguez, L.C. Raymundo, T.C. Lee, et al., Carotenoid pigment
and amino acid and mineral contents of Mormordica charantia L. peri- changes in ripening Momordica charantia fruits, Ann. Bot. 40 (1975)
carp and seeds at different maturity stages, Food Chem. 122 (2010) 615–624.
1111–1115. [87] L.T. Vuong, A.A. Franke, L.J. Custer, et al., Momordica cochinchinensis
[85] WHO/FAO/UNU (World Health Organization/Food and Agriculture Orga- Spreng. (Gac) fruit carotenoids reevaluated, J. Food. Comp. Anal. 19 (2006)
nization of the United Nations/United Nations University), Protein and 664–668.
Please cite this article in press as: G. Nagarani, et al., Food prospects and nutraceutical attributes of Momordica species: A potential tropical
bioresources – A review, Food Sci. Hum. Wellness (2014), http://dx.doi.org/10.1016/j.fshw.2014.07.001