Pharmacognosy Magazine

: 2015  |  Volume : 11  |  Issue : 44  |  Page : 501--510

Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes

Kripa Shankar1, Sumit K Singh2, Durgesh Kumar3, Salil Varshney1, Abhishek Gupta1, Sujith Rajan3, Ankita Srivastava3, Muheeb Beg1, Anurag Kumar Srivastava4, Sanjeev Kanojiya5, Dipak K Mishra6, Anil N Gaikwad1,  
1 Division of Pharmacology, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India
2 Division of Botany, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India
3 Division of Pharmacology, CSIR Central Drug Research Institute; Academy of Scientific and Innovative Research, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India
4 Division of Toxicology, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India
5 Sophisticated Analytical Instrument Facility, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India
6 Division of Botany, CSIR Central Drug Research Institute; Division of Pharmacology, CSIR Central Drug Research Institute, Lucknow, Uttar Pradesh, India

Correspondence Address:
Anil N Gaikwad
BS 10/1, Sector 10, PCN 208, Division of Pharmacology, CSIR- Central Drug Research Institute, Jankipuram Extension, Lucknow 226 031, Uttar Pradesh


Background: Cucumis melo ssp. agrestis var. agrestis (CMA) is a wild variety of C. melo. This study aimed to explore anti-dyslipidemic and anti-adipogenic potential of CMA. Materials and Methods: For initial anti-dyslipidemic and antihyperglycemic potential of CMA fruit extract (CMFE), male Syrian golden hamsters were fed a chow or high-fat diet with or without CMFE (100 mg/kg). Further, we did fractionation of this CMFE into two fractions namely; CMA water fraction (CMWF) and CMA hexane fraction (CMHF). Phytochemical screening was done with liquid chromatography-mass spectrometry LC- (MS)/MS and direct analysis in real time-MS to detect active compounds in the fractions. Further, high-fat diet fed dyslipidemic hamsters were treated with CMWF and CMHF at 50 mg/kg for 7 days. Results: Oral administration of CMFE and both fractions (CMWF and CMHF) reduced the total cholesterol, triglycerides, low‐density lipoprotein cholesterol, and very low‐density lipoprotein-cholesterol levels in high fat diet-fed dyslipidemic hamsters. CMHF also modulated expression of genes involved in lipogenesis, lipid metabolism, and reverse cholesterol transport. Standard biochemical diagnostic tests suggested that neither of fractions causes any toxicity to hamster liver or kidneys. CMFE and CMHF also decreased oil-red-O accumulation in 3T3-L1 adipocytes. Conclusion: Based on these results, it is concluded that CMA possesses anti-dyslipidemic and anti-hyperglycemic activity along with the anti-adipogenic activity.

How to cite this article:
Shankar K, Singh SK, Kumar D, Varshney S, Gupta A, Rajan S, Srivastava A, Beg M, Srivastava AK, Kanojiya S, Mishra DK, Gaikwad AN. Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes .Phcog Mag 2015;11:501-510

How to cite this URL:
Shankar K, Singh SK, Kumar D, Varshney S, Gupta A, Rajan S, Srivastava A, Beg M, Srivastava AK, Kanojiya S, Mishra DK, Gaikwad AN. Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes . Phcog Mag [serial online] 2015 [cited 2020 Jan 20 ];11:501-510
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The oral administration of Cucumis melo agrestis fruit extract (CMFE) and its fractions (CMWF and CMHF) improved serum lipid profile in HFD fed dyslipidemic hamsters.CMFE, CMWF and CMHF significantly attenuated body weight gain and eWAT hypertrophy.The CMHF decreased lipogenesis in both liver and adipose tissue.CMFE and CMHF also inhibited adipogenesis in 3T3-L1 adipocytes.


Abbreviation used: CMA: Cucumis melo ssp. agrestis var. agrestis, CMFE: CMA fruit extract, CMWF: CMA water fraction, CMHF: CMA hexane fraction, FAS: Fatty acid synthase, SREBP1c: Sterol regulatory element binding protein 1c, ACC: Acetyl CoA carboxylase, LXR a: Liver X receptor α.


Dyslipidemia is a lipoprotein metabolism disorder that displays increased cholesterol, triglyceride (TG) and low-density lipoprotein-cholesterol (LDL-c) along with decreased high-density lipoprotein-cholesterol (HDL-c) in blood. [1],[2] Dyslipidemia is a major risk factor attributed to the development of cardiovascular diseases (CVDs). According to World Health Organization, CVDs are the number one cause of deaths worldwide. Therefore, it is a prime consideration for treatment of dyslipidemia to reduce elevated levels of lipid profile, i.e. TGs, total cholesterol (TC), and LDL-c along with an increase in HDL-c. Treatment options for these disorders include diet interventions, physical exercise, surgery, and medication. The anti-dyslipidemic drugs that are currently available in the market include statins, fibrates, niacin, ezetimibe, and bile acid binding resins. [3],[4] However, a small but clinically significant population taking these medications experience adverse effects. Statins are known to increase hepatic enzymes and muscle toxicity. [5],[6] Likewise, long-term therapy of fibrate in patients causes supersaturation of gallbladder bile, which increases the incidence of cholesterol gallstones. [7] Exploration of medicinal plants has always been an immense source of drugs and majority of the currently available drugs have been derived directly or indirectly from them. These days herbal drugs are being prescribed widely due to their effectiveness with minimum side effects and relatively low cost. The World Health Organization also considers medicinal plants as alternatives in the treatment of various diseases and the focus of research professionals for plants is increasing day by day. [8]

Cucumis melo ssp. agrestis var. agrestis (CMA) (Naudin) Pangalo var. agrestis Naudin, commonly known as wild melon (in English) or kachari (in Hindi) under the family cucurbitaceae. [9] CMA is a common climbing or prostrate herb, distributed almost throughout India and neighboring countries. The fruits of this plant possess the stomachic property and are also used to treat burns and abrasions. Seeds have antitussive, antioxidant, digestive, febrifuge and vermifuge properties, and seed oil extract was reported for anti-fungal activity. [10],[11] Recently, we have observed that flavonoids have co-existing anti-dyslipidemic and anti-adipogenic activity, although both activities are distinct. [12] Furthermore, anti-adipogenic activity has also been reported for some of the statin classes of compound. [13],[14] Syrian golden hamsters have been demonstrated as a valuable model of high fat diet (HFD) induced dyslipidemia, and it is well-suited for screening of anti-dyslipidemic agents. [12],[15] In addition, hamsters also have a similarity to human plasma lipid distribution, synthesis, and excretion. [16],[17] Our present study aimed to explore the anti-dyslipidemic and anti-adipogenic potential of fruit extract (excluding seed) and fractions of this plant in HFD-fed dyslipidemic hamsters. The anti-dyslipidemic activity was further assessed by gene expression and protein immunoblotting analysis in liver and adipose tissue.

 Materials And Methods

Plant materials

Ripe fruits of CMA were collected from our institute campus at Lucknow, India in July 2013. The herbarium specimen of this plant with voucher specimen number DKM24778 has been deposited in the medicinal plant herbarium of Council of Scientific and Industrial Research (CSIR)-Central Drug Research Institute (CDRI).


High-fat diet (Cat No. 12451) was purchased from Research Diets Inc., USA. Fenofibrate, used as positive control was purchased from Sigma-Aldrich, USA. Ethyl alcohol was procured from Merck, Germany and hexane from CDH, New Delhi, India. (4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay (MTT) and oil-red-O powder were purchased from Sigma. The kits for the assay of blood glucose, TC, TG, HDL-c, LDL-cholesterol, alanine aminotransferase (ALT), aspartate aminotransferase (AST), and creatinine were purchased from Merck Specialities Pvt., Ltd., fatty acid synthase (FAS), acetyl CoA carboxylase (ACC), and ATP-citrate lyase antibodies were purchased from Cell Signaling Technology, Inc., (Beverly, MA, USA).

Extraction and fractionation

The fruits of this plant were collected, washed, and oven dried at a constant temperature of 37°C after removal of seeds. Thereafter, these were made into fine powder using a grinder and kept in an airtight amber color container protected from light. The 130 g powder was extracted in ethanol for 24 h on a mechanical shaker at room temperature. The solvent was filtered off, and the residue was macerated again with 500 ml fresh solvent consecutively 2 times for next 2 days. Finally, the residue was discarded and all the filtrates were clubbed and concentrated under reduced pressure on a rotary evaporator (BUCHI, Switzerland) at 40°C. Finally, 7 g of the crude ethanolic extract obtained and partitioning into 1:1 hexane: Water mixture. The fractions resulted in 3.29 (hexane) and 1.68 g (water) residue after solvent evaporation. Both the fractions were kept in air tight glass containers away from light and subjected to further study.

Liquid chromatography-mass kept in air tight glass containers away from light and subjected to further study LC-MS/MS analysis

The liquid chromatography-mass spectrometry (LC-MS) and LC-MS/MS analysis of fruit extract's fractions (excluding seed) of CMA was performed on waters tandem quadrupole detector triple quadrupole MS (USA). It was equipped with waters, H-Class acquity ultra performance LC (UPLC) system, and electrospray ionization (ESI) source. The column was used thermo accucore AQ C18 100 × 3 mm, 2.6 mm, and dual mode (+) LC-ESI-MS experiments were performed. 5 ml of the sample was injected through auto-sampler into UPLC flow. For the separation of individual compounds, the mobile phase used (a) methanol and acetonitrile (50:50) and (b) 5 mm ammonium acetate in 95% water. A linear gradient elution was performed at the flow rate of 0.250 ml/min as 80-40% B in 0-5 min; 40% B in 5-6 min; 20% B in 7-8 min. Nitrogen was used as the nebulizing and drying gas at flow rates of 30 and 650 L/h, respectively. The ESI source potentials were capillary voltage 3.5 kV; cone potential at 30 V for every experiment. The Source and desolvation temperature was at 120 and 350°C, respectively. The mass resolution was set approximately 1000 and the mass analyzer was scanned between 150 Th and 750 Th in 0.5 s. Online tandem mass spectra of various ions were measured by precursor ion selection in MS 1 followed by collision induced dissociation and analysis of the daughter ions by MS 2 . Argon was used as collision gas and optimized at a pressure to achieve 5-10% transmission of the precursor ion. The collision energy was ramped between 10 eV and 15 eV to achieve significant fragmentation. Data acquisition and processing were carried out using MassLynx V4.1 software change note 714 software (Waters Corporation, 34 Maple Street, Milford, MA ,01757). The spectra were accumulated from the top of extracted ion chromatogram peak.

Direct analysis in real time-mass spectrometry

The direct analysis in real time (DART)-MS was recorded on a JEOL-AccuTOF JMS-T100LC MS having a DART source. The samples were subjected as such in front of DART source. Dry helium gas was used for ionization at 4 L/min flow rate and source temperature kept at 350°C. The orifice 1 was set at 28 V and spectra collected as an average of 6-8 scan.

Differentiation of 3T3-L1 adipocytes

The 3T3-L1 cell line was purchased from the American type culture collection. Cells were cultured in a humidified atmosphere at 37°C and 5% CO 2 in DMEM containing 10% (v/v) heat-inactivated fetal bovine serum and penicillin-streptomycin antibiotics (cDMEM). For adipogenic induction, cells were seeded in 24 well-plates. Two days postconfluence, culture medium was replaced with differentiation medium [medium containing insulin 5 mg/ml, 3-isobutyl-1-methylxanthine 0.5 mM, and dexamethasone 250 nM (MDI)]. This medium was replaced after 48 h with medium containing 5 mg/ml insulin. This medium was replaced after 72 h, and cells were maintained in cDMEM. Lipid droplets started appearing from day 4, and > 90% of cells showed lipid globules 6-8 days after induction.

MTT assay

MTT assay was performed as described previously [12] and absorbance was measured at 570 nm using ELISA plate reader (BioTek, USA).

Animals and diet

Dyslipidemia was induced in 8 week old, (100-120 g body weight) Syrian golden hamsters (Mesocricetus auratus) by feeding a high-fat diet (Research Diets Inc., Cat. No: D12451, 45% kCal). Hamsters used in the study were taken from the colony of the Laboratory Animal Division, CSIR-CDRI and were kept in controlled laboratory conditions of temperature (23 ± 2°C), relative humidity (50-60%), and light (300 Lx at floor level, 12/12 h light/dark cycle). All experimental procedures adopted in this study were previously approved by the Institutional Animal Ethics Committee in accordance with the guidelines of the Committee for the Purpose of Control and Supervision of Experiments on Animals formed by the government of India. Standard pellet food and high-fat diet (Research Diets Inc., 12451), kept at 4°C was administered daily (80 g diet/cage) at a fixed time in the morning. The leftover diet of the previous day was weighed for the net food intake before being discarded. All groups were having free access to diet and water.

Experimental design for anti-dyslipidemic and anti-hyperglycemic activity of Cucumis melo ssp. agrestis var. agrestis fruit extract, Cucumis melo ssp. agrestis var. agrestis water fraction and Cucumis melo ssp. agrestis var. agrestis hexane fraction

The animals with identification marks were acclimatized for 7 days before the experiment. The control group of hamster was fed with normal chow diet. High-fat diet (45% kcal HFD, day 1-day 10) were given in all other groups, i.e. Vehicle, fenofibrate, CMA fruit extract (CMFE), CMA water fraction (CMWF), and CMA hexane fraction (CMHF). All groups were having free access to diet and water. Likewise, the body weight of the animals was recorded daily before feeding and drug administration. Fenofibrate, CMFE or CMA water fraction (CMWF), and CMA hexane fraction (CMHF) were suspended in the 0.1% gum acacia solution and gavaged orally, once daily at a fixed time for seven consecutive days (day 4-10) to treated groups and vehicle to the parallel control. The same experimental procedure was followed for assessment of anti-dyslipidemic activity of CMWF and CMHF.

Blood collection, serum analysis, and histological analysis

The blood withdrawn from the retro-orbital plexus of anesthetized animals was collected in micro-centrifuge tubes and serum was separated by centrifugation. TG, TC, HDL-c, LDL-cholesterol, glucose, ALT, AST, and creatinine were estimated using Merck selectra junior bio-analyzer (Merck Millipore). Very low‐density lipoprotein-cholesterol (VLDL-c) was calculated using the formula (TG/5) of Friedewald. The sections of epididymal white adipose tissue (eWAT) and liver were fixed in 10% formalin, dehydrated, and embedded in paraffin. Further, eWAT and liver sections were stained with hematoxylin and eosin to examine the morphology.

Real time polymerase chain reaction

Total RNA was isolated from liver and eWAT using TRIZOL reagent (Invitrogen, CA, USA). First strand cDNA synthesis was performed using high-capacity cDNA reverse transcription Kit (Applied Biosystems™) and subsequently used for quantitative real time polymerase chain reaction (PCR) analysis on Light Cycler 480 (Roche Diagnostics). Statistical analysis of the quantitative real time PCR was obtained using the (2 -ΔΔCt) method, which calculates the relative changes in gene expression of the target, normalized to an endogenous reference (18S rRNA) and relative to a calibrator that serves as a control group. Gene-specific primer pairs used in these studies are listed in [Table 1].{Table 1}

Western blotting

Liver and eWAT were freeze-thawed and triturated in liquid nitrogen and protein were isolated using mammalian cell lysis buffer supplemented with 100 mm EDTA, protease inhibitor, and phosphatase inhibitor (Sigma-Aldrich). Protein concentration was determined using the bicin-choninic acid method (Sigma) and further western blotting procedure was done as described previously. [18] To validate equal loading, actin was used as an internal loading control.

Statistical analysis

For in vivo studies, data were expressed as a mean + standard error of mean. Comparisons between the treatment groups and control were performed by one-way analysis of variance followed by Bonferroni's multiple comparison test. For in vitro studies, data were expressed as mean + standard deviation. Comparisons between the treatment groups and control were performed using Student's t-test. A probability value of P < 0.05 (*), 0.01 (**) and 0.001 (***) was used as a measure of statistical significance. Data were analyzed on Graph Pad Prism (Version 5.00, Graph Pad Software Inc., San Diego, CA, USA).


Cucumis melo ssp. agrestis var. agrestis fruit extract attenuates dyslipidemia and improves hyperglycemia

CMFE treatment in HFD-fed dyslipidemic hamster reduced increase in TC, LDL-c, however, we could not get any difference in TG [Figure 1]a, b and d. HFD induced hyperglycemia was also improved with treatment of CMFE [Figure 1]c. In addition, HDL-c and HDL-c to TC ratio were also improved when treated with CMFE [Figure 1]e and f. Furthermore, we examined the intracellular toxicity of CMFE in 3T3-L1 adipocytes, using the MTT assay. The result of MTT assay proves that CMA treatment is safe [Figure 1]g. Different concentrations of CMFE (25, 50, 100 mg/ml) were supplemented with MDI during differentiation. The absorbance of extracted ORO accumulated in lipid droplets shows that CMA significantly inhibits adipogenesis [Figure 1]h.{Figure 1}

Phytochemical screening

The bioactive fractions of CMA were investigated by LC-MS/MS. The previously reported data of Cucumis species showed the presence of carbohydrates, glycosides, phenolics, and flavonoids. [19] Similarly, the nonpolar oily fraction contains fatty acids like 16-Octadecenoic acid, methyl ester, estra-1, 3, 5 (10)-trien-17-beta-ol, hexadecanoic acid, 2-hydroxy ethyl ester, etc. [20] Our preliminary study and MS data also suggested the presence of carbohydrates, phenolics, and their glycosides. The compound eluted at 1.5 min having molecular weight 342 Da, was highly abundant in the aqueous fraction. The MS/MS spectra indicated that the molecule contains a sugar moiety (−162 Da) with the 180 Da unit. Thus, it could be expected as disaccharides sugar. Similarly, most of the compounds eluted subsequently shown a characteristic loss of −162 Da from parent ion that suggested the loss of a hexose unit. While the presence of indicative ion at m/z 91, 105, 107, 135 in MS/MS spectra designates the phenolic structure, and these compounds were identified as phenolic glycosides. Apart from this, compound eluted at 9.09 showed subsequent loss of the CH 2 unit with the losses of H 2 O and CH 3 OH. It suggested the presence of long carbon chain with the -OH and -O-CH 3 functional group. The chromatographic and MS data of detected metabolites are shown in [Table 2]. However, the whole metabolites detection was not possible only from ESI source. Thus, the metabolites fingerprint of both the fraction CMWF and CMHF were recorded on DART-MS and shown in [Figure 2]a. This MS can be recognized as fingerprints to discriminate the fractions metabolite and for future reference.{Table 2}

Cucumis melo ssp. agrestis var. agrestis fractions suppress high-fat diet-induced weight gain, improves dyslipidemia and hyperglycemia

The body weight of the HFD fed group significantly increased while CMWF and CMHF treatment significantly attenuated gain in body weight starting from 7 th day to the end of the experimental period without any change in food intake throughout the experimental period [Figure 2]b and c. HFD significantly increased TC (4.1 fold), TG (2.2 fold), LDL-c (5.8 fold), VLDL-c (2.2 fold) in Syrian golden hamsters, which were decreased [TC (28.8, 41.2, and 36.9%), TG (29.3, 30.2, 38.3%), LDL-c (34.9, 31.8, 54.7%) with increased HDL-c (41.4, 30.5, 37.6%)] in serum, respectively by fenofibrate (100 mg/kg), CMWF, and CMHF (50 mg/kg) treated animals [Figure 2]d-h. Our result showed that the dyslipidemic hamsters exhibited a profound decrease in the HDL-c/TC ratio, an atherogenic marker [Figure 2]i. This atherogenicity is considered to be combined with dyslipidemia. [21] Animals fed with HFD for 11 days lead to increased serum glucose compared with chow-fed animals. CMA fractions treatment significantly suppressed the elevation of serum glucose in HFD fed hamsters [Figure 2]j.{Figure 2}

Cucumis melo ssp. agrestis var. agrestis fractions reduced adipose hypertrohy and hepatic lipid accumulation in vivo in Syrian golden hamsters without any toxicity

To investigate whether CMA decreases adiposity, hamsters were sacrificed and eWAT removed and weighed. The weight of eWAT was increased in the HFD-fed hamsters compared to the chow-fed hamsters, and was significantly decreased by the administration of Fenofibrate, CMWF, and CMHF [Figure 3]a and b. HFD- fed hamster showed adipocyte hypertrophy, while the adipocyte phenotype of CMA fractions (CMWF and CMHF) treated group was similar to chow diet fed animals. In addition to this, the liver histological sections of CMA fractions (CMWF and CMHF) treated animals also showed decrease hepatic lipid accumulation [Figure 3]c. The levels of AST, ALT, and creatinine that indicates liver and kidney injury, were significantly improved in CMA fractions treated animals [Figure 3]d-f.In addition, the CMA treated hamsters did not induce any significant changes in the weight of liver (data not shown). Thus, the data indicate that administration of 50 mg/kg/day of CMA fractions for 7 days induced no biochemically detectable adverse toxic effects in the hamsters.

Cucumis melo ssp. agrestis var. agrestis fractions inhibited adipogenesis and lipogenesis, increased lipid metabolism and reverse cholesterol transport

Different concentrations of both CMA fractions (CMWF and CMHF at 25, 50, 100 mg/ml) were supplemented with MDI during differentiation of 3T3- l1 adipocytes. The absorbance of extracted ORO accumulated in lipid droplets shows that CMHF significantly inhibits adipogenesis [Figure 4]a. Further, FAS protein level was also reduced more prominently in CMHF treated eWAT [Figure 4]b. CMWF and CMHF treatment also decreased FAS, and ACC in the liver. Hepatic ATP citrate-lyase was reduced significantly when treated with CMHF. However, we could not get any significant change in ATP-citrate lyase protein expression when treated with CMWF [Figure 4]c. Hence, we further analyzed the mRNA expression of genes involved in lipogenesis, lipid metabolism, and reverse cholesterol transport only in CMHF treated animals. The CMHF treatment increased hepatic mRNA expression of liver X receptor a (LXR a), LPL and significantly decreased expression of sterol regulatory element binding protein 1c (SREBP1c) [Figure 4]d-f. Further, hepatic mRNA expression of lecithin-cholesterol acyltransferase (LCAT) and apolipoprotein A-I (APOA1), involved in reverse cholesterol transport were significantly enhanced by treatment of CMHF [Figure 4]g and h.{Figure 3}{Figure 4}


Traditionally, India has very long history of using natural extracts in the form of Ayurvedic medicines. Currently, people throughout the world are recognizing the value of natural compounds. [22],[23] CMA var. agrestis is a wild variety of C. melo and known as wild melon or musk melon. C. melo var. agrestis, being wild variety is economically cheaper and present in enormous quantity comparing with its original variety C. melo. The plants of Cucurbitaceae family had been widely used in treatments of many diseases. [24],[25],[26] The previous studies have reported the presence of alkaloids, flavonoid, terpenoids, and phenolic compounds in seed extract of C. melo. [11] However, to the best of our knowledge, anti-dyslipidemic activity of CMA has not been explored until date. The purpose of the present study was to assess the anti-dyslipidemic activity of CMA extract and its subsequent fractions and further evaluation of its anti-adipogenic activity. In our study, results show that CMFE attenuates dyslipidemia and improves hyperglycemia that lead us to do fractionization of this extract and further assessment of anti-dyslipidemic activity of both fractions (CMWF and CMHF). Both fractions showed significantly decreased serum lipid and glucose level in our primary assays. Many natural compounds have been previously studied in great detail for their potential to inhibit adipogenesis and/or lipid accumulation capacities such as in some noted cases of berberine, hesperidin, naringin, curcumin. [14],[27],[28],[29],[30],[31] Our recent study also showed that the anti-adipogenic compounds also show anti-dyslipidemic activities. Hence further, we performed an anti-adipogenic activity of CMFE in 3T3-L1 adipocytes and found that CMFE decreases concentration-dependent oil-red-O accumulation, a dye used for staining of neutral TGs and lipids which indicates that CMFE causes decrease in lipid accumulation during 3T3-L1 adipogenic differentiation. Based on the data presented in this study, CMA fractions (CMWF and CMHF) treatment significantly improved serum dyslipidemia by decreasing TG, TC, and LDL-c with increase in HDL-c, and the ratio of HDL-c to TC. Diabetic dyslipidemia is a complex cluster of abnormalities. [2] In addition to the hypolipidemic effects, CMWF and CMHF treatment also showed hypoglycemic activity in dyslipidemic hamsters. Treatment of CMA fractions also attenuated body weight and eWAT weight, a marker of obesity. Histological analysis also proved that CMA fractions decreased the hypertrophy in adipocyte, a marker of dysfunctional adipose tissue. Moreover, hepatic lipid accumulation a marker of hepatic insulin resistance is also reduced with treatment of CMWF and CMHF. [32],[33] Hence taken together, CMA fractions attenuated body weight gain, ameliorated dyslipidemia, and hyperglycemia in HFD fed dyslipidemic hamsters. FAS is a very well-known lipogenic target for SREBP-1c, which was significantly decreased when treated with CMWF and CMHF in eWAT as well as in the liver, further contributing to the effect of CMA fractions on modulating circulating lipids. CMWF and CMHF treatment also decreased the protein expression of ACC. Hepatic ATP - citrate lyase was decreased when treated with CMHF, but we could not get any significant difference in ATP- citrate lyase with CMWF treatment. We could not get any significant changes in adipogenesis and other markers (e.g. ATP-citrate lyase) with CMWF. Thus, further mRNA expression analysis was performed with CMHF only. LXR a is a sensor of cholesterol excess and its activation in dyslipidemic hamsters led to an increase in reverse cholesterol transport and reduced lipid accumulation. [34] In this study, CMHF treatment in HFD-fed hamsters increased the hepatic mRNA expression of LXR a. Further, SREBP-1c is considered as a central mediator of obesity and insulin resistance and master regulator of ATP-citrate lyase, ACC, and FAS. ATP-citrate lyase is a lipogenic enzyme that converts citrate to acetyl-coenzyme A. Acetyl-coenzyme A is further converted to malonyl-CoA. Malonyl-CoA is known to play a key role for chain elongation in fatty acid biosynthesis. [35] Liver-specific ATP-citrate lyase downregulation via adenovirus-mediated RNA interference has been reported to reduce expression of peroxisome proliferator-activated receptor-gamma and the entire lipogenic program in the liver. [36] Hence, we hypothesize that CMWF and CMHF increase expression of LXR a and inhibits expression of the transcription factor SREBP1c, leading to a reduced expression of its all major targets including FAS, ACC, and ATP-citrate lyase to inhibit lipogenesis in the liver as well as in adipose tissue. Overexpression of APOA-I limits progression and reduces pre-existing atherosclerosis hence, increasing the levels of APOA1 A-I has been a therapeutic target in CVDs. [37],[38] CMHF treatment increased the mRNA expression of APOA1 and LCAT, the genes involved in reverse cholesterol transport, proving that CMHF not only decreases lipogenesis but also increases reverse cholesterol transport. Hence, it is concluded that apart from adipose tissue, the liver is also an important player for in vivo activity of CMA. Hypertriglyceridemia (>150 mg/dL) is a common lipid abnormality associated with several other metabolic disorders. [39],[40] LPL plays an important role by catalyzing first reaction in TG metabolism and increase in LPL causes a reduction in hypertriglyceridemia. [41] Our results show that CMHF increased lipoprotein lipase mRNA expression in the liver that might be a reason for the decrease in serum TG level.


The administration of CMFE, CMWF, and CMHF significantly attenuated body weight gain and eWAT hypertrophy and improved serum TC, TG, and LDL-c levels in HFD-induced dyslipidemic hamsters. CMFE and CMHF inhibited adipogenesis in 3T3-L1 adipocytes. The dyslipidemic effects of CMHF altered the expression of LXR a, SREBP1c in the liver, and FAS in both liver and adipose tissue. These results suggest that CMA treatment is useful for treating metabolic diseases such as obesity and hyperlipidemia. Our study shows the effects of CMWF and CMHF on TC, TGs, and LDL-c along with an analysis of liver and kidney adverse reactions indicates that CMA could be a cheap, efficient, and safe lipid-lowering drug in metabolic syndrome patients.


KS, SR and AG are supported by senior research fellowship of University Grant Commission, New Delhi. SV is supported by BSC0102. DK and AS are supported by Senior Research Fellowship and Senior Research Fellowship respectively from Council of Scientific and Industrial Research. The authors acknowledge Sophisticated Analytical Instrument facility (SAIF), CSIR-CDRI for mass spectrometry analysis. The manuscript bears CDRI communication number 9113.

Financial support and sponsorship

Research work is supported by CSIR --CDRI Network projects {Projects No: BSC0102 and BSC 0106}.

Conflicts of interest

The authors declare no conflicts of interest.


1Marsh JB. Lipoprotein metabolism in obesity and diabetes: Insights from stable isotope kinetic studies in humans. Nutr Rev 2003;61:363-75.
2Mooradian AD. Dyslipidemia in type 2 diabetes mellitus. Nat Clin Pract Endocrinol Metab 2009;5:150-9.
3Ling H, Burns TL, Hilleman DE. Novel strategies for managing dyslipidemia: Treatment beyond statins. Postgrad Med 2012;124:43-54.
4Jellinger PS, Smith DA, Mehta AE, Ganda O, Handelsman Y, Rodbard HW, et al. American association of clinical endocrinologists' guidelines for management of dyslipidemia and prevention of atherosclerosis. Endocr Pract 2012;18 Suppl 1:1-78.
5Tomlinson B, Chan P, Lan W. How well tolerated are lipid-lowering drugs? Drugs Aging 2001;18:665-83.
6Armitage J. The safety of statins in clinical practice. Lancet 2007;370:1781-90.
7Caroli-Bosc FX, Le Gall P, Pugliese P, Delabre B, Caroli-Bosc C, Demarquay JF, et al. Role of fibrates and HMG-CoA reductase inhibitors in gallstone formation: Epidemiological study in an unselected population. Dig Dis Sci 2001;46:540-4.
8The WHO Traditional Medicine (TM) Strategy. 2014-2023.
9Sebastian P, Schaefer H, Telford IR, Renner SS. Cucumber (Cucumis sativus) and melon (C. melo) have numerous wild relatives in Asia and Australia, and the sister species of melon is from Australia. Proc Natl Acad Sci U S A 2010;107:14269-73.
10Adekunle AA, Oluwo OA.The nutritive value of Cucumis melo var. agrestis Scrad (Cucurbitaceae) seeds and oil in Nigeria. Am J Food Technol 2008;3:141-6.
11Kaur M, Arora R. Antioxidant activity of Cucumis melo var. agrestis seeds for their therapeutic potential. Int J Res Ayurveda Pharm 2011;2:1235-8.
12Varshney S, Shankar K, Beg M, Balaramnavar VM, Mishra SK, Jagdale P, et al. Rohitukine inhibits in vitro adipogenesis arresting mitotic clonal expansion and improves dyslipidemia in vivo. J Lipid Res 2014;55:1019-32.
13Nakata M, Nagasaka S, Kusaka I, Matsuoka H, Ishibashi S, Yada T. Effects of statins on the adipocyte maturation and expression of glucose transporter 4 (SLC2A4): Implications in glycaemic control. Diabetologia 2006;49:1881-92.
14Nicholson AC, Hajjar DP, Zhou X, He W, Gotto AM Jr, Han J. Anti-adipogenic action of pitavastatin occurs through the coordinate regulation of PPARgamma and Pref-1 expression. Br J Pharmacol 2007;151:807-15.
15Bhatia G, Rizvi F, Saxena R, Puri A, Khanna AK, Chander R, et al. In vivo model for dyslipidemia with diabetes mellitus in hamster. Indian J Exp Biol 2003;41:1456-9.
16Singh V, Tiwari RL, Dikshit M, Barthwal MK. Models to study atherosclerosis: A mechanistic insight. Curr Vasc Pharmacol 2009;7:75-109.
17Zhang Z, Wang H, Jiao R, Peng C, Wong YM, Yeung VS, et al. Choosing hamsters but not rats as a model for studying plasma cholesterol-lowering activity of functional foods. Mol Nutr Food Res 2009;53:921-30.
18Beg M, Shankar K, Varshney S, Rajan S, Singh SP, Jagdale P, et al. A clerodane diterpene inhibit adipogenesis by cell cycle arrest and ameliorate obesity in C57BL/6 mice. Mol Cell Endocrinol 2015;399:373-85.
19Ahmad MI, Ansari SH, Naquvi KJ, Shuaib M. Pharmacognostical studies and establishment of quality parameters of Cucmis melo L. CV. Namdhari. Int J Pharm Pharm Sci 2012;4:324-9.
20Sasi 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). Int J Pharmacogn Phytochem Res 2015;6:936-41.
21Hodis HN. Triglyceride-rich lipoprotein remnant particles and risk of atherosclerosis. Circulation 1999 8;99:2852-4.
22Parab RS, Mengi SA. Hypolipidemic activity of Acorus calamus L. in rats. Fitoterapia 2002;73:451-5.
23Liu Q, Kim SH, Kim SB, Jo YH, Kim ES, Hwang BY, et al. Anti-obesity effect of (8-E)-niizhenide, a secoiridoid from Ligustrum lucidum, in high-fat diet-induced obese mice. Nat Prod Commun 2014;9:1399-401.
24Teugwa CM, Boudjeko T, Tchinda BT, Mejiato PC, Zofou D. Anti-hyperglycaemic globulins from selected Cucurbitaceae seeds used as antidiabetic medicinal plants in Africa. BMC Complement Altern Med 2013;13:63.
25Fernandes NP, Lagishetty CV, Panda VS, Naik SR. An experimental evaluation of the antidiabetic and antilipidemic properties of a standardized Momordica charantia fruit extract. BMC Complement Altern Med 2007;7:29.
26Folador P, Cazarolli LH, Gazola AC, Reginatto FH, Schenkel EP, Silva FR. Potential insulin secretagogue effects of isovitexin and swertisin isolated from Wilbrandia ebracteata roots in non-diabetic rats. Fitoterapia 2010;81:1180-7.
27Huang C, Zhang Y, Gong Z, Sheng X, Li Z, Zhang W, et al. Berberine inhibits 3T3-L1 adipocyte differentiation through the PPARgamma pathway. Biochem Biophys Res Commun 2006;348:571-8.
28Kong W, Wei J, Abidi P, Lin M, Inaba S, Li C, et al. Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. Nat Med 2004;10:1344-51.
29Kim CY, Le TT, Chen C, Cheng JX, Kim KH. Curcumin inhibits adipocyte differentiation through modulation of mitotic clonal expansion. J Nutr Biochem 2011;22:910-20.
30Jang EM, Choi MS, Jung UJ, Kim MJ, Kim HJ, Jeon SM, et al. Beneficial effects of curcumin on hyperlipidemia and insulin resistance in high-fat-fed hamsters. Metabolism 2008;57:1576-83.
31Jeong SM, Kang MJ, Choi HN, Kim JH, Kim JI. Quercetin ameliorates hyperglycemia and dyslipidemia and improves antioxidant status in type 2 diabetic db/db mice. Nutr Res Pract 2012;6:201-7.
32McGarry JD. What if Minkowski had been ageusic? An alternative angle on diabetes. Science 1992;258:766-70.
33Nagle CA, Klett EL, Coleman RA. Hepatic triacylglycerol accumulation and insulin resistance. J Lipid Res 2009;50 Suppl: S74-9.
34Zhang Y, Breevoort SR, Angdisen J, Fu M, Schmidt DR, Holmstrom SR, et al. Liver LXRalpha expression is crucial for whole body cholesterol homeostasis and reverse cholesterol transport in mice. J Clin Invest 2012;122:1688-99.
35Srere PA. The citrate cleavage enzyme. I. Distribution and purification. J Biol Chem 1959;234:2544-7.
36Wang Q, Jiang L, Wang J, Li S, Yu Y, You J, et al. Abrogation of hepatic ATP-citrate lyase protects against fatty liver and ameliorates hyperglycemia in leptin receptor-deficient mice. Hepatology 2009;49:1166-75.
37Bailey D, Jahagirdar R, Gordon A, Hafiane A, Campbell S, Chatur S, et al. RVX-208: A small molecule that increases apolipoprotein A-I and high-density lipoprotein cholesterol in vitro and in vivo. J Am Coll Cardiol 2010;55:2580-9.
38Nicholls SJ, Gordon A, Johannson J, Ballantyne CM, Barter PJ, Brewer HB, et al. ApoA-I induction as a potential cardioprotective strategy: Rationale for the SUSTAIN and ASSURE studies. Cardiovasc Drugs Ther 2012;26:181-7.
39Austin MA, Hokanson JE, Edwards KL. Hypertriglyceridemia as a cardiovascular risk factor. Am J Cardiol 1998 26;81:7B-12B.
40Consensus conference: Treatment of hypertriglyceridemia. JAMA 1984;251:1196-200.
41Noh HL, Okajima K, Molkentin JD, Homma S, Goldberg IJ. Acute lipoprotein lipase deletion in adult mice leads to dyslipidemia and cardiac dysfunction. Am J Physiol Endocrinol Metab 2006;291:E755-60.