The Protective Role of Momordica charantia Fruit Extract on Diet-Induced Hypercholesterolemia in Rabbits

Research Article

The Protective Role of Momordica charantia Fruit Extract on Diet-Induced Hypercholesterolemia in Rabbits

  • Sethi J 1*
  • Kiran Dahiya K 2

*Corresponding Author: Sethi J, Department of Physiology, Pt. BD Sharma PGIMS, Rohtak, Haryana, India

Citation: Sethi J, Kiran Dahiya K. The Protective Role of Momordica charantia Fruit Extract on Diet-Induced Hypercholesterolemia in Rabbit. J Clinical Research and Reports, 3(5); DOI:10.31579/2690-1919/054

Copyright: © 2020 Sethi J. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: 19 February 2020 | Accepted: 12 March 2020 | Published: 16 March 2020

Keywords: momordica charantia; high-fat diet; thiobarbituric acid-reactive substance; atherogenic index; coronary heart diseases

Abstract

Background:  Dyslipidemia is a prominent and modifiable risk factor for the development of atherosclerosis.  This study was carried out to investigate the anti-atherogenic antioxidant potential of Momordica charantia (MC) Fruit Extract in hypercholesterolemic rabbits.  Albino rabbits (1.5-2.5 kg) of either sex were divided into four groups of six each, depending on the diet.  Group I received the standard chow diet; group II received aqueous MC fruit extract (100 mg/kg, p.o.); group III rabbits received HFD; and group IV rabbits received high fat diet (HFD) supplemented with aqueous MC fruit extract (100 mg/kg).  Blood samples were collected from the marginal vein of pinna of overnight fasted rabbits at the end of experimental period for estimation of total cholesterol (TC), triglyceride (TG) and high density lipoprotein cholesterol (HDL-C), Malondialdehyde (MDA), reduced glutathione (GSH) and Vitamin C.  Result: Administration of aqueous MC fruit extract significantly lowered the serum levels of TC and TG in group II as well as group IV rabbits. Administration of aqueous MC fruit extract significantly increased antioxidant capacity and decreased MDA and Atherogenic index of plasma (AIP) (AIP = log TG/HDL) in plasma. Conclusion: The results of the present study indicate that the potent therapeutic phytocomponents present in MC i.e. phytosterols, saponins, polyphenols, flavonoids and ascorbic acid, could be responsible for augmenting endogenous antioxidant system and decreasing lipid peroxidation in hypercholesteremic conditions.

Introduction

It is estimated that by 2020, coronary heart disease [CHD]   will be the largest cause of disability and death in India. Reddy et have  reported that prevalence  of  coronary  heart disease  in  adult  surveys  has  risen  four-fold  in  40  years  and  even  in  rural  areas  the prevalence  has  doubled  over  the  past  30  years (1).  Oxidative modification of low density lipoproteins (LDL) in the arterial wall by reactive oxygen species (ROS) plays a major role in   hypercholesterolaemia initiated atherosclerosis (2). Reduction in the endogenous antioxidant enzyme and  Increased lipid peroxidation due to  increased ROS generation have also  been implicated  in the pathogenesis of CHD with resultant vascular membrane damage (3). Pharmacological therapies to reduce lipid level , though effective, have limited patient compliance (4). Recent research indicates that foods rich in omega3 fatty acids, antioxidant vitamins and fibres may be beneficial for cardio-vascular health  and  thus the researchers have shifted their focus to   food products containing functional ingredients having antioxidant potential along with hypolipidemic activity (5).    

Momordica charantia (MC) is a member of cucurbitaceae family (also known as bitter gourd or karela), and is traditionally used as food in South Asia. The roots, leaves, seeds and fruits of this plant have been

used in traditional medicine for treating various diseases(6) . There are studies documenting  the hypoglycaemic (7), antipyretic, antibacterial(8), antihelminthic, antimalarial (9), antiulcerogenic (10) and immunomodulatory (11) properties of MC. The fruit is also rich in minerals, including potassium, calcium, magnesium, phosphorous and iron, and is a good source of dietary fibre (12).

 Shih et al demonstrated that bitter melon was effective in ameliorating the HF diet-induced hyperglycemia, hyperleptinemia, and decreased the levels of blood glycated hemoglobin (HbA1c) and free fatty acid (FFA) and concluded that bitter melon, is a food factor, but not a medicine, itself could influence dual PPAR alpha / PPAR gamma expression and the mediated gene expression, is effective in ameliorating insulin resistance and visceral obesity(13). Chan et al. have reported slower weight gain and reduced adiposity in rats fed on high-fat diet (HFD) supplemented with MC. They suggested that reduced adiposity was a consequence of increased lipid oxidation and mitochondrial uncoupling (14).  Since dyslipidemia along with lipid peroxidation is known to play a role in the development of atherosclerosis ,so the present study was planned  to evaluate the  effect of aqueous extract of MC on  atherogenic index, lipid peroxidation and antioxidant status  in diet-Induced hypercholesterolemia in rabbits.

Materials and Methods

Animals
Albino rabbits of either sex, weighing 1.5-2.5 kg, were used as subjects for this study. Animals were procured from the disease-free animal house of the CCS Haryana Agriculture University, Hisar, Haryana, India. They had free access to food and water and were maintained under 12:12 hour, light and dark cycles. The Institutional Animal Ethical Committee (IAEC) approved the experimental protocol and the animals were cared for as per the guidelines of CPCSEA, Department of Animal Welfare, Government of India.

Experimental Design

Rabbits were divided into four groups of six each, depending on the diet received.

Group I Control group).: The rabbits received standard chow diet throughout the experiment for 14 weeks.

Group II (MC group).: The rabbits received aqueous MC fruit extract (100 mg/kg, p.o.) daily throughout the experiment for 14 weeks .

Group III ( HFD group).: The rabbits received HFD[15] daily throughout the experiment for 14 weeks .

Group IV (HFD with MC group): The rabbits received aqueous MC fruit extract (100 mg/kg, p.o.) daily along with HFD for 14 weeks .

The composition of the two diets[15] was as follows:

Control diet: Wheat flour (22.5%), roasted Bengal gram powder (60%), skimmed milk powder (5%), casein (4%), refined oil (4%), salt mixture with starch (4%) and vitamins and choline mixture (0.5%).

HFD: Wheat flour (20.5%), roasted Bengal gram powder (52.6%), skimmed milk powder (5%), casein (4%), refined oil (4%), coconut oil (9%), salt mixture with starch (4%), vitamins and choline mixture (0.5%) and cholesterol (0.4%).

The aqueous extract from the powdered fruit of MC was prepared using the standard procedure. Oral dose of the extract was selected after a pilot study using three doses, i.e. 50, 75 and 100 mg/kg. All the drugs were administered orally (using an intragastric tube) in a single dose in the morning.

Sample collection

Blood samples were collected from the marginal vein of pinna of overnight fasted rabbits at the end of the experimental period. Lipid Profile, Malondialdehyde (MDA) and antioxidant parameters- GSH (Reduced glutathione) and Vitamin C were determined at the end of the study. The serum was separated immediately and assayed for the following parameters.

Total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C) and triglycerides (TGs) were estimated in the autoanalyser (KoneLab 30i, Trivitron) by enzymatic methods using kits supplied by Randox (16).    Atherogenic index of plasma (AIP), a marker of plasma atherogenicity on the basis of plasma lipids, was determined in all groups using the AIP=Log (TG/HDL) formula (17).

 Malondialdehyde (MDA): The lipid peroxidation products reacted with thiobarbituric acid (TBA) to give a red chromogen, which was measured at 535nm, spectrophotometrically (18).

Reduced Glutathione (GSH): Deproteinised serum was precipitated with metaphosphoric acid and was made to react with 5, 5’dithiobis-2-nitrobenzoic acid (DTNB) to produce a yellow chromogen, and absorbance was measured at 420nm against blank (19).

 Vitamin C: Ascorbic acid in the presence of Cu2+ was oxidized to dihydroascorbic acid which reacted with 2,4 dinitrophenylhydrazine (DNPH) to form a red bishydrazone with a maximum absorbance at 520nm, and thiourea was added to prevent oxidation of DNPH by any interfering substance (20).

Statistical analysis

The results were expressed as mean ± SEM of six rabbits in each group. The data were analysed statistically using the SPSS software version 14.0 in each group by applying Student’s (unpaired) ‘t’-test and p value < 0>

GroupLog (TG/HDL)

MDA

(nmol/ml)

GSH U mol/ml

Vit C

 mg/dl

Group I (control)0.3903.20 ± 0.750.60 ± 0.821.021 ± 0.50
Group II (MC)0.3222.40 ± 0.720.88 ± 0.0601.980 ± 0.46
Group III (HFD)0.6626.50 ± 0.780.391 ± 0.150.72 ± 0.42
Group IV (HFD +MC)0.378#4.32 ± 0.70#0.491 ± 0.28#0.86 ± 0.48#

* :- p

 # :- p< 0>

 # :- p< 0>

Table 1: Effect of aqueous Momordica charantia extract (100 mg/ kg, p.o.) on AIP,  MDA and antioxidant parameters in rabbits. Data are given as mean ± SEM (n=6 in each group).

Results

Administration of dietary cholesterol in group III animals significantly increased (p is less than 0.05) triglycerides ,cholesterol and lipid peroxidation (LPO) products as compared to control animals (group I) (Table 3). However, treatment with Momordica charantia (group IV) ameliorated dietary cholesterol-induced increase in MDA and atherogenic index . Hyperlipidemic oxidative stress led to depletion of endogenous antioxidant system (GSH, Vit C ) in group III animals as compared to control group animals. Supplementation of Momordica charantia (100mg/kg) in HFD diet reversed the adverse effect of high dietary cholesterol by normalizing these enzymic antioxidant indices.

Discussion

The atherogenic index of plasma (AIP), is the logarithm of molar ratio of triglyceridemia to high-density lipoprotein cholesterol (Log10TG/HDLcholesterol), is said to reflect the true relationship between protective and atherogenic lipoprotein and is thus considered as a reliable predictor of coronary heart disease (21) . Lowering of AIP as observed by Momordica charantia supplementation in group IV rabbits could be achieved only by lowering of plasma concentrations of atherogenic lipoproteins, particularly non-esterified plasma lipids such as triglycerides and total cholesterol; with corresponding elevation of plasma concentration of HDL-C as observed in the study. Chen and Li (22) have reported lower visceral fat and hepatic triglyceride content in the bitter melon fed rats and attributed it to enhanced sympathetic activity and lipolysis. A comprehensive array of antioxidant defence exists in mammalian cells comprising of both enzymatic and non-enzymatic molecules, which effectively neutralize reactive oxygen species (ROS) . Glutathione (GSH), a cysteine-containing tripeptide, is the most abundant non-protein thiol in mammalian cells and acts as primary line of defence to cope with deleterious effects of ROS ( 23).Decreased levels of glutathione in hypercholesterolemic animals (group II) indicates increased susceptibility to oxidative stress. Ascorbic acid (or vitamin C) is considered an important plasma antioxidant because of its fast reaction with many ROS and the poor reactivity of the resultant semidehydroascorbate radical (24). Diets rich in fruits and vegetables, and hence high in vitamin C, have been found to be associated with lower risk of cardiovascular diseases (25).

Superoxide anion, hydrogen peroxides and lipid hydroperoxides are produced in vivo in metabolic oxidation and trigger the function of membrane proteins , genetic material and lipids modifying their structure that may be exhibited in various forms of diseases including coronary artery disease(26). Hypercholesterolemia and lipid peroxidation are believed to be critically involved in development of Atherosclerosis (27). In our study a significant (p<0>

References

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