Hypolipidemic activity of Hiptage benghlensis leaf extracts on high fat diet induced hyperlipidaemic rats

Authors

  • Pradeep Kumar Samal Department of Pharmacy, Guru Ghasidas Vishwavidyalaya (A Central University), Bilaspur-495009, Chhattisgarh, India
  • Kedar Prasad Meena Department of Pharmacy, Guru Ghasidas Vishwavidyalaya (A Central University), Bilaspur-495009, Chhattisgarh, India
  • Jaya Shree Department of Pharmacology, Shir Shankaracharya College of Pharmaceutical Sciences, Shri Shankaracharya Professional University, Bhilai-490020, Chhattisgarh, India
  • Rajesh Choudhary Department of Pharmacology, Shir Shankaracharya College of Pharmaceutical Sciences, Shri Shankaracharya Professional University, Bhilai-490020, Chhattisgarh, India

Abstract

The present study was designed to evaluate the hypolipidemic effects of aqueous extract (HBAE) and ethanolic extract (HBEE) of leaves of Hiptage benghalensis by using high-fat-diet induced hyperlipidemic animal model. Albino male Wistar rats (120-150 g) were split into various groups, each of which had six individuals. Normal rats (group I) were received 0.3% Carboxy methyl cellulose (CMC) with standard laboratory diet, while hyperlipidemic rats (group II, III, IV, V, VI and VII) were fed high fat diet for induction of hyperlipidemia. Hyperlipidaemic control group (group II) received 0.3% CMC (10 ml/kg/day), standard group (group III) received gemfibrozil (50 mg/kg/day, p.o.), HBAE groups (group IV and V) received aqueous extract of Hiptage benghalensis (100 and 200 mg/kg/day, p.o.), and HBEE groups (group VI and VII) received ethanolic extract of Hiptage benghalensis (100 and 200 mg/kg/day, p.o.), concurrent with high fat diet for consecutive four weeks. The HBAE and HBEE treatments led to significant (P < 0.05) reduction in serum lipids (TC, TG, LDL and VLDL) and elevation in cardio protective HDL, when compared to hyperlipidaemic rats (group II). Phytochemical screening revealed the presence of phytoconstituents such as alkaloids, flavonoids, saponins, tannins, phenolic compounds and steroids, which may be attributed to observed hypolipidemic effects. The findings of the present study concluded that HBEE (200 mg/kg, p.o.) had potent hypolipidemic effects.

Keywords:

Hiptage benghalensis; Hyperlipidemia; High fat diets; Cholesterol, Triglycerides

DOI

https://doi.org/10.25004/IJPSDR.2023.150316

References

Nelson RH. Hyperlipidemia as a risk factor for cardiovascular disease. Primary care. 2013;40:195-211. doi: 10.1016/j.pop.2012.11.003.

Pirillo A, Casula M, Olmastroni E, Norata GD, Catapano AL. Global epidemiology of dyslipidaemias. Nature reviews Cardiology. 2021;18:689-700. doi: 10.1038/s41569-021-00541-4.

Ward NC, Watts GF, Eckel RH. Statin Toxicity. Circulation Research. 2019;124:328-50. doi.org/10.1161/CIRCRESAHA.118.312782.

Zhang X, Wu C, Wu H, Sheng L, Su Y, Zhang X, Luan H, Sun G, Sun X, Tian Y, et al. Anti-hyperlipidemic effects and potential mechanisms of action of the caffeoylquinic acid-rich Pandanus tectorius fruit extract in hamsters fed a high fat-diet. PloS one. 2013;8:e61922. doi: 10.1371/journal.pone.0061922.

Alsheikh-Ali AA, Kuvin JT, Karas RH. Risk of adverse events with fibrates. The American journal of cardiology. 2004;94:935-8. doi:10.1016/j.amjcard.2004.06.033.

Babu Rao B, Narsimha Reddy Y. Evaluation of AntiCancer Activity of Methanolic Extract of Hiptage benghalensis (L.) Kurz on Cancer Cell Lines. Pharmacogn Res. 2018;10.DOI:10.4103/pr.pr_102_17

Maheshwari P, Baburao B, Reddy ARN. Hepatoprotective activity of methanolic extract of Hiptage bengalensis leaves against CCl4-induced hepatotoxicity in rats. Toxicol Mech Methods. 2012;22:483-87.doi: 10.3109/15376516.2012.674068

Chenthurpandy P, Kalidass C, Mohan VJPJ. Pharmacognostical Investigation of Hiptage benghalensis (L.) Kurz. (Malpighiaceae). Pharmacognosy Journal. 2009;1:103-05.

Murugan M MVR. Evaluation of phytochemical analysis and antibacterial activity of Bauhinia purpurea L. and Hiptage benghalensis L. Kurz. Journal of Applied Pharmaceutical Science. 2011;1:157-60.

Koshy AS, Anila L, Vijayalakshmi NR. Flavonoids from Garcinia cambogia lower lipid levels in hypercholesterolemic rats. Food Chemistry. 2001;72:289-94.DOI:10.1016/S0308-8146(00)00225-9.

Chen J, Li X. Hypolipidemic effect of flavonoids from mulberry leaves in triton WR-1339 induced hyperlipidemic mice. Asia Pacific journal of clinical nutrition. 2007;16 Suppl 1:290-4.DOI:10.6133/APJCN.2007.16.S1.55

Althwab SA, Alamro SA, Al Abdulmonem W, Allemailem KS, Alarifi SA, Hamad EM. Fermented camel milk enriched with plant sterols improves lipid profile and atherogenic index in rats fed high -fat and -cholesterol diets. Heliyon. 2022;8:e10871.

Handa SS, Khanuja SPS, Longo G, Rakesh BP. Extraction Technology for Medicinal and Aromatic Plants. Trieste: International Centre for Science and High Technology; 2008.

Iqbal E, Salim KA, Lim LBL. Phytochemical screening, total phenolics and antioxidant activities of bark and leaf extracts of Goniothalamus velutinus (Airy Shaw) from Brunei Darussalam. J King Saud Univ Sci. 2015;27:224-32.doi.org/10.1016/j.jksus.2015.02.003

Allain CC, Poon LS, Chan CS, Richmond W, Fu PC. Enzymatic determination of total serum cholesterol. Clinical chemistry. 1974;20:470-5.DOI:10.1093/CLINCHEM/20.4.470.

McGowan MW, Artiss JD, Strandbergh DR, Zak B. A peroxidasecoupled method for the colorimetric determination of serum triglycerides. Clinical chemistry. 1983;29:538-42. DOI:10.1093/CLINCHEM/29.3.538

Assmann G. [Current diagnosis of hyperlipidemias]. Der Internist. 1979;20:559-64.

Barham D, Trinder P. An improved colour reagent for the determination of blood glucose by the oxidase system. The Analyst. 1972;97:142-5. doi: 10.1039/an9729700142.

Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical chemistry. 1972;18:499-502.doi :org/10.1093/clinchem/18.6.499

Rolls BJ, Morris EL, Roe LS. Portion size of food affects energy intake in normal-weight and overweight men and women. The American journal of clinical nutrition. 2002;76:1207-13. doi: 10.1093/ajcn/76.6.1207.

Devlin MJ, Yanovski SZ, Wilson GT. Obesity: what mental health professionals need to know. The American journal of psychiatry. 2000;157:854-66.doi: 10.1176/appi.ajp.157.6.854.

Jeannie C, Genesio MK, Laura AC, John LV. Animal Models of Diet-induced Hypercholesterolemia. In: Sekar Ashok K, editor. Hypercholesterolemia. Rijeka: IntechOpen; 2015. p. Ch. 1. DOI:10.5772/59610

Pellizzon M. Diet-Induced Atherosclerosis/Hypercholesterolemia in Rodent Models. Research Diets, Inc. 2009.

Cao L, Liu X, Cao H, Lv Q, Tong N. Modified high-sucrose diet-induced abdominally obese and normal-weight rats developed high plasma free fatty acid and insulin resistance. Oxidative medicine and cellular longevity. 2012;2012:374346.doi: 10.1155/2012/374346

Santuré M, Pitre M, Marette A, Deshaies Y, Lemieux C, Larivière R, Nadeau A, Bachelard H. Induction of insulin resistance by highsucrose feeding does not raise mean arterial blood pressure but impairs haemodynamic responses to insulin in rats. British journal of pharmacology. 2002;137:185-96.doi: 10.1038/sj.bjp.0704864

Hariri N, Thibault L. High-fat diet-induced obesity in animal models. Nutrition research reviews. 2010;23:270-99.doi: 10.1017/S0954422410000168.

NCEPE. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection. Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation. 2002;106:3143-421.

Bainton D, Miller NE, Bolton CH, Yarnell JW, Sweetnam PM, Baker IA, Lewis B, Elwood PC. Plasma triglyceride and high density lipoprotein cholesterol as predictors of ischaemic heart disease in British men. The Caerphilly and Speedwell Collaborative Heart Disease Studies. British heart journal. 1992;68:60-6. doi: 10.1136/hrt.68.7.60.

Zhang AH, Gao S, Fan JL, Huang W, Zhao TQ, Liu G. Increased plasma HDL cholesterol levels and biliary cholesterol excretion in hamster by LCAT overexpression. FEBS letters. 2004;570:25-9.doi: 10.1016/j.febslet.2004.06.017.

Devi R, Sharma DK. Hypolipidemic effect of different extracts of Clerodendron colebrookianum Walp in normal and high-fat diet fed rats. J Ethnopharmacol. 2004;90:63-68.doi: 10.1016/j.jep.2003.09.022.

Rousset X, Vaisman B, Amar M, Sethi AA, Remaley AT. Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease. Current opinion in endocrinology, diabetes, and obesity. 2009;16:163-71.doi: 10.1097/med.0b013e328329233b.

Harchaoui KE, Visser ME, Kastelein JJ, Stroes ES, Dallinga-Thie GM. Triglycerides and cardiovascular risk. Current cardiology reviews. 2009;5:216-22.doi: 10.2174/157340309788970315

Kunutsor SK, Zaccardi F, Karppi J, Kurl S, Laukkanen JA. Is High Serum LDL/HDL Cholesterol Ratio an Emerging Risk Factor for Sudden Cardiac Death? Findings from the KIHD Study. Journal of atherosclerosis and thrombosis. 2017;24:600-08.

Castelli WP, Garrison RJ, Wilson PW, Abbott RD, Kalousdian S, Kannel WB. Incidence of coronary heart disease and lipoprotein cholesterol levels. The Framingham Study. Jama. 1986;256:2835-8. doi: 10.5551/jat.37184

Vijaya C, Ramanathan M, Suresh B. Lipid lowering activity of ethanolic extract of leaves of Aegle marmelos (Linn.) in hyperlipidaemic models of Wistar albino rats. Indian journal of experimental biology. 2009;47:182-5.

Weggemans RM, Trautwein EA. Relation between soy-associated isoflavones and LDL and HDL cholesterol concentrations in humans: a meta-analysis. European journal of clinical nutrition. 2003;57:940-6.doi: 10.1038/sj.ejcn.1601628.

Moreno-Fernández S, Garcés-Rimón M, Vera G, Astier J, Landrier JF, Miguel M. High Fat/High Glucose Diet Induces Metabolic Syndrome in an Experimental Rat Model. Nutrients. 2018;10.doi: 10.3390/nu10101502.

Shi Y, Guo R, Wang X, Yuan D, Zhang S, Wang J, Yan X, Wang C. The regulation of alfalfa saponin extract on key genes involved in hepatic cholesterol metabolism in hyperlipidemic rats. PloS one. 2014;9:e88282.doi: 10.1371/journal.pone.0088282

Jesch ED, Carr TP. Food Ingredients That Inhibit Cholesterol Absorption. Preventive nutrition and food science. 2017;22:67-80. doi: 10.3746/pnf.2017.22.2.67

Yin P, Zhao S, Chen S, Liu J, Shi L, Wang X, Liu Y, Ma C. Hypoglycemic and hypolipidemic effects of polyphenols from burs of Castanea mollissima Blume. Molecules (Basel, Switzerland). 2011;16:9764-74. doi: 10.3390/molecules16119764

Kaamanen M, Adlercreutz H, Jauhiainen M, Tik kanen MJ. Accumulation of genistein and lipophilic genistein derivatives in lipoproteins during incubation with human plasma in vitro. Biochimica et biophysica acta. 2003;1631:147-52.

Khare CP. Indian Medicinal Plants: An Illustrated Dictionary. New York: Springer; 2007.

Lees AM, Mok HY, Lees RS, McCluskey MA, Grundy SM. Plant sterols as cholesterol-lowering agents: clinical trials in patients with hypercholesterolemia and studies of sterol balance. Atherosclerosis. 1977;28:325-38. doi: 10.1016/s1388-1981(02)00363-3.

Mattson FH, Grundy SM, Crouse JR. Optimizing the effect of plant sterols on cholesterol absorption in man. The American journal of clinical nutrition. 1982;35:697-700. doi: 10.1093/ajcn/35.4.697.

Published

30-05-2023
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“Hypolipidemic Activity of Hiptage Benghlensis Leaf Extracts on High Fat Diet Induced Hyperlipidaemic Rats”. International Journal of Pharmaceutical Sciences and Drug Research, vol. 15, no. 3, May 2023, pp. 350-5, https://doi.org/10.25004/IJPSDR.2023.150316.

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Research Article

How to Cite

“Hypolipidemic Activity of Hiptage Benghlensis Leaf Extracts on High Fat Diet Induced Hyperlipidaemic Rats”. International Journal of Pharmaceutical Sciences and Drug Research, vol. 15, no. 3, May 2023, pp. 350-5, https://doi.org/10.25004/IJPSDR.2023.150316.