Hypoglycaemic, Hypolipidaemic and Antioxidant Properties of Celastrus paniculatus Seed Extract in STZ-induced Diabetic Rats

Md Fahim Ahmad, Md Ali Haidar, Nida Naseem, Haseeb Ahsan, Waseem Ahmad Siddiqui

Abstract


Background: Celastrus paniculatus is a herb used in the Ayurvedic system of medicine that has been reported to show multiple pharmacological properties. In this study, we explored the antioxidative, hypolipidaemic and hypoglycaemic potential of C. paniculatus methanolic seed extract (CPMSE) in high-fat diet (HFD)/streptozotocin (STZ)-induced type 2 diabetes mellitus (T2DM) rats.

Materials and methods: Seeds of C. paniculatus were extracted in methanol using Soxhlet extraction method. A total of 36 rats were induced with STZ and HFD and treated with glibenclamide or various concentrations of CPMSE. Upon treatment, blood samples were collected and kidney and liver samples were homogenised. Serum biochemical estimation was performed using several diagnostic kits. Protein was estimated by bicinchoninic acid (BCA) method. Oxidative stress was assessed by measuring malondialdehyde level and superoxide dismutase (SOD), catalase (CAT) and glutathione-S-transferase (GST) activity.

Results: CPMSE caused improvements in glucose homeostasis, lipid profile, liver function and oxidative stress parameters in a dose-dependent manner. CPMSE significantly decreased the levels of fasting blood glucose and glycated haemoglobin as well as increased insulin level and total protein content. There was an increase in total cholesterol (TC), low density lipoprotein-cholesterol (LDL-C), triglycerides (TG) levels and reduction in high density lipoprotein-cholesterol (HDL-C) level. There was a decrease in serum levels of serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate transaminase (SGOT) and alkaline phosphatase (ALP). CPMSE decreased LPO and increased CAT, SOD and GST activity.

Conclusion: CPMSE has hypoglycaemic, hypolipidaemic and antioxidant properties by reducing the oxidative stress.

Keywords: diabetes mellitus, Celastrus paniculatus, antioxidant, phytochemicals, phytonutrients, streptozotocin, high-fat diet


Full Text:

PDF

References


Olokoba AB, Obateru OA, Olokoba LB. Type 2 diabetes mellitus: A review of current trends. Oman Med J. 2012; 27(4): 269-73, CrossRef.

Goyal R, Jialal I. Diabetes Mellitus Type 2. Treasure Island: StatPearls; 2022, article.

Khan MAB, Hashim MJ, King JK, Govender RD, Mustafa H, Al Kaabi J. Epidemiology of type 2 diabetes - Global burden of disease and forecasted trends. J Epidemiol Glob Health. 2020; 10(1): 107-11, CrossRef.

Kartika R, Wibowo H. Impaired function of regulatory T cells in type 2 diabetes mellitus. Mol Cell Biomed Sci. 2020; 4(1): 1-9, CrossRef.

Zimmet PZ. Diabetes and its drivers: The largest epidemic in human history? Clin Diabetes Endocrinol. 2017; 3: 1, CrossRef.

Riaz M, Zia-Ul-Haq M, Saad B. Anthocyanins and Human Health: Biomolecular and Therapeutic Aspects. Cham: Springer; 2016, article.

Defronzo RA. From the triumvirate to the ominous octet: A new paradigm for the treatment of type 2 diabetes mellitus. Diabetes. 2009; 58(4): 773-95, CrossRef.

Galtier F. Definition, epidemiology, risk factors. Diabetes Metab. 2010; 36(6 Pt 2): 628-51, CrossRef.

Salim B. Diabetes mellitus and its treatment. Int J Diabetes Metab. 2005; 13: 111-34, CrossRef.

Adewole SO, Caxton-Martins EA, Ojewole JA. Protective effect of quercetin on the morphology of pancreatic β-cells of streptozotocin-treated diabetic rats. Afr J Trad Complement Alt Med. 2006; 4(1): 64-74, CrossRef.

Parimelazhagan T. Medicinal Plants: Promising Future for Health and New Drugs. Boca Raton: CRC Press; 2018, article.

Mukherjee PK, Maiti K, Mukherjee K, Houghton PJ. Leads from Indian medicinal plants with hypoglycemic potentials. J Ethnopharmacol. 2006; 106(1): 1-28, CrossRef.

Arora N, Rai SP. Celastrus paniculatus, an endangered Indian medicinal plant with miraculous cognitive and other therapeutic properties: An overview. Int J Pharm Bio Sci. 2012; 3(3): 290-303, article.

Aleem M. Phytochemistry and pharmacology of Celastrus paniculatus Wild.: A nootropic drug. J Complement Integr Med. 2021; ahead of print, CrossRef.

Harish BG, Krishna V, Santosh Kumar HS, Khadeer Ahamed BM, Sharath R, Kumara Swamy HM. Wound healing activity and docking of glycogen-synthase-kinase-3-beta-protein with isolated triterpenoid lupeol in rats. Phytomedicine. 2008; 15(9): 763-7, CrossRef.

Shen Y, Chen BL, Zhang QX, Zheng YZ, Fu Q. Traditional uses, secondary metabolites, and pharmacology of Celastrus species - A review. J Ethnopharmacol. 2019; 241: 111934, CrossRef.

Rafieian-Kopaei M, Setorki M, Doudi M, Baradaran A, Nasri H. Atherosclerosis: Process, indicators, risk factors and new hopes. Int J Prev Med. 2014; 5(8): 927-46, article.

Barham D, Trinder P. An improved colour reagent for the determination of blood glucose by the oxidase system. Analyst. 1972; 97(151): 142-5, CrossRef.

Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974; 47(3): 469-74, CrossRef.

Claiborne A. Catalase activity. In: Greenwald RA, editor. CRC Handbook of Methods for Oxygen Radical Research. Boca Raton: CRC Press; 1985, article.

Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases: The first enzymatic step in mercapturic acid formation. J Biol Chem. 1974; 249(22): 7130-39, article.

Ramaiah CV, Kumar GS, Rajendra W. Traditional, ethnomedical, and pharmacological uses of Celastrus paniculatus: Review. Asian J Pharmaceut. 2019; 12(4): S1119-S26, article.

Oh PS, Lee SJ, Lim KT. Hypolipidemic and antioxidative effects of the plant glycoprotein (36 kDa) from Rhus verniciflua stokes fruit in Triton WR-1339-induced hyperlipidemic mice. Biosci Biotechnol Biochem. 2006; 70(2): 447-56, CrossRef.

Patil RH, Prakash K, Maheshwari VL. Hypolipidemic effect of Celastrus paniculatus in experimentally induced hypercholesterolemic Wistar rats. Indian J Clin Biochem. 2010; 25(4): 405-10, CrossRef.

Upadhyay RK. Emerging risk biomarkers in cardiovascular diseases and disorders. J Lipids. 2015; 2015: 971453, CrossRef.

Abiola TS, David OO, Olatunde FE. Effect of tannin-rich extract of Chasmanthera dependens on piroxicam-induced liver damage in male Wistar rats. Mol Cell Biomed Sci. 2021; 5(1): 27-36, CrossRef.

Taghavi F, Moosavi-Movahedi AA. Free radicals, diabetes, and its complexities. In: Ozturk MA, Hakeem KR, editors. Plant and Human Health, Vol 2. Cham: Springer; 2019. p. 1-41, article.

Rösen P, Nawroth PP, King G, Möller W, Tritschler HJ, Packer L. The role of oxidative stress in the onset and progression of diabetes and its complications: A summary of a Congress Series sponsored by UNESCO-MCBN, the American Diabetes Association and the German Diabetes Society. Diabetes Metab Res Rev. 2001; 17(3): 189-212, CrossRef.

Helou C, Marier D, Jacolot P, Abdennebi-Najar L, Niquet-Léridon C, Tessier FJ, et al. Microorganisms and Maillard reaction products: A review of the literature and recent findings. Amino Acids. 2014; 46(2): 267-77, CrossRef.

Negre-Salvayre A, Salvayre R, Augé N, Pamplona R, Portero-Otín M. Hyperglycemia and glycation in diabetic complications. Antioxid Redox Signal. 2009; 11(12): 3071-109, CrossRef.

Ayala A, Muñoz MF, Argüelles S. Lipid peroxidation: Production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev. 2014; 2014: 360438, CrossRef.

Jusup I, Batubara L, Ngestiningsih D, Fulyani F, Paveta DA, Bancin PTLA. Association between malondialdehyde, GSH/GSSG ratio and bone mineral density in postmenopausal women. Mol Cell Biomed Sci. 2021; 5(1): 13-7, CrossRef.

Tiwari M, Kakkar P. Plant derived antioxidants - Geraniol and camphene protect rat alveolar macrophages against t-BHP induced oxidative stress. Toxicol In Vitro. 2009; 23(2): 295-301, CrossRef.

Kandikattu HK, Venuprasad MP, Pal A, Khanum F. Phytochemical analysis and exercise enhancing effects of hydroalcoholic extract of Celastrus paniculatus Willd. Ind Crops Prod. 2014; 55: 217-24, CrossRef.

Kurutas EB. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: Current state. Nutr J. 2016; 15(1): 71, CrossRef.




DOI: https://doi.org/10.21705/mcbs.v7i1.282

Copyright (c) 2023 Cell and BioPharmaceutical Institute

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Indexed by:

               

                      


Cell and BioPharmaceutical Institute