Phytochemical Screening, Invitro Antioxidant and In-vivo Antidiabetic Activity of Methanolic Extract of Leaves of Celastrus paniculatus

Main Article Content

Aeshwarya Joshi
Jyoti Menariya

Abstract

Celastrus paniculatus Willd, commonly known as Staff tree, is a plant species from the Celastraceae family. It contains various active constituents, including celapanigin, malkangunin, celapanin, and zeylasteral, which contribute to its medicinal properties. The objective of this study was to evaluate the qualitative and quantitative phytochemical analysis, in vitro antioxidant activities, and in vivo anti-diabetic potentials of the methanolic extract of C. paniculatus leaves using a streptozotocin-induced rat model. The in vitro antioxidant activity of the methanolic extract was assessed using DPPH and ABTS radical cation decolorization assay methods. Rats were induced with diabetes using streptozotocin and treated with glibenclamide as the standard medication. Body weight and blood sugar levels were measured throughout the study. Phytochemical analysis revealed the presence of alkaloids, glycosides, proteins and amino acids, flavonoids, tannins and phenolic compounds, saponins, triterpenoids, and steroids in the leaves. The total phenolic content of the methanolic extract was 32.33 mg/g, followed by flavonoids at 11.66 mg/g. Oral treatment with the methanolic extract of C. paniculatus at doses of 200 and 400 mg/kg significantly reduced blood glucose levels in diabetic rats compared to control rats (p < 0.001) and increased body weight. The chemical constituents of the plant extract may have potential in preventing diabetic complications and could serve as an alternative in the current range of antidiabetic drugs. Further research is recommended to validate the use of this plant as an antidiabetic agent

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How to Cite
Aeshwarya Joshi, & Jyoti Menariya. (2023). Phytochemical Screening, Invitro Antioxidant and In-vivo Antidiabetic Activity of Methanolic Extract of Leaves of Celastrus paniculatus. Journal of Advanced Zoology, 44(5), 1194–1202. https://doi.org/10.53555/jaz.v44i5.3561
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Articles
Author Biographies

Aeshwarya Joshi

Assistant Professor, Department of Pharmacy, Sangam University, Rajasthan, India

Jyoti Menariya

Associate Professor, Department of Pharmacy, Geetanjali University, Rajasthan, India

References

Shihabudeen MS, Priscilla HHD, Thirumurugan K, Antimicrobial activity and phytochemical analysis of selected Indian folk medicinal plants, International Journal of Pharma Sciences and Research, 1, 2010, 430-434.

Cook N. Flavonoids--Chemistry, metabolism, cardioprotective effects, and dietary sources. J Nutr Biochem. 1996; 7(2):66–76.

Kumpulainen JT, Salonen JT. Natural Antioxidants and Anticarcinogens in Nutrition, Health and Disease 1999.

Tanaka T, Kusano R, Kouno I. Synthesis and antioxidant activity of novel amphipathic derivatives of tea polyphenol. Bioorg Med Chem Lett 1998; 8(14):1801–6.

Young IS. Antioxidants in health and disease. J Clin Pathol 2001; 54(3):176–86.

Halliwell B. Free radicals, antioxidants, and human disease: curiosity, cause, or consequence? Lancet 1994; 344(8924):721–4.

Halliwell B. Biochemistry of oxidative stress: Figure 1. Biochem Soc Trans 2007; 35(5):1147–50.

Singh M and Naithani M. Phytochemical estimation and antioxidant activity of seed extract of millets traditionally consumed by common people of Uttrakhand, India. Int.J .Biol .Pharm .Allied Sci... 2014; 3(10): 2389-400.

Litescu SC, Sandra AV Eremia, SAV, Diaconu M, Tache A and RaduG.L. Biosensors Applications on Assessment of Reactive Oxygen Species and Antioxidants. In: Vernon Somerset, editor. Environmental Biosensors.In tech open 2011,p 95-114

Ramadan-Hassanien MF. Total antioxidant potential of juices, beverages and hot drinks consumed in Egypt screened by DPPH in vitro assay. Grasas y Aceites 2008; 59(3):254–9.

Suhaj M. Spice antioxidants isolation and their antiradical activity: a review. J Food Compos Anal. 2006; 19(6–7):531–7.

Eseyin O, Ebong P, Eyong E, Awofisayo O, Agboke A. Effect of Telfairia occidentalis on oral glucose tolerance in rats. Afr J Pharm Pharmacol 2010; 4: 368-372.

Patel DK, Prasad SK, Kumar R, Hemalatha S. An overview on antidiabetic medicinal plants having insulin mimetic property. Asian Pac J Trop Biomed 2012; 2: 320-330.

Rajan M, Kumar VK, Kumar PS, Swathi KR, Haritha S. Antidiabetic, antihyperlipidaemic and hepatoprotective activity of methanolic extract of Ruellia tuberose Linn. leaves in normal and alloxan induced diabetes. J Chem Pharm Res 2012; 4: 2860-2868.

Rajasekar V, Kirbanandan S, Lakshmi BS. Assessment of antidiabetic activity of Syzygium jambolanum using in vitro model. Am J Infect Dis 2010; 5: 99-105.

Malviya N, Jain S, Malviya S. Antidiabetic potential of medicinal plants. Acta Pol Pharm 2010; 67: 113-118.

Dangi KS, Mishra SN. Antihyperglycemic, antioxidant and hypolipidemic effect of Capparis aphylla stem extracts in streptozotocin induced diabetic rats. Biol Med 2010; 2: 35-44.

Yalniz M, Pour P M (2006) Toxicology of the endocrine pancreas. Taylor and Francis group, Boca Raton, Florida, USA, 542-545.

Ghasemi A, Khalifi S, Jedi S (2014) Streptozotocin-nicotinamide-induced rat model of type 2 diabetes (review). Acta Physiol Hung 101: 408-420.

Nayak Y, Hillemane V, Daroji VK, Jayashree BS, Unnikrishnan MK (2014) Antidiabetic activity of benzopyrone analogues in nicotinamide-streptozotocin induced type 2 diabetes in rats. The Scientific World Journal.

Eleazu CO, Eleazu KC, Chukwuma S, Essien UN (2013) Review of the mechanism of cell death resulting from streptozotocin challenge in experimental animals, its practical use and potential risk to humans. J Diabetes Metab Disord 12: 60.

Sharada M, Ahuja A, Kaul MK (2003) Regeneration of plantlets via callus cultures in Celastrus paniculatus Willd-A rare endangered medicinal plant. J Plant Bio Chem Biotech 12(1):65–69.

Khanna C (2007) Conservation of some useful medicinal plants of Haridwar district in Uttaranchal state. Medicinal Plants: Conservation and Cultivation, Uttaranchal, pp 147–166

Mude N, Ingle A, Gade A, Rai M (2009) Synthesis of silver nanoparticles using callus extract of Carica papaya—a first report. J Plant Biochem Bio Tech 18(1):83–86.

Jain DK, Gupta S, Jain R, Jain N. Anti-inflammatory Activity of 80% Ethanolic Extract of Acorus calamus Linn. Leaves in Albino Rats. Research J. Pharm. and Tech 2010; 3 (3): 882-884.

Dutta R, Sharma MK, Khan A, Jha M. Phytochemical and in vitro antioxidant assay of Fumaria officinalis leaf extract. Journal of Advanced Scientific Research. 2020 Aug 10; 11(03):176-82.

Gadekar S, Goyal S, Khan A, Jha M. Chemopreventive action of sphaeranthus indicus on dmba-induced skin papillomagenesis in mice. Journal of Advanced Scientific Research. 2020; 11(3):161-167.

Pradhan A, Jain P, Pal M, Chauhan M, Jain DK. Qualitative and quantitative determination of phytochemical contents of hydroalcoholic extract of salmalia malabarica. Pharmacologyonline 2019; 1:21-26.

Joshi S, Parkhe G, Aqueel N, Dixit N, Jain DK. Estimation of total phenolic, total flavonoids and total protein content of hydroalcoholic extract of Anacyclus pyrethrum. Pharmacologyonline 2019; 1:27-33.

Gulçin I, Elias R, Gepdiremen A, Boyer L. Antioxidant activity of lignans from fringe tree (Chionanthus virginicus L.). Eur Food Res Technol 2006; 223: 759-767.

Zheleva-Dimitrova D, Nedialkov P, Kitanov G. Radical scavenging and antioxidant activities of methanolic extracts from Hypericum species growing in Bulgaria. Pharmacogn Mag. 2010 Apr;6(22):74–8.

Etuk EU. Animals models for studying diabetes mellitus. Agric Biol JN Am. 2010;1(2):130–4.

Kumar S, Kumar V, Prakash OM. Antidiabetic and hypolipidemic activities of Kigelia pinnata flowers extract in streptozotocin induced diabetic rats. Asian Pac J Trop Biomed. 2012;2(7):543–6.

Jag Mohan. Organic spectroscopy principles and applications, Narosa publishing House, Daryagani, Delhi, 2005, 2Edn.

Halliwell B, Gutteridge JM, Aruoma OI. The deoxyribose method: a simple "test-tube" assay for determination of rate constants for reactions of hydroxyl radicals, Anal Bio chem. 1987; 165:215-9.

Szkudelski T. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiol Res 2001; 50:536‑46.

Cheng D, Liang B, Li Y. Antihyperglycemic effect of Ginkgo biloba extract in streptozotocin‑induced diabetes in rats. Biomed Res Int 2013; 2013:162724.

Wilcox G. Insulin and Insulin Resistance. Clin Biochem Rev 2005; 26:19‑39.