Evaluation of Antidiabetic, Phytochemical and Acute Toxicity of the Methanol Seed Extract of Senna occidentalis Linn

doi.org/10.26538/tjnpr/v5i6.20

Authors

  • Fave Y. Tata Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Maiduguri, Maiduguri, Nigeria
  • Fatima M. Danlamido Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Maiduguri, Maiduguri, Nigeria
  • Hafsat A. Sa’ab Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Maiduguri, Maiduguri, Nigeria
  • Musa A. Audu Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Maiduguri, Maiduguri, Nigeria
  • Abdulqadir B. Bababe Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Maiduguri, Maiduguri, Nigeria

Keywords:

Alloxan monohydrate, Acute toxicity, Diabetes, Methanol, Senna occidentalis

Abstract

Diabetes mellitus is one of the major chronic medical conditions. Many medicinal plants have demonstrated antidiabetic effect. The study evaluated the phytochemical constituents, acute toxicity and antidiabetic activity of the methanol seed extract of Senna occidentalis. Six groups of Wistar rats were used for the antidiabetic study. Group 1 was used as normal control while groups 2 and 3 were used for metformin and insulin as standard controls respectively. Groups 4, 5 and 6 were administered 200, 400 and 800 mg/kg of the methanol seed extract of S. occidentalis respectively through oral intubation. The study revealed the presence of carbohydrates, cardenolites, anthraquinones, flavonoids, tannins and triterpenoids. Alkaloids and saponins were not detected. The acute toxicity was greater than 4000 mg/kg body weight with no death during the 10 days observation after oral administration of the extract. The plant extract showed mild hypoglycaemic activity at the dose of 800 mg/kg at 12 hours by 3% and by 21% at 24 hours, slight decrease in blood glucose level was observed at 400 mg/kg by 2% and by 5% at 6 and 24 hours respectively. However, the extract showed no activity at 200 mg/kg throughout the study. The positive control (insulin) reduced the blood glucose level significantly by 65%, 57% and 36% at 3, 6 and 12 hours respectively but hypoglycaemic effect demonstrated by metformin throughout the study. The methanol seed extract of S. occidentalis showed mild hypoglycaemic activity. The extract contains phytochemical constituents that might be responsible for its antidiabetic activity. 

References

Chikezie PC, Ojiako OA, Nwufo KC. Overview of AntiDiabetic Medicinal Plants: The Nigerian Research Experience. J Diabet Metab. 2015; 6 (6):546.

Leng Y, Zhou X, Xie Z, Hu Z, Gao H, Liu X, Xie H, Fu X,Xie C. Efficacy and safety of Chinese herbal medicine on blood glucose fluctuations in patients with type 2 diabetes mellitus: A protocol of systematic review and metaanalysis. Med. 2020; 99:34.

Nasution BR, Aththorick TA, Rahayu S. Medicinal plants used in the treatment of diabetes in Karo ethnic, North Sumatra, Indonesia. Earth Environ Sci. 2018; 130:012038.

Narhe S, Kshirsagar SS, Patil VS. Review on Medicinal Herbs Used for Diabetes. Int J Pharm Clin Res. 2018; 10(8):224-228.

Bako SP, Bakfur MJ, John I, Bala EI. Ethnomedicinal and phytochemical profile of some savanna plant species in Nigeria. Int J Bot. 2005; 1(2):147-150.

Hussain A, Bose S, Wang JH, Yadav MK, Mahajan GB, Kim H. Fermentation, A Feasible Strategy for Enhancing Bioactivity of Herbal Medicines. Food Res Int. 2016; 81:1-16.

Sicree R., Shaw J, Zimmet P. The Global Burden. Diabetes and Impaired Glucose Tolerance. Prevalence and Projections. In: Gan, D. ed. Diabetes Atlas, 3rd edn. Brussels: International Diabetes Federation. 2006. 16-103 p.

Piero MN. Hypoglycemic effects of some Kenyan plants traditionally used in management of diabetes mellitus in eastern province, MSc thesis, Kenyatta University. 2006.

Orasanu G and Plutzky J. The pathologic continuum of diabetic vascular disease. J Am Coll Cardiol. 2009; 53 (5):35-42.

International Diabetes Federation. Diabetes Atlas, 7th ed., International Diabetes Federation, Brussels. 2015.

World Health Organization. Prevalence of diabetes in some African countries. 2016.

Akinkugbe OO, Yakubu AM, Johnson TO, Mabadaje AFB, Kaine WN, Ikeme AA. Non communicable disease in Nigeria. Spectrum Books Limited, Ibadan: 1992. 42-47 p.

Shaw JE, Sicree RA, Zimmet PZ. Global estimates for the prevalence of diabetes for 2010 and 2030. Diabet Res Clin Prac. 2010; 87:4-14.

Ali N, Shah SWA, Khan, Rehman S, Imran M, Hussian I, Shehbaz N, Jamshed H, Khan S. Pharmacotherapy-Based Problems in the Management of Diabetes Mellitus. J Young Pharm. 2010; 2(3):311-314.

Calixto JB. Twenty-five years of research on medicinal plants in Latin America: a personal view. J Ethnopharmacol. 2005; 100(1-2):131-134.

PROTA. Plant Resources of Tropical Africa. PROTA4U [Internet]. [cited 2019 Oct 21]. Available from: https://www.prota4u.org/database/searchresults.asp

Tona L, Cimanga RK, Mesia K, Musuamba CT, De Bruyne T, Apers S. In vitro antiplasmodial activity of extracts and fractions from seven medicinal plants used in the Democratic Republic of Congo. J Ethnopharmacol. 2004; 93:27-32.

Onakpa, MM and Ajagbonna OP. Antidiabetic potentials of Cassia occidentalis leaf extract on alloxan-induced diabeticalbino mice. Int J PharmTech Res. 2012; 4(4):1766-1769.

Trease GE and Evans WC. A test book of pharmacognosy, (15th edition). Elsevier Company, Philadelphia, USA. 2002. 191-148p.

Sofowora EA. Medicinal and Traditional Meidicine in Africa, (3rd edition). Spectrum book Ltd Ibadan, Nigeria. 2008. 89-133 p.

OECD Guidelines for the testing of chemicals, Acute oral Toxicity-Up-and-Down-Procedure(UDP). 425, OECD. 2008.

Lenzen S. Alloxan and streptozotocin diabetes. Adv Res InstDiabet Anim. 2010; 6(4):113-122.

Kathirvel A and Sujatha V. Phytochemical studies of Cassia occidentalis Linn. Flowers and seeds in various solvent extracts. Int J Pharmacogn Phytochem Res. 2011; 3(4):95-101.

Usha K, Kasturi GM, Hemalata P. Hepatoprotective effect of Hogrophila spinosa and Cassia occidentalis on carbon tetrachloride induced liver damage in experimental rats. Indian J Clin Biochem. 2007; 22(2):132-135.

Garba R, Saidu AN, Adeyemi HRY, Muhammad HL. Effect of methanolic extract of Cassia occidentalis L. Root bark on body weight and selected biochemical parameters in alloxan-induced diabetic rats. Br J Pharmacol Toxicol. 2015; 6(2):39-49.

Yadav JP, Arya V, Yadav S, Panghal M, Kumar SD. S. occidentalis: A review on its ethnobotany, phytochemical and pharmacological process. Fitoter. 2009; 81:223-230.

Gupta A, Naraniwal M, Kothari V. Modern extraction methods for preparation of bioactive plant extracts. Int J Appl Nat Sci. 2012; 1(1):8-26.

Rahman AU and Zaman K. Medicinal plants with hypoglycaemic activity. J Ethnopharmacol. 1989; 26:1-55.

Mirtes GB, Silva T, Aragao PS, Lafayette SL. Acute and subacute toxicity of C. occidentalis L. stem and leaf in wistar rats. J Ethnopharmacol. 2011; 136 (2):241-346.

Saurabh A, Jogender S, Sumer S. Antidiabetic activities of Cassia occidentalis. Rec Res Sci Technol. 2013; 5(1):51-53.

Emmanuel S, Sheeba MR, Sreekanth MR. Antidiabetic activity of Cassia occidentalis Linn. in streptozotocininduced diabetic rats: A dose dependent study. Int J Pharm Biosci. 2010; 1(4):14-25.

Amuri B, Maseho M, Simbi L, Okusa P, Duez P, Byanga K. Hypoglycemic and Antihyperglycemic Activities of Nine Medicinal Herbs Used as Antidiabetic in the Region of Lubumbashi. Phytother Res. 31(7); 2017:1029-1033

Rios JL, Francini F, Schinella GR. Natural products for treatment of type 2 diabetes mellitus. Planta Med. 2015; 81:975-994.

Laxmi V, Anirudh K, Basant KP, Rajesh SP. Antidiabetic activity of Cassia occidentalis (Linn) in normal and alloxan-induced diabetic rats. Indian J Pharmacol. 2010; 42 (4): 221-228.

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Published

2021-06-01

How to Cite

Tata, F. Y., Danlamido, F. M., Sa’ab, H. A., Audu, M. A., & Bababe, A. B. (2021). Evaluation of Antidiabetic, Phytochemical and Acute Toxicity of the Methanol Seed Extract of Senna occidentalis Linn: doi.org/10.26538/tjnpr/v5i6.20. Tropical Journal of Natural Product Research (TJNPR), 5(6), 1101–1105. Retrieved from https://tjnpr.org/index.php/home/article/view/632