Evaluation of Antidiabetic Activity of Corchorus trilocularis Linn Plant Extract
Pharmaceutical Science-Pharmacology
DOI:
https://doi.org/10.22376/ijpbs/lpr.2022.12.5.P61-67Keywords:
Diabetes, Streptozotocin, Glibenclamide, Wistar Rats, HbA1c, GlutathioneAbstract
Diabetes is a major health issue that has been faced by the majority of the population in the world. Extensive research is being carried out towards development of an antidiabetic component. The aim of the present research was to determine the antidiabetic activity of Corchorus trilocularis Linn plant belonging to the Tiliaceae family. The objectives were to evaluate various serum and pancreatic parameters related to evaluation of diabetes. The whole plant was extracted using various solvents. Phytochemical screening was done for the extracts. Antidiabetic activity was determined using Streptozotocin (STZ) induced diabetes model in rats using 200 mg/kg and 400 mg/kg doses of various extracts. Biochemical components like glycosylated hemoglobin (HbA1c), glutathione, creatine kinase (CK) and lactate dehydrogenase (LDH) were estimated for the collected blood samples from rats. The pancreatic tissue was homogenized and the result was subjected for estimation of TBARS (thiobarbituric acid-reactive substances), catalase, superoxide dismutase (SOD) and glutathione (GSH). Phytochemical screening showed presence of carbohydrates, glycosides, alkaloids, triterpenes, phytosterols, tannins, flavonoids, saponins, mucilage and steroids. The chloroform extract at 400 mg/kg dose significantly lowered the levels of HbA1c and restored blood GSH levels. The levels of CK and LDH were increased in diabetic rats. The treatment with chloroform extract (400 mg/kg) for 21 days significantly reduced the levels of CK when compared to diabetic rats. Extent of TBARS formed was significantly higher (p<0.001) in STZ treated group. In chloroform extract (400 mg/kg) treated groups, TBARS levels have significantly decreased (p<0.001). Diabetic rats treated with chloroform extract (400 mg/kg) showed significant increase (p<0.01) in levels of SOD. GSH activity was reduced in pancreatic tissue of diabetic rats, compared to normal animals. These levels were significantly (p<0.01, p<0.001) increased with chloroform extracts (200 mg/kg and 400 mg/kg) treatment. Thus the present study showed the antidiabetic potency of Corchorus trilocularis Linn plant.
References
Dhanukar SA, Kulkarni RA, Rege NN. Pharmacology of medicinal plants and natural products. Indian J Pharmacol. 2000;32(4):S81-S118.
Kuruvilla A. Herbal formulations as pharmacotherapeutic agents. Indian J Exp Biol. 2002;40(1):7-11. PMID 12561961.
Alam MR, Rahman AB, Moniruzzaman M, Kadir MF, Haque MA, Ratan M. Evaluation of antidiabetic phytochemicals in Syzygium cumini Linn skeels. J Appl Pharm Sci. 2012;2(10):94-8.
Jhansee KD, Mishra A, Kumar DD. Antidiabetic activity and modulation of antioxidant status by Ocimum canum in streptozotocin induced diabetic rats. EurSci J. 2014;10(66):1857-81.
Das SK, Samantaray D, Patra JK, Samanta L, Thatoi H. Antidiabetic potential of mangrove plants: a review. Front Life Sci. 2016;9(1):75-88. doi: 10.1080/21553769.2015.1091386.
Omkar K, Priya K, Anuj A, Gayatri G. Role of herbal interventions in diabetes management. Int J Pharma Bio Sci. 2020;11(1):28-33. doi: 10.22376/ijpbs.2020.11.1.p28-33.
Li WL, Zheng HC, Bukuru J, De Kimpe N. Natural medicines used in the traditional Chinese medical system for therapy of diabetes mellitus. J Ethnopharmacol. 2004;92(1):1-21. doi: 10.1016/j.jep.2003.12.031, PMID 15099842.
Dhanalakshmi R, Manavalan R. Bioactive compounds in leaves of Corchorus trilocularis L. By GC-MS analysis. Int J PharmTech Res. 2014;6(7):1991-8.
Dhanalakshmi R, Manimekalai P. In-vitroantioxidant activities of ethanolic leaf extract of Corchorus trilocularis Linn (Tiliaceae). Int J Chem Pharm Sci. 2018;9(3):48-54.
Khan MSY, Bano S, Javad K, Asad MM. A comprehensive review on the chemistry and pharmacology of Corchorus species – A source of cardiac glycosides, triterpenoids, flavonoids, coumarins, steroids and some other compounds. J SciInd Res. 2006;65(4):283-98.
Kotha P, Badri KR, Nagalapuram R, Allagadda R, Chippada AR. Anti-diabetic potential of the leaves of Anisomeles malabarica in streptozotocin induced diabetic rats. Cell Physiol Biochem. 2017;43(4):1689-702. doi: 10.1159/000484030, PMID 29045936.
Shakira FS, Mohammed M. Experimental evaluation of Antidiabetic effect of Punica granatum peel extract against streptozotocin induced diabetes in albino rats. Int J Pharm Biol Sci. 2020;11(4):115-21.
Ulaganathan I, Nappinnai M, Shanmugapandiyan P. Anti-inflammatory and in-vitro antioxidant potential of extracts leaves of Luffa acutangula in rodent model (rats). Int J Pharm Pharm Sci. 2013;5(2):79-83.
Dibyajyoti S, Bindu J, Vibhor KJ. Phytochemical evaluation and characterization of hypoglycemic activity of various extracts of Abelmoschus esculentus Linn. Int J Pharm Pharm Sci. 2011;3(2):183-5.
OECD. Guidance document on acute oral toxicity 423. Environmental Health and Safety monograph series on testing assessment. Vol. 24; 2000.
Pushpendra K, Gupta PS. Antidiabetic evaluation of various polar and nonpolar extracts of Corchorus trilocularis Linn in streptozotocin induced diabetic animals. Int J Pharm Biol Sci. 2017;7(3):222-8.
Pawan KG, Sandeep J, Kaushik A. Evaluation of antidiabetic activity of Corchorus trilocularis leaves in streptozotocin induced diabetic rats. Int J Pharm Sci Res. 2017;8(7):3075-80.
Anitha T, Balakumar C, Ilango KB, Jose CB, Vetrivel D. Antidiabetic activity of the aqueous extracts of Foeniculum vulgare on streptozotocin induced diabetic rats. Int J Adv Pharm Biol Chem. 2014;3(2):487-94.
Jolinom M, Huguette A, Florence N, Stephane P, Theophile D. Antidiabetic activity of the aqueous extracts of Sarcocephalus pobeguinii (barks) and Nauclea diderichii (leaves and barks) in normal and streptozotocin induced hyperglycemic rats. Int J Adv Res. 2017;5(6):974-82. doi: 10.21474/IJAR01/4499.
18, Ames BN, Shigenaga MK, Hagen TM. Oxidants, antioxidants and the degenerative diseases of aging (cancer or mutation or endogenous DNA adducts or oxygen radicals). Proc Natl Acad Sci U S A. 1993;90(17):7915-22.
Ahmed I, Lakhani MS, Gillett M, John A, Raza H. Hypotriglyceridemic and hypocholesterolemic effects of anti-diabetic Momordica charantia (karela) fruit extract in streptozotocin-induced diabetic rats. Diabetes Res Clin Pract. 2001;51(3):155-61. doi: 10.1016/s0168-8227(00)00224-2, PMID 11269887.
Chen H, Feng R, Guo Y, Sun L, Jiang J. Hypoglycemic effects of aqueous extract of Rhizoma polygonatiodorati in mice and rats. J Ethnopharmacol. 2001;74(3):225-9. doi: 10.1016/s0378-8741(00)00359-7, PMID 11274822.
Dimo T, Ngueguim FT, Kamtchouing P, Dongo E, Tan PV. Glucose lowering efficacy of the aqueous stem bark extract of Trema orientalis (Linn) Blume in normal and streptozotocin diabetic rats. Pharmazie. 2016;61(3):233-6.
Gomathi D, Ravikumar G, Kalaiselvi M, Devaki K, Uma C. Effect of Evolvulus alsinoides on lipid metabolism of streptozotocin induced diabetic rats. Asian Pac J Trop Dis. 2013;3(3):184-8. doi: 10.1016/S2222-1808(13)60037-7.
Jayaprasad B, Sharavanan PS, Sivaraj R. Antidiabetic effect of Chloroxylon swietenia bark extracts on streptozotocin induced diabetic rats. BeniSuef Univ J Basic Appl Sci. 2016;5:61-9.
Shinu P, Parminder N, Mohamed AM, Jaspreet K, Sandhya J, Anroop BN. Mechanisms of antidiabetic activity of methanolic extract of Punica granatum leaves in nicotinamide/streptozotocin induced type 2 diabetes in rats. Plants. 2020;9:1-15.
Morsy MA, Abdel-Aziz AM, Abdel-Hafez SMN, Venugopala KN, Nair AB, Abdel-Gaber SA. The Possible Contribution of P-Glycoprotein in the Protective Effect of Paeonol against Methotrexate-Induced Testicular Injury in Rats. Pharmaceuticals (Basel). 2020;13(9):223. doi: 10.3390/ph13090223, PMID 32872504.
Al-Attar AM, Alsalmi FA. Effect of Olea europaea leaves extract on streptozotocin induced diabetes in male albino rats. Saudi J Biol Sci. 2019;26(1):118-28. doi: 10.1016/j.sjbs.2017.03.002, PMID 30622415.
Khogare DT, Lokhande SM. Effect of Tulsi [Ocimum sanctum] on diabetes mellitus. Indian Stream Research [journal]. 2011;1(2):189-91.
Lutfun N, Sohanur M, Mahadi H. Hypoglycemic and hypolipidemic potential of Nigella sativa Linn seed. Extract in streptozotocin (STZ) induced diabetic rats. J Plant Biochem Physiol. 2015;3(4):2329-36.
Panda SP, Haldar PK, Bera S, Adhikary S, Kandar CC. Antidiabetic and antioxidant activity of Swietenia mahagoni in streptozotocin-induced diabetic rats. Pharm Biol. 2010;48(9):974-9. doi: 10.3109/13880200903390051, PMID 20731547.
Singh R, Bhardwaj P, Sharma P. Antioxidant and toxicological evaluation of Cassia sophera in streptozotocin-induced diabetic Wistar rats. Pharmacognosy Res. 2013;5(4):225-32. doi: 10.4103/0974-8490.118767, PMID 24174814.
Devi M, Komal S, Logeshwari B. Preliminary Phytochemistry and antidiabetic activity of Portulaca grandiflora hook plant extract on streptozotocin induced diabetes in rats. Asian J Pharm Clin Res. 2019;12(12):87-90. doi: 10.22159/ajpcr.2019.v12i12.35216.
Parvin S, Marzan M, Rahman S. Preliminary Phytochemical screening, antihyperglycemic, analgesic and toxicity studies of methanolic extract of aerial parts of Corchorus olitorius Linn. J Appl Pharm Sci. 2015;5(9):68-71.
Sharma AK, Gupta R. Anti-hyperglycemic activity of aqueous extracts of some medicinal plants on Wistar rats. J Diabetes Metab. 2017;08(7):234-40. doi: 10.4172/2155-6156.1000752.
Badole SL, Bodhankar SL, Thakurdesai PA. Study of interaction of aqueous extract of Pleurotus pulmonarius (Fr.) Quel-champ with rosiglitazone in alloxan induced diabetic mice. Pharmacol Online. 2006;3:64-72.
Published
How to Cite
Issue
Section
Copyright (c) 2022 Shaista Omer, Suryadevara Vidyadhara, Doppalapudi Sandeep

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

