IN VITRO AND IN VIVO ANTIHYPERGLYCEMIC EFFECT OF ACTIVE FRACTION OF CLEOME RUTIDOSPERMA DC

Authors

  • I. O. Okoro Department of Biochemistry, Faculty of Science, Delta State University, Abraka
  • I. A. Umar Department of Biochemistry, Ahmadu Bello University, Samaru – Zaria, Nigeria
  • S. E Atawodi Department of Biochemistry, Ahmadu Bello University, Samaru – Zaria, Nigeria
  • K. M. Anigo Department of Biochemistry, Ahmadu Bello University, Samaru – Zaria, Nigeria

Keywords:

Alpha amylase, Alpha glucosidase, C rutidosperma, Glucose 6-phosphatase, Glucose Tolerance, Hypoglycemia, Nil

Abstract

Objective: The present study was aimed to investigate the possible mechanism of action of the active sub fraction of C. rutidosperma. This was done by in vivo and in vitro method.

Methods: Aqueous extract of C. rutidosperma was sequentially fractionated and re-fractionated to yield the active sub fraction (based on in vivo evaluation). In the in vivo study, the active sub fraction was administered to streptozotocin-induced diabetic mice at graded doses in different prandial states; while for the in vitro method, assessment of the possible effects of the active sub fraction of the plant on glucose absorption by excised ileum as well as its effect on α-glucosidase, α-amylase and glucose 6 phosphatase activities was evaluated.

Results: There was significant reduction of blood glucose level by the active sub fraction at different prandial states. The active sub fraction produced comparable hypoglycemic effects as glibenclamide. Likewise, at the doses of 125 and 62.5 mg/kg b. w., it significantly (p<0.05) reduced postprandial hyperglycemia after administration. Glucose tolerance was significantly (p<0.05) improved in the presence of the active sub fraction to varying degrees. The active sub fraction of C. rutidosperma did not demonstrate inhibitory effects on glucose movement into external solution across the rats excised ileum except at 50g/L and 25g/L where a significant (p<0.05) inhibition of glucose movement was observed. Alpha-amylase inhibitory activity of the active sub fraction was found to be 22. 24% at the lowest concentration of 2.50 mg/ml while the highest concentration of 20.00 mg/ml gave 46.66% inhibition. On the other hand, acarbose (standard) showed inhibition of 16.00 % and 34.43% for its lowest and highest concentrations for α-amylase respectively. Similarly, the α-glucosidase inhibitory activity results were: 16.42% and 44.56% for C. rutidosperma and acarbose respectively for the lowest concentration of 2.50 mg/ml, while the highest concentration of 20mg/ml had 64.22% and 87.09% for C. rutidosperma and acarbose respectively. Also, the active sub fraction of the plant showed significant inhibitory activity against glucose 6-phosphatase in a dose dependent fashion.

Conclusions: The results revealed that the possible antihyperglycemic mechanism of action of the plant may be by reduction of postprandial hyperglycemia and improvement of glucose tolerance activity by stimulation of insulin secretion from pancreatic cell and inhibition of carbohydrate hydrolysing enzymes. Consequently, C. rutidosperma may be used as a dietary adjunct to counter hyperglycemia and it has the potential to be developed as new oral antidiabetic agent for the treatment of diabetes mellitus.

 

Downloads

Download data is not yet available.

References

Sharma VK, Kumar S, Patel HJ, Hugar S. Hypoglycemic activity of Ficus glomerata in alloxan induced diabetic rats. Int J Pharm Sci Rev Res 2010;1:18-22.

Altan VM. The pharmacology of diabetic complications. Curr Med Chem 2003;10:1317–27.

Strojek K. Features of macrovascular complications in type 2 diabetic patients. Acta Diabetol 2003;76:269-77.

Shim U, Lee H, Oh JY, Sung YA. Sleep disorder and cardiovascular risk factors among patients with type 2 diabetes mellitus. Korean J Int Med 2011;26:277-84.

Chitra V, Varma CHH, Raju MVRK, Prakash KJ. Study of antidiabetic and free radical scavenging activity of the seed extract of Strychnos nuxvomica. Int J Pharm Pharm Sci 2010;2:106-10.

Atmakuri LR, Dathi S. Current trends in herbal medicines. J Pharm Res 2010;3:109-13.

Malviya N, Jain S, Malviya S. Antidiabetic potential of medicinal plants. Acta Poloniae Pharm-Drug Res 2010;67(2):113-8.

Shrestha S, Yadav S, Mandal F, Amatya M, Islam MN. Prevalence of diabetes mellitus on male and female patient of different age group on hospital based data of chitwan medical college teaching hospital. J Biomed Pharm Res 2013;2(4):66-70.

Ozougwu JC. Anti-diabetic effects of Allium cepa (onions) aqueous extracts on alloxan-induced diabetic Rattus novergicus. Pharmacol Online 2011;1:270–81.

Gnangoran BN, N’guessan BB, Amoateng P, Dosso K, Yapo AP, Ehile EE. Hypoglycaemic activity of ethanolic leaf extract and fractions of Holarrhena floribunda (Apocynaceae). J Med Biomed Sci 2012;1(3):46–54.

Jelodar G, Maleki M, Sirus S. Effect of walnut leaf, coriader and pomegranate on blood glucose and histopathology of pancreas of alloxan induced diabetic rats. Afr J Tradit Complement Altern Med 2007;4:299–305.

Waterhouse B, Mitchell A. Northern Australia Quarantine Strategy Weeds Target List. AQIS Miscellaneous Publication, Canberra; 1998. p. 29.

Bidla G, Titanji VPK, Joko B, El-Ghazali G, Bolad A, Berzins K. Antiplasmodial activity of seven plants used in African folk medicine. Indian J Pharmacol 2004;36(4):245-6.

Bose A, Saravanan VS, Karunanidhi N. Analgesic and locomotor activity of extracts of cleome rutidosperma DC. Indian J Pharm Sci 2004;66:795-7.

Bose A, Gupta JK, Ghosh T. Antimicrobial activity of certain extracts of Cleome rutidosperma. Indian J Nat Prod Resour 2005;21:39-41.

Bose AS, Mondal J, Gupta K, Dash GK, Ghosh T, Si S. Studies on diuretic and laxative activity of ethanol extract and its fractions of Cleome rutidosperma aerial parts. Pharmacogn Mag 2006;2(7):178-82.

Bose A, Gupta JK, Dash GK, Ghosh T, Si S. Diuretic and antibacterial activity of aqueous extract of Cleome rutidosperma. DC Indian J Pharm Sci 2007;69(2):292.

Bose A, Mondal S, Gupta JK. Antioxidant and free radical scavenging activities of Cleome rutidosperma. Oriental Pharm Exp Med 2008;8:135-45.

Bose A, Smith PJ, Lategan CA. Studies on in vitro antiplasmodial activity of Cleome rutidosperma. Acta Polanica Pharm Drug Res 2010;67:315-8.

Burkill HM. The useful plants of west tropical Africa, vol. 1 (Families A-D), 2nd ed. Royal Botanic Gardens, United Kingdom; 1985. p. 960.

Mondal S, Dash GK, Acharyya S, Bose A. Singh. Hypoglycaemic activity from the roots of Cleome rutidosperma DC. J Biomed Sci 2009;4(1):64-9.

Okoro IO, Umar IA, Atawodi SE, Anigo KM. Antidiabetic effect of Cleome rutidosperma Dc and Senecio biafrae (Oliv. & Hiern) extracts in streptozotocin-induced diabetic rats. Int J Pharm Sci Res 2014a;5(6):2480-97.

Guidelines for the care and use of laboratory animals. National Academies Press, 500 Fifth Street, NW, Lockbox 285, Washington, DC 20055 2011;800:6240-2.

Okoro IO, Umar IA, Atawodi SE, Anigo KM. Bioassay-guided isolation of the antidiabetic principles in Cleome rutidosperma DC and Senecio biafrae (Oliv. & Hiern). Int J Pharm Pharm Sci 2014b. (In Press)

Gallagher AM, Flatt PR, Duffy G, Abdel-Wahab YHA. The effects of traditional antidiabetic plants on in vitro glucose diffusion. Nutr Res 2003;23:413–24.

Mohammadi S, Montasser KS, Monavar FA. Antidiabetic properties of the ethanolic extract of Rhus coriaria fruits in rats. DARU J Pharm Sci 2010;18(4):270-5.

Adam Z, Ismail A, Khamis S, Mokhtar MH, Hamid M. Antihyperglycemic activity of F. deltoidea ethanolic extract in normal rats. Sains Malaysiana 2011;40(5):489–95.

Baginsky ES, Foa PP, Zak B. Methods of enzymatic analysis. In: Bergmeyer HU, Gawehn K eds, 2nd ed. New York: Academic Press Inc; 1992;2:876-80.

McCue P, Vattem D, Shetty K. Inhibitory effect of clonal oregano extracts against porcine pancreatic amylase in vitro. Asia Pac J Clin Nutr 2004;13:401–8.

Kim YM, Jeong YK, Wang MH, Lee WY, Rhee HI. Inhibitory effects of pine bark extract on alpha-glucosidase activity and postprandial hyperglycemia. Nutr 2005;21:756-61.

Chacko E. Culture and therapy: complementary strategies for the treatment of type-2 diabetes in an urban setting in Kerala, India. Soc Sci Med 2003;56:1087-98.

Shapiro K, Gong WC. Use of herbal products for diabetes by Latinos. J Am Pharm Assoc 2002;42:278-9.

Grover JK, Yadav S, Vats V. Medicinal Plants of India with antidiabetic potential. J Ethnopharmacol 2002;81:81-100.

Rajagopal K, Sasikala K. Antihyperglycaemic and antihyperlipidaemic effects of Nymphaea stellata in alloxan-induced diabetic rats. Singapore Med J 2008;49:137-41.

David MK. Postprandial blood glucose in the management of type II diabetes: The emerging role of incretin mimetics. Medscape: Diabetes Endocrinol 2005;7:2.

Baron AD. Postprandial hyperglycemia and α-glucosidase inhibitors. Diabetes Res Clin Pract 1998;40:S51-S5.

Bhaskar A, Vidhya VG, Ramya M. Hypoglycemic effect of Mucuna pruriens seed extract on normal and streptozotocin-diabetic rats. Fitoterapia 2008;79:539-43.

Nomikos T, Detopoulou P, Fragopoulou E, Pliakis E, Antonopoulou S. Boiled wild artichoke reduces postprandial glycemic and insulinemic responses in normal subjects but has no effect on metabolic syndrome patients. Nutr Res 2007;27(12):741-9.

Venkatesh S, Reddy DG, Reddy YSR, Sathyavathy D, Reddy BM. Effects of Helicteres isora root extract on glucose tolerance in glucose-induced hyperglycemic rats. Fitoterapia 2004;75(3-4):364-7.

Ortiz-Andrade RR, Garc´Ia-Jim´Enez S, Castillo-Espa˜Na P, Ram´Irez-A´Vila G, Villalobos-Molina R, Estrada-Soto S. α-Glucosidase inhibitory activity of the methanolic extract from Tournefortia hartwegiana: an anti-hyperglycemic agent. J Ethnopharmacol 2007;109:48-53.

Dicarli MF, Janisse J, Grunberger G, Ager J. Role of chronic hyperglycemia in the pathogenesis of coronary microvascular dysfunction in diabetes. J Am Coll Cardiol 2003;41:1387–93.

Kimura Y, Araki Y, Takenaka A, Igarashi K. Protective effect of dietary nasunin and parapect induced oxidative stress in rat. Biosci Biotechnol Biochem 2006;63:799-804.

Pinto MDS, Ranilla LG, Apostolidis E, Lajolo FM, Genovese MI, Shetty K. Evaluation of anti-hyperglycemia and antihypertension potential of native Peruvian fruits using in vitro models. J Med Food 2009;12:278-91.

Kwon YI, Apostolidis E, Kim YC, Shetty K. Health benefits of traditional corn, beans and pumpkin; In vitro studies for hyperglycemia and hypertension management. J Med Food 2007;10:266-75.

Dafnis E, Sabatini S. Biochemistry and pathology of vanadium. Nephron 1994;67:133–43.

Domingo JL, Gomez M, Sanchez DJ. Toxicology of vanadium compounds in diabetic rats: the action of chelating agents on vanadium accumulation. Mol Cell Biochem 1995;153:233–40.

Smith C, Marks AD, Lieberman M. Marks’s Basic Medical Biochemistry: A Clinical Approach, 2nd Edition, Lippincott Williams & Wilkins, Baltimore, Maryland; 2005. p. 21201-2436.

Agius L. New hepatic targets for glycemic control in diabetes. Best Practice Res Clin Endocrinol Metab 2007;4:587-605.

Pari L, Satheesh MA. Effects of pterostilbene on hepatic key enzymes of glucose metabolism in streptozotocin and nicotinamide induced diabetic rats. Life Sci 2006;79(7):641-5.

Published

01-01-2015

How to Cite

Okoro, I. O., I. A. Umar, S. E. Atawodi, and K. M. Anigo. “IN VITRO AND IN VIVO ANTIHYPERGLYCEMIC EFFECT OF ACTIVE FRACTION OF CLEOME RUTIDOSPERMA DC”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 1, Jan. 2015, pp. 289-95, https://innovareacademics.in/journals/index.php/ijpps/article/view/3337.

Issue

Section

Original Article(s)