Pancreato-protective PANCREATOPROTECTIVE EFFECT OF SILYMARIN ON OXIDATIVE STRESS IN ALLOXAN-INDUCED HYPERGLYCEMIA IN MALE WISTAR RATS

Authors

  • UMA NARAYANAMURTHY Department of Pharmacology, Mahatma Gandhi Medical College and Research Institute, SBV University, Pillaiyarkuppam, Puducherry, India.
  • SYLVIA SANTHAKUMARI A Division of Pharmacology, Rajah Muthiah Medical College Hospital, Annamalai University, Chidambaram, Tamil Nadu, India.
  • NIRMALA P Division of Pharmacology, Rajah Muthiah Medical College Hospital, Annamalai University, Chidambaram, Tamil Nadu, India.

DOI:

https://doi.org/10.22159/ajpcr.2019.v12i10.34482

Keywords:

Diabetes, Oxidative stress, Pancreas, Silymarin

Abstract

Objective: The objective of the study was to study the silymarin’s pancreatoprotective effect in alloxan-induced Type I diabetes mellitus. Numerous studies have evidence to prove the fact that antioxidant defense mechanism of flavonoids has overcome the progression of chronic diabetic complications.

Methods: A total of 24 male Wistar rats were divided into four groups (n=6): Group I normal control, Group II, Group III, and Group IV were induced diabetes with alloxan. Group I and Group II diabetic rats received the vehicle (PO). Group III was treated with silymarin 400 mg/kg (PO). Group IV was treated with glibenclamide 0.5 mg/kg, per orally for 21 days. Fasting blood samples were collected from all four groups of animals at the end of 21 days to evaluate serum glucose and glycosylated hemoglobin (HbA1c). Pancreatic tissue extraction, to perform lipid peroxidation and histopathological study confirms the level of oxidative damage to tissues and recovery after treatment.

Results: The serum glucose and HbA1c levels significantly increased in untreated diabetic rats, also a significant rise in lipid peroxidation and necrosis of beta cells in the pancreatic tissue. The rise in serum glucose levels was ameliorated in rats treated with silymarin, pancreatic tissue showed increased antioxidant levels, decreased lipid peroxides, and minimal changes and signs of regeneration of beta cells.

Conclusion: This study adds experimental evidence to the fact that silymarin is an effective nutritional supplement to treasure pancreatic beta-cell reserve and to delay diabetic complications.

Downloads

Download data is not yet available.

Author Biographies

SYLVIA SANTHAKUMARI A, Division of Pharmacology, Rajah Muthiah Medical College Hospital, Annamalai University, Chidambaram, Tamil Nadu, India.

Department of Pharmacology, Professor

NIRMALA P, Division of Pharmacology, Rajah Muthiah Medical College Hospital, Annamalai University, Chidambaram, Tamil Nadu, India.

Department of Pharmacology, Professor and Head

References

Triplitt CL, Reasner CA. Diabetes mellitus. In: Dipiro JT, Talbert RL, Yee GC, Matzke GR, Wells BW, Posey LM, editors. Pharmacotherapy A Pathophysiologic Approach. 8th ed., Vol. 83. China: McGraw-Hill Companies; 2011. p. 1255-302.

Martin NM, Bloom SR. Pancreatic endocrine disorders and multiple endocrine neoplasia. In: Warell DA, Cox TM, Firth JD, editors. Oxford Textbook of Medicine. 5th ed., Vol. 13. New York: Oxford University Press; 2010. p. 1976-86.

Powers AC. Diabetes mellitus. In: Kasper DL, Faver AS, Longo DL, Branunald E, Hauser SC, Janesen JL, editors. Harrison’s Principles of Internal Medicine. 16th ed., Vol. 323. New York: McGraw-Hill Book Co.; 2005. p. 2152-62.

Ahmadvand H. Effects of coenzyme Q10 on hemoglobin A1C, serum urea and creatinine in alloxan-induced Type 1 diabetic rat. Iran J Pharmacol Ther 2012;11:64-7.

Morazzoni P, Bombardelli E. Silybum marianum (Carduus marianus). Fitoterapia 1995;64:3-42.

Tokuyama Y, Sturis J, DePaoli AM, Takeda J, Stoffel M, Tang J, et al. Evolution of beta-cell dysfunction in the male zucker diabetic fatty rat. Diabetes 1995;44:1447-57.

Rudich A, Tirosh A, Potashnik R, Hemi R, Kanety H, Bashan N, et al. Prolonged oxidative stress impairs insulin-induced GLUT4 translocation in 3T3-L1 adipocytes. Diabetes 1998;47:1562-9.

Kaneto H, Fujii J, Myint T, Miyazawa N, Islam KN, Kawasaki Y, et al. Reducing sugars trigger oxidative modification and apoptosis in pancreatic beta-cells by provoking oxidative stress through the glycation reaction. Biochem J 1996;320 (Pt 3):855-63.

Stahl W, Sies H. Antioxidant defense: Vitamins E and C and carotenoids. Diabetes 1997;46 Suppl 2:S14-8.

Ross JA, Kasum CM. Dietary flavonoids: Bioavailability, metabolic effects, and safety. Annu Rev Nutr 2002;22:19-34.

Simanek V, Kren V, Ulrichova J, Vicar J, Cvak L. Silymarin: What is in the name? Hepatology 2000;32:442-3.

Magliulo E, Carosi PG, Minoli L, Gorini S. Studies on the regenerative capacity of the liver in rats subjected to partial hepatectomy and treated with silymarin. Arzneimittelforschung 1973;23:161-7.

Dehmlow C, Erhard J, de Groot H. Inhibition of kupffer cell functions as an explanation for the hepatoprotective properties of silibinin. Hepatology 1996;23:749-54.

Kren V, Walterová D. Silybin and silymarin new effects and applications. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2005;149:29-41.

Sonnenbichler J, Zetl I. Biochemical effects of the flavonolignane silibinin on RNA, protein and DNA synthesis in rat livers. Prog Clin Biol Res 1986;213:319-31.

Dehmlow C, Murawski N, de Groot H. Scavenging of reactive oxygen species and inhibition of arachidonic acid metabolism by silibinin in human cells. Life Sci 1996;58:1591-600.

Saliou C, Rihn B, Cillard J, Okamoto T, Packer L. Selective inhibition of NF-kappaB activation by the flavonoid hepatoprotector silymarin in hepG2. Evidence for different activating pathways. FEBS Lett 1998;440:8-12.

Lal VK, Gupta PP, Awanish P. Hypoglycemic effect of kyllinga triceps in STZ induced diabetic rats. J Diabetes Metab 2012;3:6.

Sangeetha C, Saxena RC, Chaurasia ID, Shrivastav R. Antidiabetic activity of Luffer aegyptica (Mill) in alloxan induced diabetic rats. J Chem Pharm Res 2011;3:522-5.

Rao BK, Kesavulu MM, Giri R, Appa Rao C. Antidiabetic and hypolipidemic effects of Momordica cymbalaria hook. Fruit powder in alloxan-diabetic rats. J Ethnopharmacol 1999;67:103-9.

Medhi B, Prakash P. Introduction to experimental pharmacology (I) blood collection from the experimental animals. In: Practical Manual of Experimental and Clinical Pharmacology. 1st ed., Vol. 1. New Delhi: Jaypee Brothers Medical Publishers (P) Ltd.; 2010. p. 30-3.

Medhi B, Prakash A. Introduction to experimental pharmacology (M) anesthesia and experimental animals. In: Practical Manual of Experimental and Clinical Pharmacology. 1st ed., Vol. 1. New Delhi: Jaypee Brothers Medical Publishers (P) Ltd.; 2010. p. 37-9.

International Diabetes Federation. Epidemiology Global Status. In Diabetes Atlas 21st Century. Brussels: IDF Executive Office; 2013.

Rohilla A, Ali S. Alloxan induced diabetes: Mechanisms and effects. Int J Res Pharm Biomed Sci 2012;3:819-23.

Silybum marianum (milk thistle). Altern Med Rev 1999;4:272-4.

Soto C, Recoba R, Barrón H, Alvarez C, Favari L. Silymarin increases antioxidant enzymes in alloxan-induced diabetes in rat pancreas. Comp Biochem Physiol C Toxicol Pharmacol 2003;136:205-12.

Al-Enazi MM. Combined therapy of rutin and silymarin has more protective effects on STZ-induced oxidative stress in rats. J Appl Pharma Sci 2014;4:21-8.

Bagri P, Ali M, Aeri V, Bhowmik M. Isolation and antidiabetic activity of new lanostenoids from the leaves of Psidium guajava L. Int J Pharm Pharm Sci 2016;8:14-8.

El Kabbaoui M, Chda A, Mejrhit N, Farah A, Aarab L, Bencheikh R, et al. Antidiabetic effect of Thymus satureioides aqueous extract in STZ-induced diabetic rats. Int J Pharm Pharm Sci 2016;8:140-5.

Published

07-10-2019

How to Cite

UMA NARAYANAMURTHY, SYLVIA SANTHAKUMARI A, and NIRMALA P. “Pancreato-Protective PANCREATOPROTECTIVE EFFECT OF SILYMARIN ON OXIDATIVE STRESS IN ALLOXAN-INDUCED HYPERGLYCEMIA IN MALE WISTAR RATS”. Asian Journal of Pharmaceutical and Clinical Research, vol. 12, no. 10, Oct. 2019, pp. 121-5, doi:10.22159/ajpcr.2019.v12i10.34482.

Issue

Section

Original Article(s)