"EVALUATION OF NEPHRO PROTECTIVE EFFECT OF NICORANDIL IN STREPTOZOTOCIN-INDUCED NEPHROPATHY IN DIABETIC RATS”

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Yogesh H S
Ranjitha C
Seema Gupta
K. S. Srilatha
S C Marapur

Abstract

BACKGROUND: One of the main microvascular complications of diabetes that leads to end-stage renal disease and the need for kidney dialysis or transplantation is diabetic nephropathy. Neither the kidney damage caused by diabetic nephropathy nor its prevention can be reversed with medication. The goal of the current study was to assess nicorandil's impact on diabetic rats' nephropathy caused by streptozotocin (STZ).


METHOD: Male Wistar rats that had fasted for the whole night were given 50 mg/kg intraperitoneally (i.p.) of streptozotocin to induce diabetes. Rats with fasting blood glucose levels more than 250 mg/dl were classified as diabetics and placed into four groups following a 48-hour streptozotocin treatment. The first two groups were maintained as controls for diabetes and normal conditions, respectively. After inducing diabetes, treatment groups received oral doses of nicorandil (2.5 and 5 mg/kg). These doses were given for six weeks. Serum glucose, glycosylated haemoglobin, serum albumin, serum creatinine, serum total protein, serum blood urea nitrogen, urine albumin, urine creatinine excretion rate, creatinine clearance, kidney index, antioxidant levels in kidney homogenate, MDA levels, and renal histopathology were measured at the conclusion of the six-week Nicorandil treatment.


RESULTS: When compared to the diabetic control group, the insulin-treated diabetic rats exhibited lower serum glucose and glycosylated haemoglobin levels. When compared to diabetic rats, the diabetic treatment rats demonstrated a significant decrease in blood urea nitrogen, serum creatinine, urinary albumin, haemoglobin, kidney index, and increased levels of catalase, superoxide dismutase, glutathione, nitric oxide, and malondialdehyde. Diabetic treatment rats also demonstrated a significant increase in body weight, serum albumin, creatinine clearance, serum total proteins, and urinary creatinine. The kidney's histopathological results provided additional evidence for the preventive role of nitric oxide supplementation in reducing renal damage.


CONCLUSION: Nicorandil demonstrates good effect of renal protection in diabetic rats and so can be a promising drug for treatment and prevention of diabetic nephropathy.

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How to Cite
Yogesh H S, Ranjitha C, Seema Gupta, K. S. Srilatha, & S C Marapur. (2021). "EVALUATION OF NEPHRO PROTECTIVE EFFECT OF NICORANDIL IN STREPTOZOTOCIN-INDUCED NEPHROPATHY IN DIABETIC RATS”. Journal of Advanced Zoology, 42(02), 267–280. https://doi.org/10.53555/jaz.v42i02.4542
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Articles
Author Biographies

Yogesh H S

NITTE College of Pharmaceutical Sciences, Bengaluru, Karnataka, India.

Ranjitha C

Al-Ameen College of Pharmacy Bengaluru, Karnataka, India.

Seema Gupta

Mallige College of Pharmacy Bengaluru, Karnataka, India.

K. S. Srilatha

R.R.College of Pharmacy, Chikkabanavara, Bengaluru, Karnataka, India.

S C Marapur

BLDEA’S SSM college of Pharmacy and Research Centre Vijayapura Karnataka, India

References

Devasenan D, Edwin L, George SE. Type 1 diabetes: recent developments. BMJ.

;328(7442):750-754.

Jahromi MM, Eisenbarth GS. Cellular and molecular pathogenesis of type 1A diabetes.

Cell. Mol. Life. 2007;64(7–8):865–872.

Drummond K, Mauer, M. The early natural history of nephropathy in type 1 diabetes: II. Early renal structural changes in type 1 diabetes. Diabetes.2002; 51(5) : 1580–1587.

Kaur N., Kishore L., Singh R. Diabetic autonomic neuropathy: Pathogenesis to pharmacological management. J DM .2014; 5: 402.

Schena F.P , Gesualdo L. Pathogenetic mechanisms of diabetic nephropathy. J Am Soc Nephrol. 2005 : 30-33.

Tanios B.Y, . Ziyadeh F.N. Emerging therapies for diabetic nephropathy patients: beyond blockade of the renin-angiotensin system . Nephron Extra. 2012 : 278-282

Horie K, Miyata T, Maeda K, Miyata S, Sugiyama S, Sakai H et al. Immunohistochemical colocalization of glycoxidation products and lipid peroxidation products in diabetic renal glomerular lesions. Implication for glycoxidative stress in the pathogenesis of diabetic nephropathy. J Clin Invest. 1997;100:2995-3004.

Taira N. Similarity and dissimilarity in the mode and mechanism of action between nicorandil and classical nitrates: an overview. J Cardiovasc Pharmacol .1987;10:1–9.

Yokota M, Horisawa T, Iwase M, Miyahara T, Yoshida J, Kamihara S . et al. Effects of a new vasodilator, nicorandil, on exercise induced impairment of left ventricular function in patients with old myocardial infarction. J Cardiovasc Pharmacol 1987; 10 ( 8):116– 122.

Jang H. J. Safety and efficacy of a novel hyperaemic agent, intracoronary nicorandil, for invasive physiological assessments in the cardiac catheterization laboratory. Eur Heart J. 2013;34 :2055.

Stracke H, Gaus W, Achenbach K, Ederlin F, Bretzel R.G. Benfotiamine in diabetic poly- nephropathy (bendip): results of a randomised, double blind. Placebo contro clinic study. 2002:1-3

Mano T, Shinohara R., Nagasaka A., Nakagawa H., Uchimura K., Hayashi R., Scavenging effect of nicorandil on free radicals and lipid peroxide in streptozotocin- induced diabetic rats, Metabolism. 2000: 427–431.

Nair and Jacob, A simple practice guide for dose conversion between animals and human, Journal of Basic and Clinical Pharmacy, 2016; 35:866–872.

Kaplan L.A., carbohydrates and metabolites, In Clinical chemistry:Theory,Analysis and co-relation, Kaplan L.A.,and Pesce A.J., Eds.C.V.Mosby,Toronto,1984;1032-1040.

Nathan ,D.M., etal., New Eng.J Med. 1984 : 341- 346.

Gomall, A.;J.Biol.Chem.1949:751

Kishore L, Kour N , Singh R. Nephroprotective effect of Paeonia emodi via inhibition of advanced glycation end products and oxidative stress in STZ- nicotinamide induced diabetic nephropathy. JFDA.2017:576- 588.

Borgohaina M.P, Chowdhurya L, Ahmeda S , Bolshettec N , Devasanid K , Dasa T.J , et al. Renoprotective and antioxidative effects of methanolic Paederia foetida leaf extract on experimental diabetic nephropathy in rats. J. Ethnopharmacol . 2017: 451–459.