Literature DB >> 22116744

Protective effect of herbomineral formulation (Dolabi) on early diabetic nephropathy in streptozotocin-induced diabetic rats.

Mirza A Baig1, Vikas B Gawali, Rajesh R Patil, Suresh R Naik.   

Abstract

The effect of a herbomineral formulation (HMF) on early diabetic nephropathy was investigated. Diabetes was induced in Wistar rats by administering streptozotocin (55 mg/kg, intraperitoneally). The occurrence of early diabetic nephropathy in rats was revealed by high plasma glucose and depleted liver glycogen, decreased glucose uptake by peripheral tissue, impaired renal function, increased antioxidants and lipid peroxidation in kidney. These changes were accompanied by elevated malondialdehyde, glutathione and superoxide dismutase activity in kidney. Furthermore, increased total urine volume, urinary albumin excretion rate, urinary albumin to creatinine ratio, increased relative kidney weight, decreased glomerular filtration rate (GFR) and urinary creatinine were also observed in diabetic nephropathy rats. HMF treatment significantly lowered blood glucose, glycosylated hemoglobin, creatinine, blood urea nitrogen, triglycerides, total cholesterol, serum albumin level, total urine volume, urinary albumin excretion rate, urinary albumin to creatinine ratio and relative kidney weight, and increased urinary creatinine and GFR. Altered levels of antioxidants, viz. lipid peroxidation, glutathione and superoxide dismutase (SOD), in kidney of diabetic nephropathy rats were restored. Histopathological findings indicated dense mesangial matrix in the glomeruli of diabetic nephropathy rats, which may be due to over-activation of matrix metalloproteinases and was reduced following HMF treatment. Our experimental findings clearly demonstrate that HMF has an ability to prevent the progression of early diabetic nephropathy. Such protective effect of HMF might be due to the presence of flavonoids (catechin, quercetin, rutin) and triterpene saponins (oleanolic acid and gymnemic acid) which are known to possess potent antioxidant properties.

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Year:  2011        PMID: 22116744     DOI: 10.1007/s11418-011-0614-y

Source DB:  PubMed          Journal:  J Nat Med        ISSN: 1340-3443            Impact factor:   2.343


  36 in total

1.  Improved method for the determination of blood glutathione.

Authors:  E BEUTLER; O DURON; B M KELLY
Journal:  J Lab Clin Med       Date:  1963-05

2.  Animal model of diabetic nephropathy.

Authors:  T Yokozawa; T Nakagawa; K Wakaki; F Koizumi
Journal:  Exp Toxicol Pathol       Date:  2001-10

3.  Effects of Acacia arabica and Caralluma edulis on blood glucose levels of normal and alloxan diabetic rabbits.

Authors:  A Wadood; N Wadood; S A Shah
Journal:  J Pak Med Assoc       Date:  1989-08       Impact factor: 0.781

Review 4.  Oxidative stress and stress-activated signaling pathways: a unifying hypothesis of type 2 diabetes.

Authors:  Joseph L Evans; Ira D Goldfine; Betty A Maddux; Gerold M Grodsky
Journal:  Endocr Rev       Date:  2002-10       Impact factor: 19.871

5.  Effects of specific antagonists of angiotensin II receptors and captopril on diabetic nephropathy in mice.

Authors:  T Yotsumoto; T Naitoh; K Shikada; S Tanaka
Journal:  Jpn J Pharmacol       Date:  1997-09

Review 6.  Rodent models of streptozotocin-induced diabetic nephropathy.

Authors:  Greg H Tesch; Terri J Allen
Journal:  Nephrology (Carlton)       Date:  2007-06       Impact factor: 2.506

7.  Changes in metabolism of rat kidney and liver caused by experimental diabetes and by dietary sucrose.

Authors:  S S Kang; R Fears; S Noirot; J N Mbanya; J Yudkin
Journal:  Diabetologia       Date:  1982-04       Impact factor: 10.122

Review 8.  Activation of protein kinase C in glomerular cells in diabetes. Mechanisms and potential links to the pathogenesis of diabetic glomerulopathy.

Authors:  F R Derubertis; P A Craven
Journal:  Diabetes       Date:  1994-01       Impact factor: 9.461

9.  Long-term antihypertensive treatment inhibiting progression of diabetic nephropathy.

Authors:  C E Mogensen
Journal:  Br Med J (Clin Res Ed)       Date:  1982-09-11

10.  Effect of chronic treatment with losartan on streptozotocin-induced renal dysfunction.

Authors:  B Murali; Dhananjay N Umrani; Ramesh K Goyal
Journal:  Mol Cell Biochem       Date:  2003-07       Impact factor: 3.396

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