Research Journal of Pharmacy and Technology
SCOPUS
  • Year: 2024
  • Volume: 17
  • Issue: 10

Hypoglycemia and hypolipidemia assisted nephroprotective potential of Hygrophila auriculata (K. Schum) heine in streptozotocin/nicotinamide rodent model of type 2 diabetes

  • Author:
  • Vishal B. Jadhav1,2,*, Yogesh S. Ahire3, Chandrashekhar D. Patil4, Jai Singh Vaghela2
  • Total Page Count: 7
  • Page Number: 4873 to 4879

1Department of Pharmacology, GES's Sir Dr. M. S. Gosavi College of Pharmaceutical Education and Research, Nashik - 422005, Maharashtra, India

2Department of Pharmacology, Bhupal Nobles’ College of Pharmacy, Bhupal Nobles’ University, Udaipur - 313001, Rajasthan, India

3Department of Pharmacology, K.B.H.S.S. Trust's Institute of Pharmacy, Malegaon, Nashik - 423501, Maharashtra, India

4Department of Pharmacology, Divine College of Pharmacy, Satana, Nashik - 423101, Maharashtra, India

*Corresponding Author E-mail: kavyashri9312@yahoo.com

Online published on 6 May, 2025.

Abstract

The investigation was aimed at testing the nephroprotective potential of methanol extract (MEHA) from Hygrophila auriculata (K. Schum) Heine against hyperglycemia and dyslipidemia in adult Wistar albino rats with streptozotocin (STZ)/ nicotinamide (NA)-induced diabetic kidney disease (DKD). Adult male albino Wistar rats with fasting blood glucose (FBG) levels greater than 250 mg/dL were selected and randomly assigned to six groups after the induction of diabetes. The normoglycemic group (Group I) received oral saline, while diabetic groups (II-VI) received saline, MEHA at doses of 100, 200, and 400 mg/kg, and metformin (MET) at 180 mg/kg, respectively. MEHA and MET were administered orally as a 1% carboxymethyl cellulose (CMC) suspension from the 5th to the 8th week after diabetes induction. At week 8, comprehensive assessments were conducted to evaluate renal function, glycemic control, dyslipidemia, oxidative stress markers, and kidney histoarchitecture. MEHA treatment at 200 and 400 mg/kg and metformin demonstrated significant reductions in hyperglycemia, dyslipidemia, and oxidative stress. Furthermore, improved renal function indices and reduced vacuolar degeneration in renal tubules was seen in diabetic rats following MEHA and MET administration. The present study provides compelling evidence for the renoprotective efficacy of MEHA against STZ/NA-induced DKD in rats. This effect is likely attributed to MEHA's hypoglycemic, hypolipidemic, and antioxidant properties.

Keywords

Diabetic kidney disease, Hyperglycemia, Dyslipidemia, Oxidative stress, Antioxidant