Anti-hyperglycemic activity of rutin in streptozotocin-induced diabetic rats: an effect mediated through cytokines, antioxidants and lipid biomarkers

Indian J Exp Biol. 2014 Jul;52(7):720-7.

Abstract

Administration of rutin (50 and 100 mg/kg) and pioglitazone (10 mg/kg) orally for 3 weeks treatment significantly improved body weight, reduced plasma glucose and glycosylated hemoglobin, pro-inflammatory cytokines (IL-6 and TNF-alpha), restored the depleted liver antioxidant status and serum lipid profile in high fat diet + streptozotocin induced type 2 diabetic rats. Rutin treatment also improved histo-architecture of beta islets and reversed hypertrophy of hepatocytes. Rutin exhibited significant antidiabetic activity, presumably by inhibiting inflammatory cytokines, improving antioxidant and plasma lipid profiles in High fat diet + streptozotocin induced type 2 diabetic model and may be useful as a diabetic modulator along with standard antidiabetic drugs. However, such effects need to be confirmed on human subjects in clinical condition.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Biomarkers / metabolism
  • Blood Glucose / analysis
  • Body Weight / drug effects
  • Diabetes Complications / drug therapy
  • Diabetes Complications / etiology
  • Diabetes Complications / metabolism
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diet, High-Fat / adverse effects
  • Female
  • Glycated Hemoglobin / analysis
  • Hyperglycemia / drug therapy*
  • Hyperglycemia / etiology
  • Hyperglycemia / metabolism
  • Hypoglycemic Agents / pharmacology
  • Insulin / metabolism
  • Insulin-Secreting Cells / metabolism
  • Interleukin-6 / metabolism*
  • Lipids / blood*
  • Male
  • Mice
  • Pioglitazone
  • Rats, Sprague-Dawley
  • Rutin / pharmacology*
  • Thiazolidinediones / pharmacology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Antioxidants
  • Biomarkers
  • Blood Glucose
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Insulin
  • Interleukin-6
  • Lipids
  • Thiazolidinediones
  • Tumor Necrosis Factor-alpha
  • Rutin
  • Pioglitazone