Effects of morroniside isolated from Corni Fructus on renal lipids and inflammation in type 2 diabetic mice

J Pharm Pharmacol. 2010 Mar;62(3):374-80. doi: 10.1211/jpp.62.03.0013.

Abstract

Objectives: The effects of morroniside isolated from Corni Fructus on renal lipids and inflammation provoked by hyperglycaemia were investigated using type 2 diabetic mice.

Methods: Morroniside was administered orally to db/db mice at 20 or 100 mg/kg daily for 8 weeks, and its effects were compared with those in vehicle-treated db/db and m/m (non-diabetic) mice. Serum and renal biochemical factors and protein expression related to lipid homeostasis and inflammation were measured.

Key findings: Morroniside produced significant dose-dependent reductions in serum triglyceride and renal glucose and lipid levels. Morroniside altered the abnormal protein expression of sterol regulatory element binding proteins (SREBP-1 and SREBP-2). In addition, the formation of reactive oxygen species and lipid peroxidation were inhibited in the morroniside-treated db/db mouse group, and the ratio of reduced glutathione to the oxidised form was significantly elevated. These results suggest that morroniside alleviated oxidative stress in the kidneys of db/db mice. Furthermore, 100 mg/kg morroniside down-regulated the expression of nuclear factor-kappaBp65, cyclooxygenase-2 and inducible nitric oxide synthase augmented in db/db mice.

Conclusions: Morroniside may inhibit abnormal lipid metabolism and inflammation due to reactive oxygen species in the kidneys in type 2 diabetes.

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cornus / chemistry*
  • Cyclooxygenase 2 / metabolism
  • Diabetes Mellitus, Experimental
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetic Nephropathies / metabolism*
  • Dose-Response Relationship, Drug
  • Fruit / chemistry*
  • Glucose / metabolism
  • Glycosides / therapeutic use*
  • Inflammation / etiology
  • Inflammation / metabolism*
  • Lipid Metabolism / drug effects*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide Synthase Type I / metabolism
  • Oxidative Stress / drug effects
  • Plants, Medicinal / chemistry
  • Sterol Regulatory Element Binding Proteins / metabolism
  • Transcription Factor RelA / metabolism
  • Triglycerides / blood

Substances

  • Biomarkers
  • Glycosides
  • Sterol Regulatory Element Binding Proteins
  • Transcription Factor RelA
  • Triglycerides
  • morroniside
  • Nitric Oxide Synthase Type I
  • Nos1 protein, mouse
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Glucose