Article

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

Institute of Natural Medicine, University of Toyama, Toyama, Japan.
The Journal of pharmacy and pharmacology 03/2010; 62(3):374-80. DOI:10.1211/jpp.62.03.0013 pp.374-80
Source: PubMed

ABSTRACT The effects of morroniside isolated from Corni Fructus on renal lipids and inflammation provoked by hyperglycaemia were investigated using type 2 diabetic mice.
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.
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.
Morroniside may inhibit abnormal lipid metabolism and inflammation due to reactive oxygen species in the kidneys in type 2 diabetes.

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Keywords

abnormal lipid metabolism
 
abnormal protein expression
 
Corni Fructus
 
db/db mice
 
inducible nitric oxide synthase augmented
 
lipid homeostasis
 
lipid levels
 
lipid peroxidation
 
morroniside alleviated oxidative stress
 
morroniside-treated db/db mouse group
 
nuclear factor-kappaBp65
 
protein expression
 
reactive oxygen species
 
renal biochemical factors
 
renal glucose
 
renal lipids
 
significant dose-dependent reductions
 
type 2 diabetes
 
type 2 diabetic mice
 
vehicle-treated db/db
 

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