HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Evaluation of morroniside, iridoid glycoside from Corni Fructus, on diabetes-induced alterations such as oxidative stress, inflammation, and apoptosis in the liver of type 2 diabetic db/db mice.

Abstract
The present study was conducted to examine whether morroniside has an ameliorative effect on diabetes-induced alterations such as oxidative stress, inflammation, and apoptosis in the liver of type 2 diabetic db/db mice. Morroniside (20 or 100 mg/kg body weight/d, per os (p.o.)) was administered every day for 8 weeks to db/db mice, and its effect was compared with vehicle-treated db/db and m/m mice. The administration of morroniside decreased the elevated serum glucose concentration in db/db mice, and reduced the increased oxidative biomarkers including the generation of reactive oxygen species and lipid peroxidation in the liver. The db/db mice exhibited the up-regulation of nicotinamide adenine dinucleotide phosphate oxidase subunits, NF-E2-related factor 2 (Nrf2), heme oxygenase-1, nuclear factor-kappa B, cyclooxygenase-2, inducible nitric oxide synthase, monocyte chemotactic protein-1, and intracellular adhesion molecule-1 levels in the liver; however, morroniside treatment significantly reduced those expressions. Moreover, the augmented expressions of apoptosis-related proteins, Bax and cytochrome c, were down-regulated by morroniside administration. Hematoxylin-eosin staining showed that the increased hepatocellular damage in the liver of db/db mice improved on morroniside administration. Taking these into consideration, our findings support the therapeutic evidence for morroniside ameliorating the development of diabetic hepatic complications via regulating oxidative stress, inflammation, and apoptosis.
AuthorsChan Hum Park, Jeong Sook Noh, Ji Hyun Kim, Takashi Tanaka, Qi Zhao, Kinzo Matsumoto, Naotoshi Shibahara, Takako Yokozawa
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 34 Issue 10 Pg. 1559-65 ( 2011) ISSN: 1347-5215 [Electronic] Japan
PMID21963495 (Publication Type: Journal Article)
Chemical References
  • Antioxidants
  • Blood Glucose
  • Glycosides
  • Histones
  • Hypoglycemic Agents
  • Iridoid Glycosides
  • NF-E2-Related Factor 2
  • Plant Preparations
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances
  • Transcription Factor RelA
  • morroniside
  • Heme Oxygenase-1
  • Cyclooxygenase 2
Topics
  • Animals
  • Antioxidants (metabolism)
  • Apoptosis (drug effects)
  • Blood Glucose (drug effects)
  • Cornus
  • Cyclooxygenase 2 (metabolism)
  • Diabetes Mellitus, Type 2 (drug therapy, genetics, metabolism, pathology)
  • Drug Evaluation, Preclinical
  • Glycosides (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Heme Oxygenase-1 (metabolism)
  • Histones (analysis, drug effects)
  • Hypoglycemic Agents (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Inflammation (drug therapy)
  • Iridoid Glycosides (chemistry, isolation & purification, pharmacology)
  • Liver (cytology, drug effects, metabolism, physiopathology)
  • Liver Function Tests
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Targeted Therapy
  • NF-E2-Related Factor 2 (drug effects)
  • Oxidative Stress (drug effects)
  • Phytotherapy
  • Plant Preparations (chemistry, isolation & purification, pharmacology)
  • Reactive Oxygen Species (metabolism)
  • Thiobarbituric Acid Reactive Substances (metabolism)
  • Transcription Factor RelA (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: