HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Uncoupling protein-2 mediates the protective action of berberine against oxidative stress in rat insulinoma INS-1E cells and in diabetic mouse islets.

AbstractBACKGROUND AND PURPOSE:
Uncoupling protein-2 (UCP2) may regulate glucose-stimulated insulin secretion. The current study investigated the effects of berberine, an alkaloid found in many medicinal plants, on oxidative stress and insulin secretion through restoration of UCP2 expression in high glucose (HG)-treated INS-1E cells and rat islets or in db/db mouse islets.
EXPERIMENTAL APPROACH:
Mouse and rat pancreatic islets were isolated. Nitrotyrosine, superoxide dismutase (SOD)-1 and UCP2 expression and AMPK phosphorylation were examined by Western blotting. Insulin secretion was measured by ELISA. Mitochondrial reactive oxygen species (ROS) production was detected by confocal microscopy.
KEY RESULTS:
Incubation of INS-1E cells and rat islets with HG (30 mmol·L(-1); 8 h) elevated nitrotyrosine level, reduced SOD-1 and UCP2 expression and AMPK phosphorylation, and inhibited glucose-stimulated insulin secretion. HG also increased mitochondrial ROS in INS-1E cells. Co-treatment with berberine inhibited such effects. The AMPK inhibitor compound C, the UCP2 inhibitor genipin and adenovirus ucp2 shRNA inhibited these protective effects of berberine. Furthermore, compound C normalized berberine-stimulated UCP2 expression but genipin did not affect AMPK phosphorylation. Islets from db/db mice exhibited elevated nitrotyrosine levels, reduced expression of SOD-1 and UCP2 and AMPK phosphorylation, and decreased insulin secretion compared with those from db/m(+) mice. Berberine also improved these defects in diabetic islets and genipin blocked the effects of berberine.
CONCLUSIONS AND IMPLICATIONS:
Berberine inhibited oxidative stress and restored insulin secretion in HG-treated INS-IE cells and diabetic mouse islets by activating AMPK and UCP2. UCP2 is an important signalling molecule in mediating anti-diabetic effects of berberine.
AuthorsLimei Liu, Jian Liu, Yuansheng Gao, Xiaoxing Yu, Gang Xu, Yu Huang
JournalBritish journal of pharmacology (Br J Pharmacol) Vol. 171 Issue 13 Pg. 3246-54 (Jul 2014) ISSN: 1476-5381 [Electronic] England
PMID24588674 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 The British Pharmacological Society.
Chemical References
  • Insulin
  • Ion Channels
  • Iridoids
  • Mitochondrial Proteins
  • Reactive Oxygen Species
  • Ucp2 protein, mouse
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • Berberine
  • genipin
  • AMP-Activated Protein Kinases
  • Glucose
Topics
  • AMP-Activated Protein Kinases (metabolism)
  • Animals
  • Berberine (pharmacology)
  • Diabetes Mellitus, Experimental (physiopathology)
  • Glucose (metabolism)
  • Insulin (metabolism)
  • Insulin Secretion
  • Insulinoma (pathology)
  • Ion Channels (metabolism)
  • Iridoids (pharmacology)
  • Islets of Langerhans (drug effects, pathology)
  • Male
  • Mice
  • Microscopy, Confocal
  • Mitochondria (metabolism)
  • Mitochondrial Proteins (metabolism)
  • Oxidative Stress (drug effects)
  • Pancreatic Neoplasms (pathology)
  • Phosphorylation (drug effects)
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species (metabolism)
  • Uncoupling Protein 2

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: