Abstract | AIM: METHODS:
Trimetazidine was administered to db/db mice for eight weeks. Cardiac function was measured by inserting a Millar catheter into the left ventricle, and oxidative stress and AMP-activated protein kinase (AMPK) activity in the myocardium were evaluated. RESULTS: Untreated db/db mice exhibited a significant decrease in cardiac function compared to normal C57 mice. Oxidative stress and lipid deposition were markedly increased in the myocardium, concomitant with inactivation of AMPK and increased expression of peroxisome proliferator-activated receptor coactivator-1 alpha (PGC-1 alpha). Trimetazidine significantly improved systolic and diastolic function in hearts of db/db mice and led to reduced production of reactive oxygen species and deposition of fatty acid in cardiomyocytes. Trimetazidine also caused AMPK activation and reduced PGC-1 alpha expression in the hearts of db/db mice. CONCLUSION: The data suggest that trimetazidine significantly improves cardiac function in db/db mice by attenuating lipotoxicity and improving the oxidation status of the heart. Activation of AMPK and decreased expression of PGC-1 alpha were involved in this process. Furthermore, our study suggests that trimetazidine suppresses the development of diabetic cardiomyopathy, which warrants further clinical investigation.
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Authors | Yuan-jing Li, Pei-hua Wang, Chen Chen, Ming-hui Zou, Dao-wen Wang |
Journal | Acta pharmacologica Sinica
(Acta Pharmacol Sin)
Vol. 31
Issue 5
Pg. 560-9
(May 2010)
ISSN: 1745-7254 [Electronic] United States |
PMID | 20383170
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antioxidants
- Fats
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
- Ppargc1a protein, mouse
- Reactive Oxygen Species
- Trans-Activators
- Transcription Factors
- Triglycerides
- AMP-Activated Protein Kinases
- Trimetazidine
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Topics |
- AMP-Activated Protein Kinases
(metabolism)
- Animals
- Antioxidants
(pharmacology, therapeutic use)
- Diabetes Complications
(drug therapy)
- Diabetes Mellitus
(metabolism)
- Fats
(analysis, metabolism)
- Heart
(drug effects)
- Lipid Peroxidation
(drug effects)
- Male
- Mice
- Mice, Inbred C57BL
- Myocardium
(metabolism, pathology)
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
- Reactive Oxygen Species
(metabolism)
- Trans-Activators
(metabolism)
- Transcription Factors
- Triglycerides
(blood)
- Trimetazidine
(pharmacology, therapeutic use)
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