Effect of metformin therapy on cardiac function and survival in a volume-overload model of heart failure in rats
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články
PubMed
21275906
DOI
10.1042/cs20100527
PII: CS20100527
Knihovny.cz E-zdroje
- MeSH
- analýza přežití MeSH
- glykogen metabolismus MeSH
- hemodynamika účinky léků MeSH
- hypoglykemika krev terapeutické užití MeSH
- kinasy AMP aktivovaných proteinkinas MeSH
- krevní glukóza metabolismus MeSH
- krysa rodu Rattus MeSH
- metabolismus lipidů účinky léků MeSH
- metformin krev terapeutické užití MeSH
- modely nemocí na zvířatech MeSH
- myokard metabolismus patologie MeSH
- plíce patologie MeSH
- potkani Wistar MeSH
- preklinické hodnocení léčiv MeSH
- proteinkinasy metabolismus MeSH
- srdeční mitochondrie fyziologie MeSH
- srdeční selhání diagnostické zobrazování farmakoterapie patofyziologie MeSH
- tělesná hmotnost účinky léků MeSH
- ultrasonografie MeSH
- velikost orgánu účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- glykogen MeSH
- hypoglykemika MeSH
- kinasy AMP aktivovaných proteinkinas MeSH
- krevní glukóza MeSH
- metformin MeSH
- proteinkinasy MeSH
Advanced HF (heart failure) is associated with altered substrate metabolism. Whether modification of substrate use improves the course of HF remains unknown. The antihyperglycaemic drug MET (metformin) affects substrate metabolism, and its use might be associated with improved outcome in diabetic HF. The aim of the present study was to examine whether MET would improve cardiac function and survival also in non-diabetic HF. Volume-overload HF was induced in male Wistar rats by creating ACF (aortocaval fistula). Animals were randomized to placebo/MET (300 mg·kg(-1) of body weight·day(-1), 0.5% in food) groups and underwent assessment of metabolism, cardiovascular and mitochondrial functions (n=6-12/group) in advanced HF stage (week 21). A separate cohort served for survival analysis (n=10-90/group). The ACF group had marked cardiac hypertrophy, increased LVEDP (left ventricular end-diastolic pressure) and lung weight confirming decompensated HF, increased circulating NEFAs (non-esterified 'free' fatty acids), intra-abdominal fat depletion, lower glycogen synthesis in the skeletal muscle (diaphragm), lower myocardial triacylglycerol (triglyceride) content and attenuated myocardial (14)C-glucose and (14)C-palmitate oxidation, but preserved mitochondrial respiratory function, glucose tolerance and insulin sensitivity. MET therapy normalized serum NEFAs, decreased myocardial glucose oxidation, increased myocardial palmitate oxidation, but it had no effect on myocardial gene expression, AMPK (AMP-activated protein kinase) signalling, ATP level, mitochondrial respiration, cardiac morphology, function and long-term survival, despite reaching therapeutic serum levels (2.2±0.7 μg/ml). In conclusion, MET-induced enhancement of myocardial fatty acid oxidation had a neutral effect on cardiac function and survival. Recently reported cardioprotective effects of MET may not be universal to all forms of HF and may require AMPK activation or ATP depletion. No increase in mortality on MET supports its safe use in diabetic HF.
Citace poskytuje Crossref.org
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Metabolic characterization of volume overload heart failure due to aorto-caval fistula in rats