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Trimetazidine does not alter metabolic substrate oxidation in cardiac mitochondria of target patient population


Ćavar, Marija; Ljubković, Marko; Bulat, Cristijan; Baković, Darija; Fabijanić, Damir; Kraljević, Jasenka; Karanović, Nenad; Dujić, Željko; Lavie, Carl J.; Wisløff, Ulrik; Marinović, Jasna.
Trimetazidine does not alter metabolic substrate oxidation in cardiac mitochondria of target patient population // British journal of pharmacology, 173 (2016), 9; 1529-1540 doi:10.1111/bph.13454 (međunarodna recenzija, članak, znanstveni)


Naslov
Trimetazidine does not alter metabolic substrate oxidation in cardiac mitochondria of target patient population

Autori
Ćavar, Marija ; Ljubković, Marko ; Bulat, Cristijan ; Baković, Darija ; Fabijanić, Damir ; Kraljević, Jasenka ; Karanović, Nenad ; Dujić, Željko ; Lavie, Carl J. ; Wisløff, Ulrik ; Marinović, Jasna.

Izvornik
British journal of pharmacology (0007-1188) 173 (2016), 9; 1529-1540

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Coronary artery disease; trimetazidine; cardiac metabolism; mitochondria; B-oxidation

Sažetak
Trimetazidine, known as a metabolic modulator, is an anti-anginal drug used for treatment of stable coronary artery disease (CAD). It is proposed to act via modulation of cardiac metabolism, shifting the mitochondrial substrate utilization towards carbohydrates, thus increasing the efficiency of ATP production. This mechanism was recently challenged ; however, these studies used indirect approaches and animal models, which made their conclusions questionable. The goal of the current study was to assess the effect of trimetazidine on mitochondrial substrate oxidation directly in left ventricular myocardium from CAD patients. EXPERIMENTAL APPROACH: Mitochondrial fatty acid (palmitoylcarnitine) and carbohydrate (pyruvate) oxidation were measured in permeabilized left ventricular fibres obtained during coronary artery bypass grafting surgery from CAD patients, which either had trimetazidine included in their therapy (TMZ group) or not (Control). KEY RESULTS: There was no difference between the two groups in the oxidation of either palmitoylcarnitine or pyruvate, and in the ratio of carbohydrate to fatty acid oxidation. Activity and expression of pyruvate dehydrogenase, the key regulator of carbohydrate metabolism, were also not different. Lastly, acute in vitro exposure of myocardial tissue to different concentrations of trimetazidine did not affect myocardial oxidation of fatty acid. CONCLUSION AND IMPLICATIONS: Using myocardial tissue from CAD patients, we found that trimetazidine (applied chronically in vivo or acutely in vitro) had no effect on cardiac fatty acid and carbohydrate oxidation, suggesting that the clinical effects of trimetazidine are unlikely to be due to its metabolic effects, but rather to an as yet unidentified intracardiac mechanism.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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