Triple nutrient supplementation improves survival, infarct size and cardiac function following myocardial infarction in rats

被引:9
作者
Briet, Francoise [1 ,4 ,5 ]
Keith, Mary [2 ,4 ,5 ]
Leong-Poi, Howard [3 ,4 ,5 ]
Kadakia, Ankit [1 ,2 ]
Aba-Alkhail, Khalid [2 ]
Giliberto, John-Paul [2 ]
Stewart, Duncan [3 ,4 ,5 ,6 ]
Errett, Lee [2 ,4 ,5 ]
Mazer, C. David [1 ,4 ,5 ,6 ]
机构
[1] St Michaels Hosp, Dept Anesthesia, Toronto, ON M5B 1W8, Canada
[2] St Michaels Hosp, Div Cardiovasc Surg, Toronto, ON M5B 1W8, Canada
[3] St Michaels Hosp, Div Cardiol, Toronto, ON M5B 1W8, Canada
[4] St Michaels Hosp, Terrence Donnelly Heart Ctr, Toronto, ON M5B 1W8, Canada
[5] St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
[6] Univ Toronto, Dept Physiol, Toronto, ON, Canada
关键词
Carnitine; Coenzyme Q(10); Taurine; Cardioprotection; Myocardial infarction;
D O I
10.1016/j.numecd.2007.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aim: We evaluated the impact of triple nutrient supplementation (TNS: carnitine, taurine and coenzyme Q(10)) vs. carnitine atone (CARN) or placebo on survival, infarct size, cardiac function and metabolic gene expression using a model of myocardial infarction (MI) in rats. Methods and results: Male Wistar rats were randomized to three groups divided in two independent studies prior to ligation of the left anterior descending coronary artery (LAD): TNS vs. Placebo and TNS vs. CARN. Nutrient supplementation [L-carnitine (300 mg/day), coenzyme Q(10) (15 mg/kg body weight/day) and taurine (0.1 M)] was administered daily for four weeks prior to and for 10 days after MI. At that time, cardiac function and infarct size were measured. Metabolic gene (mRNA) expression in the peri-infarct tissue of left ventricle from TNS, placebo or corresponding time-control rats (TNS or placebo without LAD ligation) was measured 10 days after MI. When compared to placebo, TNS significantly improved survival (60% vs. 34%, p < 0.02), cardiac function, and reduced infarct size (30 +/- 7% vs. 42 +/- 9%, p < 0.001). Although CARN improved survival like TNS (45% vs. 50%, not significant), it did not reduce infarct size (32 +/- 14% vs. 19 +/- 10%, p < 0.05) or delay myocardial remodeling. In the placebo group, MI was associated with a significantly altered pattern of metabolic gene expression (glucose transporter 1, liver carnitine palmitoyl transferase 1, medium-chain acyl-CoA dehydrogenase; p < 0.01 for all three) in the left ventricle peri-infarct tissue. In contrast, gene expression was normalized in the group receiving TNS. Conclusions: Our results support the potential cardioprotective impact of TNS during myocardial ischemia. In contrast to carnitine supplementation atone, TNS improved survival as well as cardiac function, gene expression and delayed remodeling. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:691 / 699
页数:9
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