Ghrelin improves disturbed myocardial energy metabolism in rats with heart failure induced by isoproterenol

被引:15
作者
Xu, Jian-Ping [1 ]
Wang, Hong-Xia [1 ]
Wang, Wen [1 ]
Zhang, Li-Ke [1 ]
Tang, Chao-Shu [1 ,2 ]
机构
[1] Capital Med Univ, Dept Physiol & Pathophysiol, Beijing 100069, Peoples R China
[2] Peking Univ, Inst Cardiovasc Res, Hosp 1, Beijing 100034, Peoples R China
基金
中国国家自然科学基金;
关键词
ghrelin; metabolism; heart failure; glucose; lactate; monocarboxylate transporter-1; GHS-R; DES-OCTANOYL GHRELIN; CARBOHYDRATE-METABOLISM; GUT HORMONES; CACHEXIA; PREVENTS; RECEPTOR; PEPTIDE; INJURY; MODEL; MASS;
D O I
10.1002/psc.1253
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To explore the effects of ghrelin on disturbed myocardial energy metabolism during chronic heart failure (CHF). Rats were subcutaneously injected with isoproterenol (ISO) for 10 days with or without ghrelin for another 10 days. Enzyme immunoassay was to measure ghrelin concentrations. Compared with the control group, ISO-treated rats showed suppressed cardiac function with high ghrelin/GHS-R expressions. These rats also showed the decreases in food consumption and weight. The decreased levels of plasma glucose and myocardial glucogen, but the high lactate in blood and myocardium showed myocardial metabolic disturbance. Compared with the group given ISO alone, the rats with ghrelin (20 and 100 mu g/kg/day) improved cardiac dysfunction and increased food intake by 13.5 and 14.2% (both P < 0.01), and rate of weight gain by 95% (P < 0.05) and 1.71-fold (P < 0.01), respectively. The plasma glucose were increased by 49.7 and 50.8% (both P < 0.01), and myocardial glucogen, by 40.5 and 51.7% (both P < 0.01), but blood lactate decreased by 1.56- and 1.96-fold (both P < 0.01), and myocardial lactate by 32.1 and 48.7% (both P < 0.05), respectively. Their MCT1 mRNA and protein expressions increased. The myocardial ghrelin/GHS-R pathway can be upregulated during CHF. The ghrelin can attenuate cardiac dysfunction and energy metabolic disturbance in CHF rats. Copyright (C) 2010 European Peptide Society and John Wiley & Sons, Ltd.
引用
收藏
页码:392 / 402
页数:11
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