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钙敏感受体激动剂 OR-1986 对高血压 Dahl/Rapp 大鼠心血管死亡率和心肌重构的影响。

Effects of calcium sensitizer OR-1986 on a cardiovascular mortality and myocardial remodelling in hypertensive Dahl/Rapp rats.

机构信息

Institute of Biomedicine, Pharmacology, University of Helsinki, Finland.

出版信息

J Physiol Pharmacol. 2009 Sep;60(3):41-7.

Abstract

Calcium-sensitizing agents have been shown to improve cardiac function in patients suffering from acute decompensated heart failure, however, their long-term effects on cardiac remodeling and cardiovascular mortality are still largely unknown. In the present study we tested the hypothesis whether OR-1896, an active and long-lasting metabolite of calcium sensitizer levosimendan, prevents cardiovascular mortality and hypertension-induced myocardial remodelling in salt-sensitive Dahl/Rapp rats. OR-1896 was given orally to Dahl/Rapp SS rats on high-salt diet (NaCl 7% w/w) for 7 weeks at two different doses (0.5 and 0.05 mg/kg). OR-1896 prevented salt-induced cardiovascular mortality (survival rate 75 % in OR-1896 treated groups vs 38 % in untreated controls, p<0.01), ameliorated cardiac hypertrophy and improved systolic functions of the heart without major influence on systemic blood pressure. OR-1896 also ameliorated salt-induced increase in cardiac ANP mRNA expression and plasma BNP level. Salt-induced cardiac remodelling was associated with 4-fold increase in cardiac p16(INK4a) mRNA expression, a marker of cellular senescence. OR-1896 dose-dependently ameliorated cardiomyocyte senescence. Our findings suggest a therapeutic role for OR-1896 in the prevention of cardiac remodelling in salt-sensitive forms of hypertension. The present study also underscores the importance of cellular senescence in the pathogenesis of salt-induced hypertensive heart disease.

摘要

钙敏化剂已被证明可改善急性失代偿性心力衰竭患者的心脏功能,但它们对心脏重构和心血管死亡率的长期影响仍知之甚少。在本研究中,我们检验了假设,即钙敏剂左西孟旦的活性和长效代谢物 OR-1896 是否可预防盐敏感型 Dahl/Rapp 大鼠中的心血管死亡率和高血压引起的心肌重构。在高盐饮食(NaCl 7%w/w)下,OR-1896 以 2 种不同剂量(0.5 和 0.05 mg/kg)经口给予 Dahl/Rapp SS 大鼠 7 周。OR-1896 可预防盐诱导的心血管死亡率(OR-1896 治疗组的存活率为 75%,未治疗对照组为 38%,p<0.01),改善心脏肥大并改善心脏的收缩功能,而对全身血压无重大影响。OR-1896 还可改善盐诱导的心脏 ANP mRNA 表达和血浆 BNP 水平的增加。盐诱导的心脏重构与心脏 p16(INK4a)mRNA 表达增加 4 倍有关,p16(INK4a)mRNA 表达是细胞衰老的标志物。OR-1896 呈剂量依赖性改善心肌细胞衰老。我们的研究结果表明,OR-1896 在预防盐敏感性高血压形式的心脏重构方面具有治疗作用。本研究还强调了细胞衰老在盐诱导的高血压性心脏病发病机制中的重要性。

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