The role of endothelin-converting enzyme-1 in the development of alpha(1)-adrenergic-stimulated hypertrophy in cultured neonatal rat cardiac myocytes

Article

关键词: GENE-EXPRESSION;    HEART-FAILURE;    VENTRICULAR HYPERTROPHY;    RECEPTOR ANTAGONIST;    CARDIOMYOPATHY;    INDUCTION;    MECHANISM;    PATHWAY;    CLONING;    KINASE;   

DOI  :  10.1161/01.CIR.99.2.292

来源: SCIE

【 摘 要 】

Background-Accumulating evidence suggests that the local synthesis of endotheIin-1 (ET-1) plays a role in the development of heart failure in vivo. We investigated the role of endothelin-converting enzyme-1 (ECE-1), which mediates the conversion of big ET-1 to mature ET-1, in the development of alpha(1)-adrenergic-stimulated hypertrophy in cultured neonatal rat cardiac myocytes. Methods and Results-Phenylephrine (PE) induced the expression of ET-1 in rat cardiac myocytes and accelerated the conversion of big ET-1 to ET-1. The ECE-1 mRNA levels were markedly increased 3 hours after PE stimulation (3.6-fold compared with saline stimulation, P<0.005). A specific ECE-1 antagonist, FR901533, inhibited the PE-stimulated increase in protein synthesis rate by 45% (P<0.05). As genetic markers for the hypertrophic response, FR901533 inhibited the PE-stimulated transcriptional activities of the 3.5-kb beta-myosin heavy chain promoter by 79% (P<0.01) but did not affect that of- the 3.4-kb atrial natriuretic factor (ANF) promoter. In Bio14.6 Syrian cardiomyopathic hamsters, ventricular ET-1 and ANF mRNA levels did not correlate at 2 different stages. Conclusions-ET-1-independent pathways may mediate activation of the ANF gene program in ventricular myocytes both in vitro and in vivo. These results also indicate that the conversion of big ET-1 to ET-1 in rat cardiac myocytes is required for the development of alpha(1)-adrenergic-stimulated hypertrophy and beta-myosin heavy chain gene transcription.

【 授权许可】

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