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垂体腺苷酸环化酶激活多肽作为一种心脏保护因子对培养的大鼠心肌细胞的作用。

The effect of pituitary adenylate cyclase activating polypeptide on cultured rat cardiocytes as a cardioprotective factor.

作者信息

Sano Hirofumi, Miyata Atsuro, Horio Takeshi, Nishikimi Toshio, Matsuo Hisayuki, Kangawa Kenji

机构信息

National Cardiovascular Center Research Institute, Suita, Osaka, Japan.

出版信息

Regul Pept. 2002 Nov 15;109(1-3):107-13. doi: 10.1016/s0167-0115(02)00193-3.

Abstract

In the cardiovascular system, pituitary adenylate cyclase activating polypeptide (PACAP) exhibits not only vasodilation but also positive inotropic action by increasing cardiac output. Then the effect of PACAP in cultured cardiovascular cells was examined. In neonatal rat myocytes, PACAP evoked concentration-dependent increase in intracellular cyclic AMP content more potently than vasoactive intestinal polypeptide (VIP). However, in neonatal rat nonmyocytes, PACAP and VIP showed equal potency. The characterization of the subtype of PACAP/VIP receptors by RT-PCR analysis revealed that PAC1 receptor mRNA is dominantly present in the myocytes, but VPAC2 receptor mRNA is abundant in the nonmyocytes. In the myocytes, PACAP did not change the protein synthesis stimulated by endothelin or by itself. However, PACAP moderately stimulated the secretion of atrial natriuretic polypeptide (ANP). On the other hand, PACAP inhibited the protein synthesis and DNA synthesis of the nonmyocytes. These indicate that PACAP might be involved in the regulation of cardiac hypertrophy and fibrosis as a cardioprotective factor.

摘要

在心血管系统中,垂体腺苷酸环化酶激活多肽(PACAP)不仅具有血管舒张作用,还可通过增加心输出量发挥正性肌力作用。随后研究了PACAP对培养的心血管细胞的影响。在新生大鼠心肌细胞中,PACAP比血管活性肠肽(VIP)更有效地引起细胞内环磷酸腺苷(cAMP)含量的浓度依赖性增加。然而,在新生大鼠非心肌细胞中,PACAP和VIP的效力相当。通过逆转录聚合酶链反应(RT-PCR)分析对PACAP/VIP受体亚型进行表征,结果显示PAC1受体mRNA主要存在于心肌细胞中,而VPAC2受体mRNA在非心肌细胞中大量存在。在心肌细胞中,PACAP不会改变由内皮素或其自身刺激引起的蛋白质合成。然而,PACAP适度刺激心房利钠多肽(ANP)的分泌。另一方面,PACAP抑制非心肌细胞的蛋白质合成和DNA合成。这些表明PACAP可能作为一种心脏保护因子参与心脏肥大和纤维化的调节。

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