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心脏对利钠肽分泌的调节。

Regulation of natriuretic peptide secretion by the heart.

作者信息

Thibault G, Amiri F, Garcia R

机构信息

Laboratory of Cell Biology of Hypertension, Clinical Research Institute of Montreal, Quebec, Canada.

出版信息

Annu Rev Physiol. 1999;61:193-217. doi: 10.1146/annurev.physiol.61.1.193.

Abstract

Secreted by the heart, more specifically by atrial cardiomyocytes under normal conditions but also by ventricular myocytes during cardiac hypertrophy, natriuretic peptides are now considered important hormones in the control of blood pressure and salt and water excretion. Studies on natriuretic peptide secretagogues and their mechanisms of action have been complicated by hemodynamic changes and contractions to which the atria are constantly subjected. It now appears that atrial stretch through mechano-sensitive ion channels, adrenergic stimulation via alpha 1A-adrenergic receptors, and endothelin via its ETA receptor subtype are major triggering agents of natriuretic peptide release. With several other stimuli, such as angiotensin II and beta-adrenergic agents, modulation of natriuretic peptide release appears to be linked to local generation of prostaglandins. In all cases, intracellular calcium homeostasis, controlled by several ion channels, is considered a key element in the regulation of natriuretic peptide secretion.

摘要

利钠肽由心脏分泌,在正常情况下更具体地由心房心肌细胞分泌,但在心脏肥大时心室肌细胞也会分泌。目前,利钠肽被认为是控制血压以及盐和水排泄的重要激素。利钠肽促分泌剂及其作用机制的研究因心房不断受到的血流动力学变化和收缩而变得复杂。现在看来,通过机械敏感离子通道的心房牵张、经由α1A-肾上腺素能受体的肾上腺素能刺激以及通过其ETA受体亚型的内皮素是利钠肽释放的主要触发因素。对于其他几种刺激,如血管紧张素II和β-肾上腺素能药物,利钠肽释放的调节似乎与前列腺素的局部生成有关。在所有情况下,由几种离子通道控制的细胞内钙稳态被认为是利钠肽分泌调节的关键因素。

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