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机械负荷诱导心房利钠肽分泌的机制:内皮素、一氧化氮和血管紧张素II的作用。

Mechanisms of mechanical load-induced atrial natriuretic peptide secretion: role of endothelin, nitric oxide, and angiotensin II.

作者信息

Ruskoaho H, Leskinen H, Magga J, Taskinen P, Mäntymaa P, Vuolteenaho O, Leppäluoto J

机构信息

Department of Pharmacology and Toxicology, Biocenter Oulu, University of Oulu, Finland.

出版信息

J Mol Med (Berl). 1997 Nov-Dec;75(11-12):876-85. doi: 10.1007/s001090050179.

Abstract

There are three members in the natriuretic peptide hormone family, atrial natriuretic peptide (ANP), B-type natriuretic peptide (BNP, brain natriuretic peptide), and C-type natriuretic peptide (CNP), that are involved in the regulation of blood pressure and fluid homeostasis. CNP is found principally in the central nervous system and vascular endothelial cells while ANP and BNP are cardiac hormones. ANP is synthesized mainly in the atria of the normal adult heart, while BNP is produced by both the atria and ventricles. The mechanisms controlling ANP release have been the subject of intense research, and are now fairly well understood. The major determinant of ANP secretion is myocyte stretch. Although much less is known about the factors regulating BNP release from the heart, myocyte stretch has also been reported to stimulate BNP release from both atria and ventricles. However, whether wall stretch acts directly or via factors such as endothelin- , nitric oxide, or angiotensin II liberated in response to distension has not been established. Recent studies show that by stimulating endothelin type A receptors endothelin plays an important physiological role as a mediator of acute-volume load-induced ANP secretion from atrial myocytes in conscious animals. In fact, endogenous paracrine/autocrine factors liberated in response to atrial wall stretch rather than direct stretch appears to be responsible for activation of ANP secretion in response to volume load, as evidenced by almost complete blockade of ANP secretion during combined inhibition of endothelin type A/B and angiotensin II receptors. Furthermore, under certain experimental conditions angiotensin II and nitric oxide may also exert a significant modulatory effect on stretch-activated ANP secretion. The molecular mechanisms by which endothelin-1, angiotensin II, and nitric oxide synergistically regulate stretch-activated ANP release are yet unclear.

摘要

利钠肽激素家族有三个成员,即心房利钠肽(ANP)、B型利钠肽(BNP,脑利钠肽)和C型利钠肽(CNP),它们参与血压调节和液体平衡。CNP主要存在于中枢神经系统和血管内皮细胞中,而ANP和BNP是心脏激素。ANP主要在正常成年心脏的心房中合成,而BNP由心房和心室产生。控制ANP释放的机制一直是深入研究的课题,目前已相当清楚。ANP分泌的主要决定因素是心肌细胞拉伸。虽然对调节心脏BNP释放的因素了解较少,但也有报道称心肌细胞拉伸可刺激心房和心室释放BNP。然而,壁拉伸是直接起作用还是通过诸如内皮素、一氧化氮或因扩张而释放的血管紧张素II等因素起作用尚未确定。最近的研究表明,在清醒动物中,内皮素通过刺激A型内皮素受体,作为急性容量负荷诱导心房肌细胞分泌ANP的介质发挥重要的生理作用。事实上,对容量负荷的反应中,ANP分泌的激活似乎是由心房壁拉伸释放的内源性旁分泌/自分泌因子而非直接拉伸负责,这一点从同时抑制A型/B型内皮素受体和血管紧张素II受体时ANP分泌几乎完全被阻断可以证明。此外,在某些实验条件下,血管紧张素II和一氧化氮也可能对拉伸激活的ANP分泌产生显著的调节作用。内皮素-1、血管紧张素II和一氧化氮协同调节拉伸激活的ANP释放的分子机制尚不清楚。

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