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心房利钠多肽释放的生化机制。

Biochemical mechanism of release of atrial natriuretic polypeptide.

作者信息

Hayashi J, Ohni M, Manabe H, Watanabe Y

机构信息

Cardiovascular Institute, Fujita Gakuen Health University, Aichi, Japan.

出版信息

Jpn Circ J. 1988 Dec;52(12):1421-4. doi: 10.1253/jcj.52.1421.

Abstract

To define transmembrane and intracellular mechanisms of production and release of atrial natriuretic polypeptide (ANP) in the absence of mechanical atrial stretch, we studied the direct effects of physiological stimuli on isolated adult rat atrial myocytes maintained under tissue culture. Although stimulation of beta-adrenergic receptors on the surface of atrial myocytes by isoproterenol did not affect ANP release, adrenergic alpha-1 receptor stimulation by methoxamine enhanced ANP release with reciprocal intracellular ANP reduction. When muscarinic receptors were stimulated by acetylcholine, ANP release was accelerated and intracellular ANP reduced. The activation of the phosphatidylinositol system, which is a common pathway for muscarinic and alpha-1 adrenergic receptor stimulation, was thus considered to regulate ANP release, but not ANP production.

摘要

为了确定在心房无机械牵张情况下心房利钠多肽(ANP)产生和释放的跨膜及细胞内机制,我们研究了生理刺激对组织培养条件下成年大鼠离体心房肌细胞的直接影响。尽管异丙肾上腺素对心房肌细胞表面β - 肾上腺素能受体的刺激不影响ANP释放,但甲氧明对肾上腺素能α - 1受体的刺激可增强ANP释放,同时细胞内ANP相应减少。当乙酰胆碱刺激毒蕈碱受体时,ANP释放加速,细胞内ANP减少。因此,磷脂酰肌醇系统的激活被认为是调节ANP释放而非ANP产生的机制,磷脂酰肌醇系统是毒蕈碱和α - 1肾上腺素能受体刺激的共同途径。

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