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[用于治疗血流动力学紊乱的血管加压素]

[Vasopressin for treatment of hemodynamic disorders].

作者信息

Adukauskiene Dalia, Sirvinskas Edmundas, Kevelaitis Egidijus

机构信息

Clinic of Intensive Therapy, Kaunas University of Medicine, Eiveniu 2, 50009 Kaunas, Lithuania.

出版信息

Medicina (Kaunas). 2008;44(2):167-73.

Abstract

Vasopressin is a 9-amino acid peptide synthesized by magnocellular neurons of the hypothalamus and released from posterior pituitary gland. The primary physiological role of vasopressin is the maintenance of fluid homeostasis. In this review, the classification of vasopressin receptors, namely V1 vascular, V2 renal, V3 pituitary, oxytocin receptors, and purinergic receptors, and the effects of vasopressin on vascular smooth muscles, the heart, and the kidneys are discussed. Mortality rates of vasodilatory (or distributive), for example septic shock, are high. The use of vasopressin is an alternative therapy for vasodilatory shock with better outcome. Vasopressin is effective in resuscitation of adults after ventricular fibrillation or pulseless tachycardia, when epinephrine is not effective.

摘要

血管加压素是一种由下丘脑大细胞神经元合成并从垂体后叶释放的九氨基酸肽。血管加压素的主要生理作用是维持液体平衡。在本综述中,讨论了血管加压素受体的分类,即V1血管受体、V2肾受体、V3垂体受体、催产素受体和嘌呤能受体,以及血管加压素对血管平滑肌、心脏和肾脏的影响。例如感染性休克等血管扩张性(或分布性)休克的死亡率很高。使用血管加压素是治疗血管扩张性休克的一种替代疗法,效果更好。当肾上腺素无效时,血管加压素对心室颤动或无脉性心动过速后的成人复苏有效。

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