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血管加压素:生理学、评估和渗透压感知。

Vasopressin: physiology, assessment and osmosensation.

机构信息

Centre de Recherche des Cordeliers, INSERM Unit 1138, 75006, Paris, France.

Université Pierre et Marie Curie, 75006, Paris, France.

出版信息

J Intern Med. 2017 Oct;282(4):284-297. doi: 10.1111/joim.12645. Epub 2017 Jul 26.

DOI:10.1111/joim.12645
PMID:28649750
Abstract

Vasopressin (AVP) plays a major role in the regulation of water and sodium homeostasis by its antidiuretic action on the kidney, mediated by V2 receptors. AVP secretion is stimulated by a rise in plasma osmolality, a decline in blood volume or stress. V1a receptors are expressed in vascular smooth muscle cells, but the role of vasopressin in blood pressure regulation is still a matter of debate. AVP may also play a role in some metabolic pathways, including gluconeogenesis, through its action on V1a receptors expressed in the liver. It is now understood that thirst and arginine vasopressin (AVP) release are regulated not only by the classical homeostatic, intero-sensory plasma osmolality negative feedback, but also by novel, extero-sensory, anticipatory signals. AVP measurement is time-consuming, and AVP level in the blood in the physiological range is often below the detection limit of the assays. Recently, an immunoassay has been developed for the measurement of copeptin, a fragment of the pre-provasopressin molecule that is easier to measure. It has been shown to be a good surrogate marker of AVP.

摘要

血管加压素(AVP)通过肾脏的 V2 受体发挥抗利尿作用,在水和钠稳态的调节中起主要作用。AVP 的分泌受血浆渗透压升高、血容量下降或应激刺激。V1a 受体在血管平滑肌细胞中表达,但血管加压素在血压调节中的作用仍存在争议。AVP 还可能通过其在肝脏中表达的 V1a 受体在某些代谢途径中发挥作用,包括糖异生。现在人们已经了解到,口渴和精氨酸血管加压素(AVP)的释放不仅受到经典的、内感受性血浆渗透压负反馈的调节,还受到新的、外感受性、预期性信号的调节。AVP 的测量很耗时,而且血液中生理范围内的 AVP 水平通常低于检测方法的检测限。最近,开发了一种用于测量 copeptin 的免疫测定法,copeptin 是前血管加压素分子的片段,更容易测量。已经证明它是 AVP 的良好替代标志物。

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