Regulation of Thirst and Vasopressin Release

被引:40
作者
Bichet, Daniel G. [1 ,2 ]
机构
[1] Univ Montreal, Montreal, PQ H4J 1C5, Canada
[2] Hop Sacre Coeur Montreal, Res Ctr, Serv Nephrol, Montreal, PQ H4J 1C5, Canada
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 81 | 2019年 / 81卷
关键词
thirst; vasopressin; anticipation; lamina terminalis; taste receptors; optogenetics; ADIPSIC HYPERNATREMIA; UNDERLYING THIRST; NEURAL CIRCUITS; SODIUM; TASTE; NEURONS; CONSEQUENCES; APPETITE; SALT; MECHANISMS;
D O I
10.1146/annurev-physiol-020518-114556
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Recent experiments using optogenetic tools facilitate the identification and functional analysis of thirst neurons and vasopressin-producing neurons. Four major advances provide a detailed anatomy and physiology of thirst, taste for water, and arginine-vasopressin (AVP) release: (a) Thirst and AVP release are regulated by the classical homeostatic, interosensory plasma osmolality negative feedback as well as by novel, exterosensory, anticipatory signals. These anticipatory signals for thirst and vasopressin release concentrate on the same homeostatic neurons and circumventricular organs that monitor the composition of blood. (b) Acid-sensing taste receptor cells (TRCs) expressing otopetrin 1 on type III presynaptic TRCs on the tongue, which were previously suggested as the sour taste sensors, also mediate taste responses to water. (c) Dehydration is aversive, and median preoptic nucleus (MnPO) neuron activity is proportional to the intensity of this aversive state. (d) MnPOGLP1R neurons serve as a central detector that discriminates fluid ingestion from solid ingestion, which promotes acute satiation of thirst through the subfornical organ and other downstream targets.
引用
收藏
页码:359 / +
页数:4
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