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Regulation of Thirst and Vasopressin Release

机译:调节口渴和血管加压素释放

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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.
机译:最近使用致光学工具的实验促进了渴望神经元和血压加强素的神经元的鉴定和功能分析。四个主要进展提供了渴望,水味的详细解剖和生理学,以及精氨酸 - 血管加压素(AVP)释放:(a)渴望和AVP释放由经典的稳态,中间血浆渗透性负反馈以及新颖,外部传递,预期信号。这些预期的胃泌素和血管加压素释放的信号浓缩在同一个稳压神经元和周上器官上,监测血液组成。 (b)酸感测味道受体细胞(TRC)在舌型上表达III型突触前TRC的耳虫1,其先前提出作为酸性味道传感器,也介绍了对水的味道反应。 (c)脱水是厌恶的,中位数核(MNPO)神经元活性与该厌恶状态的强度成比例。 (d)MNPoGLP1R神经元用作中央检测器,其区分从固体摄入的液体摄取,这促进了通过子学器官和其他下游靶标的急性饱满。

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