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首页> 外文期刊>Brain research bulletin >Roles of forebrain GABA receptors in controlling vasopressin secretion and related phenomena under basal and hyperosmotic circumstances in conscious rats.
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Roles of forebrain GABA receptors in controlling vasopressin secretion and related phenomena under basal and hyperosmotic circumstances in conscious rats.

机译:基础和高渗环境下前脑大鼠前脑GABA受体在控制血管加压素分泌及相关现象中的作用。

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摘要

Although the anteroventral third ventricular region (AV3V), a forebrain area essential for homeostatic responses, includes receptors for gamma-aminobutyric acid (GABA), the roles of these receptors in controlling vasopressin (AVP) secretion and related phenomena have not been clarified as yet. This study aimed to pursue this problem in conscious rats implanted with indwelling catheters. Cerebral injection sites were determined histologically. Applications of bicuculline, a GABA(A) receptor antagonist, to the AV3V induced prompt and marked augmentations in plasma AVP, osmolality, glucose, arterial pressure and heart rate, without affecting plasma electrolytes. Such phenomena did not occur when phaclofen, a GABA(B) receptor antagonist, was applied to the AV3V. All of the effects of AV3V-administered bicuculline were abolished by preadministration of the GABA(A) receptor agonist muscimol. Preadministration of either MK-801 or NBQX, ionotropic glutamatergic receptor antagonists, was also potent to abolish the AVP response to AV3V bicuculline. When hypertonic saline was infused intravenously, plasma AVP increased progressively, in parallel with rises in plasma osmolality, sodium and arterial pressure. AV3V application of muscimol or baclofen, a GABA(B) receptor agonist, was found to abolish the response of plasma AVP, without inhibiting that of the osmolality or sodium. The response of arterial pressure was also blocked by muscimol treatment, but not by baclofen treatment. Based on these results, we concluded that, under basal conditions, GABA receptors in the AV3V or vicinity may tonically operate to attenuate AVP secretion and cardiovascular functions through mechanisms associated with glutamatergic activity, and that plasma hyperosmolality may cause facilitation of AVP release by decreasing forebrain GABAergic activity.
机译:尽管前脑第三脑室区域(AV3V)是稳态反应必不可少的前脑区域,其中包含γ-氨基丁酸(GABA)受体,但这些受体在控制血管加压素(AVP)分泌和相关现象中的作用尚未阐明。这项研究的目的是在植入留置导管的清醒大鼠中解决这个问题。通过组织学确定脑注射部位。 Gcu(GABA(A)受体拮抗剂)双小分子在AV3V上的应用可引起血浆AVP,重量克分子渗透压浓度,葡萄糖,动脉压和心率的迅速而显着增加,而不会影响血浆电解质。当将GABA(B)受体拮抗剂cloclofen应用于AV3V时,不会发生这种现象。预先施用GABA(A)受体激动剂麝香酚可以消除AV3V施用的双小分子的所有作用。预先施用离子型谷氨酸能受体拮抗剂MK-801或NBQX也可以消除对AV3V双小分子的AVP反应。静脉输注高渗盐水时,血浆AVP逐渐增加,同时血浆渗透压,钠和动脉压升高。发现对muscimol或巴氯芬(一种GABA(B)受体激动剂)进行AV3V施用可消除血浆AVP的反应,而不会抑制同渗容摩尔浓度或钠的浓度。麝香酚治疗也可阻断动脉压的反应,但巴氯芬治疗则不会。根据这些结果,我们得出结论,在基础条件下,AV3V或附近的GABA受体可能通过与谷氨酸能活动相关的机制来调节音频,从而减弱AVP的分泌和心血管功能,血浆高渗性可能通过减少前脑来促进AVP的释放。 GABA能活动。

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