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大鼠脑隔区的V1-血管加压素受体。电生理学证据。

V1-vasopressin receptors in the septum of the rat brain. Electrophysiological evidence.

作者信息

Raggenbass M, Tribollet E, Dreifuss J J

机构信息

Department of Physiology, University Medical Center, Geneva, Switzerland.

出版信息

J Recept Res. 1988;8(1-4):261-71. doi: 10.3109/10799898809048991.

Abstract

In slices from the rat brain, extracellular recordings were obtained from single neurones located in the lateral septum, an area known to receive a vasopressinergic innervation. Approximately half of the neurones tested responded to vasopressin by a concentration-dependent increase in firing rate, the lowest effective concentration being in the order of 2 nM. The effect of vasopressin was blocked by a synthetic structural analogue possessing vasopressor and oxytocic antagonistic properties on peripheral vasopressin and oxytocin receptors. Oxytocin had a weak effect in firing septal neurones, whereas a selective oxytocic agonist was totally ineffective. The action of vasopressin on neuronal firing was mimicked by a vasopressor agonist (Phe2-Orn8-VT) but not by a selective antidiuretic agonist (dDAVP). These results indicate that the vasopressin receptors present in rat septum are V1 (vasopressor type) rather than V2 (antidiuretic type) receptors. In addition, we conclude that these receptors, when occupied, lead to increased firing of lateral septal neurones.

摘要

在大鼠脑切片中,从位于外侧隔区的单个神经元进行细胞外记录,该区域已知接受血管加压素能神经支配。大约一半接受测试的神经元对血管加压素产生反应,放电频率呈浓度依赖性增加,最低有效浓度约为2 nM。血管加压素的作用被一种对周围血管加压素和催产素受体具有血管升压和催产拮抗特性的合成结构类似物所阻断。催产素对隔区神经元放电的影响较弱,而一种选择性催产素激动剂则完全无效。血管升压激动剂(Phe2-Orn8-VT)可模拟血管加压素对神经元放电的作用,但选择性抗利尿激动剂(dDAVP)则不能。这些结果表明,大鼠隔区存在的血管加压素受体是V1(血管升压型)而非V2(抗利尿型)受体。此外,我们得出结论,这些受体被占据时会导致外侧隔区神经元放电增加。

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