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体内,α-和β-肾上腺素能机制相互拮抗,介导去甲肾上腺素对视上核血管加压素神经元的剂量依赖性作用。

Opposing alpha- and beta-adrenergic mechanisms mediate dose-dependent actions of noradrenaline on supraoptic vasopressin neurones in vivo.

作者信息

Day T A, Randle J C, Renaud L P

出版信息

Brain Res. 1985 Dec 9;358(1-2):171-9. doi: 10.1016/0006-8993(85)90961-8.

Abstract

The effects of pressure-applied noradrenaline (NA) on the activity of neurosecretory cells of the supraoptic nucleus (SON) were examined in anaesthetized male rats. Spontaneously active, antidromically identified neurosecretory cells were classified as vasopressin (VP)-secreting on the basis of activity patterns and responsiveness to baroreceptor activation. The probability of encountering VP units was enhanced by confining electrode penetrations to the caudal aspect of the SON. Application of low concentrations of NA (50-150 microM) excited 75% of putative VP neurones tested (n = 45), while very high concentrations (1-100 mM) were inhibitory (79%, n tested = 14). The excitatory effects of NA were blocked by the alpha 1 antagonist prazosin (0.1-5 microM, n = 9) and mimicked by application of the alpha 1 agonist methoxamine (300 microM-1 mM, n = 29). The alpha 2 agonist clonidine (800 microM-1 mM) also frequently elicited mild excitations (92%, n tested = 13); however, this was commonly followed by an extended period of quiescence. Neither the alpha 2 antagonist yohimbine (5 microM, n = 4) nor the beta-adrenoreceptor antagonist timolol (5-20 microM, n = 6) blocked NA-induced excitations. The inhibitory effects of high concentrations of NA, however, were blocked by the application of timolol (5-20 microM, n = 5). It is suggested that the excitatory effect of low concentrations of NA on VP neurones reflects the actions of this substance when endogenously secreted at normal sites of release within the SON.

摘要

在麻醉的雄性大鼠中研究了加压去甲肾上腺素(NA)对视上核(SON)神经分泌细胞活性的影响。根据活动模式和对压力感受器激活的反应性,将自发活动、经逆向鉴定的神经分泌细胞分类为分泌血管加压素(VP)的细胞。将电极穿刺限制在SON的尾侧部分可提高遇到VP单位的概率。低浓度NA(50-150微摩尔)可使75%的受试假定VP神经元兴奋(n = 45),而非常高的浓度(1-100毫摩尔)则具有抑制作用(79%,n受试 = 14)。NA的兴奋作用被α1拮抗剂哌唑嗪(0.1-5微摩尔,n = 9)阻断,并被α1激动剂甲氧明(300微摩尔-1毫摩尔,n = 29)模拟。α2激动剂可乐定(800微摩尔-1毫摩尔)也经常引起轻度兴奋(92%,n受试 = 13);然而,这通常随后会有一段较长的静止期。α2拮抗剂育亨宾(5微摩尔,n = 4)和β肾上腺素能受体拮抗剂噻吗洛尔(5-20微摩尔,n = 6)均未阻断NA诱导的兴奋。然而,高浓度NA的抑制作用可被噻吗洛尔(5-20微摩尔,n = 5)阻断。提示低浓度NA对VP神经元的兴奋作用反映了该物质在SON内正常释放部位内源性分泌时的作用。

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