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突触后α2-去甲肾上腺素能受体介导室旁核注射去甲肾上腺素和可乐定诱导的进食。

Postsynaptic alpha 2-noradrenergic receptors mediate feeding induced by paraventricular nucleus injection of norepinephrine and clonidine.

作者信息

Goldman C K, Marino L, Leibowitz S F

出版信息

Eur J Pharmacol. 1985 Sep 10;115(1):11-9. doi: 10.1016/0014-2999(85)90578-3.

Abstract

This study examines the feeding response induced by hypothalamic noradrenergic stimulation, in terms of the type and synaptic position of its mediating receptor. Tests with norepinephrine or the alpha 2 receptor agonist clonidine, injected into the area of the paraventricular nucleus (PVN), revealed a potent feeding response in satiated animals. This response by either agonist was blocked, in a dose-dependent fashion, by local injection of the alpha 2-noradrenergic antagonists, rauwolscine and yohimbine. It was also blocked by the general antagonist, phentolamine. In contrast, it was unaffected by hypothalamic injection of the alpha 1-noradrenergic antagonists, prazosin and corynanthine. These results indicate that feeding elicited by noradrenergic stimulation in the region of the PVN is mediated through alpha 2-type receptors. These alpha 2 receptors appear to be located postsynaptically, since the effectiveness of clonidine in eliciting eating was undisturbed by prior injection of the catecholamine synthesis inhibitor, alpha-methyl-p-tyrosine.

摘要

本研究根据介导受体的类型和突触位置,研究下丘脑去甲肾上腺素能刺激所诱发的摄食反应。向室旁核(PVN)区域注射去甲肾上腺素或α2受体激动剂可乐定进行的试验显示,饱足动物会出现强烈的摄食反应。局部注射α2-去甲肾上腺素能拮抗剂萝芙辛和育亨宾,可剂量依赖性地阻断这两种激动剂所引发的这种反应。它也被通用拮抗剂酚妥拉明阻断。相比之下,下丘脑注射α1-去甲肾上腺素能拮抗剂哌唑嗪和育亨宾对其没有影响。这些结果表明,PVN区域去甲肾上腺素能刺激引发摄食是通过α2型受体介导的。这些α2受体似乎位于突触后,因为预先注射儿茶酚胺合成抑制剂α-甲基-p-酪氨酸并不会干扰可乐定引发进食的效果。

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