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多种神经活性物质对脑片下丘脑弓状核神经元单单位活动的影响。

Effects of various neuroactive substances on single-unit activities of hypothalamic arcuate neurons in brain slices.

作者信息

Lin J Y, Li C S, Pan J T

机构信息

Institute of Physiology, National Yang-Ming Medical College, Taipei, Taiwan, Republic of China.

出版信息

Brain Res Bull. 1993;31(5):587-94. doi: 10.1016/0361-9230(93)90127-w.

Abstract

Extracellular single-unit activities of 288 dorsomedial/ventrolateral hypothalamic arcuate (ARC) neurons were studied electrophysiologically in brain slices in vitro. We tested the effects of several neuroactive substances plus some of their analogs in this study. Among them, baclofen, a GABAb-receptor agonist, inhibited 95.6% of ARC neurons tested, although GABA itself was much less effective (23.8%). About half of baclofen's effect was blocked by phaclofen, a GABAB antagonist. Serotonin and dopamine also exhibited mostly inhibitory effects on responsive ARC neurons (80 and 78.4%, respectively), although more than half ARC neurons tested (53.3% of 169) were not responsive to dopamine. Neither ketanserin, a 5-HT2, nor domperidone, a D2 receptor antagonist, had much effect on blocking the actions of 5-HT or DA. Histamine and carbachol excited 67.4% and 52.2% of ARC neurons tested, respectively. Moreover, their effects were completely blocked by pyrilamine, a H1, and atropine, a muscarinic receptor antagonist, respectively. Ranitidine, a H2 receptor antagonist, however, was less effective. Norepinephrine had about equal number of excitation (33.3%) and inhibition (38.5%) on ARC neurons. Cholecystokinin-octapeptide sulphate (CCK-8S), a neuropeptide tested exerted potent excitatory effects on ARC neurons (62.8% of 137). In summary, ARC neurons in a more localized region aiming at the tuberoinfundibular dopaminergic neurons were selected in this study. Their responses to many agents and the implications on the regulation of prolactin secretion were discussed.

摘要

在体外脑片中,通过电生理学方法研究了288个下丘脑背内侧/腹外侧弓状核(ARC)神经元的细胞外单单位活动。在本研究中,我们测试了几种神经活性物质及其一些类似物的作用。其中,GABAb受体激动剂巴氯芬抑制了95.6%的受试ARC神经元,而GABA本身的效果则差得多(23.8%)。巴氯芬约一半的作用被GABAB拮抗剂法氯芬阻断。血清素和多巴胺对反应性ARC神经元也大多表现出抑制作用(分别为80%和78.4%),尽管超过一半的受试ARC神经元(169个中的53.3%)对多巴胺无反应。5-HT2拮抗剂酮色林和D2受体拮抗剂多潘立酮对阻断5-HT或DA的作用均无太大影响。组胺和卡巴胆碱分别兴奋了67.4%和52.2%的受试ARC神经元。此外,它们的作用分别被H1拮抗剂吡苄明和毒蕈碱受体拮抗剂阿托品完全阻断。然而,H2受体拮抗剂雷尼替丁的效果较差。去甲肾上腺素对ARC神经元的兴奋作用(33.3%)和抑制作用(38.5%)数量大致相等。所测试的神经肽硫酸胆囊收缩素八肽(CCK-8S)对ARC神经元有强大的兴奋作用(137个中的62.8%)。总之,本研究选择了一个更局限区域内针对结节漏斗多巴胺能神经元的ARC神经元。讨论了它们对多种药物的反应以及对催乳素分泌调节的意义。

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