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抗抑郁药物可增强海马切片中的α1-肾上腺素能受体效应。

Antidepressant drugs potentiate the alpha 1-adrenoceptor effect in hippocampal slices.

作者信息

Bijak M

机构信息

Polish Academy of Sciences, Institute of Pharmacology, Krakow.

出版信息

Eur J Pharmacol. 1989 Jul 18;166(2):183-91. doi: 10.1016/0014-2999(89)90058-7.

Abstract

The effect of prolonged treatment with antidepressant drugs on the phenylephrine- and norepinephrine (NE)-evoked reaction in hippocampal slices was examined by extracellular recording of the spontaneous activity of CA1 layer neurons. The alpha 1-adrenoceptor agonists, phenylephrine and methoxamine, depressed the neuronal discharges of most of the units tested, while NE evoked both excitatory and inhibitory effects which were blocked by propranolol and phentolamine or prazosin, respectively. Imipramine, mianserin, (+)- and (-)-oxaprotiline administered subchronically (10 mg/kg p.o., twice daily for 14 days, withdrawal 48 h), potentiated the inhibitory reaction to phenylephrine. Mianserin was the only drug tested in the acute dose to effectively augment the reaction to alpha 1-adrenoceptor stimulation. Prolonged administration of mianserin and imipramine attenuated the excitatory effect to NE, which probably reflects beta-receptor down-regulation; however, only mianserin, but not imipramine, enhanced the NE-induced inhibition. The observed potentiation of the alpha 1-adrenoceptor-related inhibitory reaction to phenylephrine produced by antidepressant drugs may reflect the development of the alpha 1-adrenergic system supersensitivity in the hippocampus.

摘要

通过细胞外记录CA1层神经元的自发活动,研究了抗抑郁药物长期治疗对海马切片中去氧肾上腺素和去甲肾上腺素(NE)诱发反应的影响。α1 -肾上腺素能受体激动剂去氧肾上腺素和甲氧明抑制了大多数受试单位的神经元放电,而NE分别引起兴奋和抑制作用,这些作用分别被普萘洛尔和酚妥拉明或哌唑嗪阻断。亚慢性给予丙咪嗪、米安色林、(+)-和(-)-奥沙普明(10mg/kg口服,每日两次,共14天,停药48小时)可增强对去氧肾上腺素的抑制反应。米安色林是唯一在急性剂量下有效增强对α1 -肾上腺素能受体刺激反应的受试药物。长期给予米安色林和丙咪嗪可减弱对NE的兴奋作用,这可能反映了β受体下调;然而,只有米安色林而非丙咪嗪增强了NE诱导的抑制作用。抗抑郁药物对去氧肾上腺素产生的与α1 -肾上腺素能受体相关的抑制反应的增强,可能反映了海马中α1 -肾上腺素能系统超敏反应的发展。

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