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抗抑郁药治疗对脑单胺能受体的不同影响。

Differential effects of antidepressant treatment on brain monoaminergic receptors.

作者信息

Maggi A, U'Prichard D C, Enna S J

出版信息

Eur J Pharmacol. 1980 Jan 25;61(2):91-8. doi: 10.1016/0014-2999(80)90152-1.

Abstract

Chronic (21 days) antidepressant administration to rats results in a decrease in both serotonin and beta-adrenergic, but not cholinergic muscarinic, receptor binding in selected brain regions, with the frontal cortex appearing to be somewhat more sensitive to this effect. Neither nisoxetine nor fluoxetine, potent and specific inhibitors of norepinephrine and serotonin uptake respectively, caused receptor binding changes after chronic administration, suggesting that inhibition of transmitter uptake, in itself, is insufficient to cause receptor subsensitivity. In vitro experiments indicated that antidepressants are relatively weak alpha 2-receptor blocking agents, but some are potent on the alpha 1-receptor system indicating that the norepinephrine releasing potency of some antidepressants may not be mediated by blockade of presynaptic autoreceptors.

摘要

对大鼠进行为期21天的慢性抗抑郁药给药后,特定脑区中血清素和β-肾上腺素能受体结合减少,但胆碱能毒蕈碱受体结合未减少,额叶皮质似乎对这种效应更为敏感。分别作为去甲肾上腺素和血清素摄取的强效特异性抑制剂的尼索西汀和氟西汀,在慢性给药后均未引起受体结合变化,这表明递质摄取的抑制本身不足以导致受体敏感性降低。体外实验表明,抗抑郁药是相对较弱的α2受体阻断剂,但有些对α1受体系统有强效作用,这表明一些抗抑郁药的去甲肾上腺素释放效力可能不是由突触前自身受体的阻断介导的。

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