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慢性抗抑郁药治疗可下调大鼠额叶皮质中因急性应激而诱导的c-fos mRNA。

Chronic antidepressant treatment down-regulates the induction of c-fos mRNA in response to acute stress in rat frontal cortex.

作者信息

Morinobu S, Nibuya M, Duman R S

机构信息

Department of Psychiatry and Pharmacology, Connecticut Mental Health Center 06508, USA.

出版信息

Neuropsychopharmacology. 1995 May;12(3):221-8. doi: 10.1016/0893-133X(94)00067-A.

DOI:10.1016/0893-133X(94)00067-A
PMID:7612155
Abstract

The present study examines the influence of electroconvulsive seizure (ECS), as well as several antidepressant drug treatments, on the induction of c-fos mRNA in response to acute restraint stress. Acute (45-minute) restraint stress resulted in five- to sixfold elevation of c-fos mRNA levels in rat frontal cortex. Chronic administration of ECS significantly decreased the induction of c-fos mRNA levels in response to acute restraint stress, and this effect was observed after chronic (6 to 9 days) but not acute (1 or 3 days) of ECS treatment. In addition, c-fos induction in response to acute restraint stress was down-regulated by chronic, but not acute, administration of tranylcypromine or imipramine, two drugs that nonselectively increase synaptic levels of norepinephrine and serotonin by inhibition of monoamine oxidase or neurotransmitter reuptake, respectively. Moreover, chronic administration of desipramine or sertraline, selective re-uptake inhibitors of norepinephrine, or serotonin, respectively, also significantly down-regulated the induction of c-fos mRNA in response to restraint stress. Chronic administration of ECS, tranylcypromine, or imipramine also decreased stressed-induced levels of NGFI-A mRNA, another immediate early gene transcription factor, whereas levels of c-jun mRNA were not influenced by either stress or antidepressant treatments. The results demonstrate that chronic, but not acute, administration of ECS and several different classes of antidepressant drugs down-regulates stress-induced levels of c-fos mRNA, suggesting that this effect may be a common, postreceptor action of antidepressant treatments.

摘要

本研究考察了电惊厥发作(ECS)以及几种抗抑郁药物治疗对急性束缚应激诱导的c-fos mRNA表达的影响。急性(45分钟)束缚应激导致大鼠额叶皮质中c-fos mRNA水平升高5至6倍。慢性给予ECS可显著降低急性束缚应激诱导的c-fos mRNA水平,且这种效应在慢性(6至9天)而非急性(1或3天)ECS治疗后观察到。此外,慢性而非急性给予反苯环丙胺或丙咪嗪可下调急性束缚应激诱导的c-fos表达,这两种药物分别通过抑制单胺氧化酶或神经递质再摄取非选择性地增加去甲肾上腺素和5-羟色胺的突触水平。而且,慢性给予地昔帕明或舍曲林,分别为去甲肾上腺素或5-羟色胺的选择性再摄取抑制剂,也显著下调了束缚应激诱导的c-fos mRNA表达。慢性给予ECS、反苯环丙胺或丙咪嗪还降低了应激诱导的NGFI-A mRNA水平,NGFI-A是另一种即刻早期基因转录因子,而c-jun mRNA水平不受应激或抗抑郁治疗的影响。结果表明,慢性而非急性给予ECS和几种不同类别的抗抑郁药物可下调应激诱导的c-fos mRNA水平,提示这种效应可能是抗抑郁治疗常见的受体后作用。

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