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单独及联合使用地昔帕明和氟西汀长期治疗后大鼠脑中5-羟色胺2和β-肾上腺素能受体的调节

5-Hydroxytryptamine2 and beta-adrenergic receptor regulation in rat brain following chronic treatment with desipramine and fluoxetine alone and in combination.

作者信息

Goodnough D B, Baker G B

机构信息

Department of Psychiatry, University of Alberta, Edmonton, Canada.

出版信息

J Neurochem. 1994 Jun;62(6):2262-8. doi: 10.1046/j.1471-4159.1994.62062262.x.

DOI:10.1046/j.1471-4159.1994.62062262.x
PMID:8189233
Abstract

A chronic (14-day) study was initiated to investigate the effects of combined fluoxetine (FLU) and desipramine (DMI) treatment on the densities and affinities of beta-adrenergic and 5-hydroxytryptamine2 (5-HT2) receptors. Male Sprague-Dawley rats were administered the following doses using osmotic minipumps: FLU, 10 mg/kg/day; DMI, 5, 10, or 15 mg/kg/day; FLU, 10 mg/kg/day, plus DMI, 5 mg/kg/day; or vehicle (distilled water). After 14 days the cortex was dissected out and used for [3H]-ketanserin (5-HT2) binding, [3H]CGP-12177 (beta-adrenergic) binding, and drug level analysis. All animals receiving DMI showed significant down-regulation of 5-HT2 receptors except those receiving FLU in combination. DMI down-regulated beta-adrenergic receptors in a dose-dependent manner, with significantly greater down-regulation seen with the combination than with DMI (5 mg/kg/day) alone. This latter effect was apparently the result of greater levels of DMI in cortex with the combination than with DMI (5 mg/kg/day) alone. FLU had no effect on 5-HT2 or beta-adrenergic receptors on its own. Coadministration of FLU and DMI resulted in a doubling of levels of FLU and its demethylated metabolite, norfluoxetine (NFLU), and a tripling of DMI levels compared with values observed when FLU (10 mg/kg/day) or DMI (5 mg/kg/day) was administered alone.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

开展了一项为期14天的慢性研究,以调查氟西汀(FLU)和地昔帕明(DMI)联合治疗对β-肾上腺素能受体和5-羟色胺2(5-HT2)受体的密度及亲和力的影响。使用渗透微型泵给雄性斯普拉-道利大鼠施用以下剂量:氟西汀,10毫克/千克/天;地昔帕明,5、10或15毫克/千克/天;氟西汀,10毫克/千克/天加地昔帕明,5毫克/千克/天;或赋形剂(蒸馏水)。14天后,取出皮质用于[3H] - 酮舍林(5-HT2)结合、[3H]CGP - 12177(β-肾上腺素能)结合及药物水平分析。除联合使用氟西汀的动物外,所有接受地昔帕明的动物均显示5-HT2受体显著下调。地昔帕明以剂量依赖性方式下调β-肾上腺素能受体,联合使用时的下调程度明显大于单独使用地昔帕明(5毫克/千克/天)时。后一种效应显然是联合使用时皮质中地昔帕明水平高于单独使用地昔帕明(5毫克/千克/天)时的结果。氟西汀单独使用时对5-HT2或β-肾上腺素能受体无影响。与单独施用氟西汀(10毫克/千克/天)或地昔帕明(5毫克/千克/天)时观察到的值相比,氟西汀和地昔帕明联合给药导致氟西汀及其去甲基代谢产物去甲氟西汀(NFLU)的水平加倍,地昔帕明水平增至三倍。(摘要截短于250字)

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