Striatal dopamine autoreceptors uninfluenced by chronic administration of antidepressants.

Striatal dopamine autoreceptors uninfluenced by chronic administration of antidepressants.
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纹状体多巴胺自身受体不受长期服用抗抑郁药的影响。

DOI:
10.1016/0014-2999(82)90507-6
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发表时间:
1982
影响因子:
5
通讯作者:
Roth,RH
Roth,RH
中科院分区:
医学2区
文献类型:
--
作者:
Holcomb,HH;Bannon,MJ;Roth,RH

文献摘要

被引文献

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Dopamine (DA) receptor sensitivity to apomorphine (APO) was assessed in the rat nigrostriatal system following chronic antidepressant treatment. Imipramine (IMI), iprindole (IPR) or vehicle was administered to rats for 10 days (10 mg/kg i.p., b.i.d.). Two and a half days after the last injection 3,4-dihydroxyphenylacetic acid (DOPAC) levels were measured in rat striata following injection of APO (50 or 100 μg/kg s.c.) or vehicle. In contrast with rats receiving chronic vehicle injections, rats chronically treated with IMI or IPR failed to exhibit a significant APO-induced fall in striatal DOPAC levels. Antidepressant-treated animals, however, exhibited significantly lower basal DOPAC levels than vehicle-treated rats. In an effort to localize the diminished APO response, DA autoreceptor sensitivity to APO was assessed in drug- and vehicle-treated animals. Employing γ-butyrolactone (GBL) and a dihydroxyphenylalamine (DOPA) decarboxylase inhibitor to elevate striatal DOPA, the APO-induced reversal of DOPA elevation was used as an index of DA autoreceptor sensitivity. This GBL-stimulated in vivo tyrosine hydroxylation was similarly reversed by APO (125, 250 or 500 μg/kg i.p.) in IMI-, IPR- and vehicle-treated animals. In view of these findings, we propose that the blunted biochemical response to APO observed in animals pretreated with antidepressants does not originate as a result of alterations in the sensitivity of DA autoreceptors located on the striatal presynaptic nerve terminal.