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多巴胺和5-羟色胺受体敏感性与新纹状体多巴胺或5-羟色胺含量不相关。

Dopamine and 5-HT receptor sensitivity does not correlate with neostriatal dopamine or 5-HT content.

作者信息

Kostrzewa R M, Brus R, Perry K W, Fuller R W

机构信息

Department of Pharmacology, Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0577, USA.

出版信息

Acta Neurobiol Exp (Wars). 1996;56(1):21-8. doi: 10.55782/ane-1996-1099.

Abstract

To explore associations of neostriatal (NST) endogenous levels of dopamine (DA) and serotonin (5-HT) with sensitivity of their receptors, graded doses of 6-hydroxydopamine HBr (0 to 400 micrograms, ICV; 6-OHDA; desipramine pretreatment, 20 mg/kg IP) were given to rats between birth (P 0) and P 42. Numbers of vacuous chewing movements (VCMs) induced by SKF 38393 or m-chlorophenylpiperazine (m-CPP), respective DA D1 and 5-HT2 agonists, were subsequently determined. Enhanced SKF 38393-induced VCMs occurred when NST DA was reduced 97%-98% by high dose 6-OHDA (100-134 micrograms) at P 0 or P 3, but not in rats with 95%-97% loss in DA produced by 6-OHDA at P7 (134 micrograms) or P3 (67 micrograms). Enhanced m-CPP-induced VCMs occurred even when NST 5-HT content was not elevated after 6-OHDA (134 micrograms at P 10). Accordingly, D1 and 5-HT receptor sensitivity is not correlated with respective NST DA and 5-HT contents. The stage of ontogeny at the time of DA denervation may be the governing influence on receptor sensitivity.

摘要

为探究新纹状体(NST)内源性多巴胺(DA)和5-羟色胺(5-HT)水平与其受体敏感性之间的关联,在出生(P0)至P42期间给大鼠注射不同剂量的氢溴酸6-羟基多巴胺(0至400微克,脑室内注射;6-OHDA;预先腹腔注射20毫克/千克去甲丙咪嗪)。随后测定分别由DA D1和5-HT2激动剂SKF 38393或间氯苯哌嗪(m-CPP)诱导的空嚼运动(VCM)数量。当在P0或P3时通过高剂量6-OHDA(100 - 134微克)使NST DA减少97% - 98%时,SKF 38393诱导的VCM增强,但在P7(134微克)或P3(67微克)时由6-OHDA导致DA损失95% - 97%的大鼠中未出现这种情况。即使在P10时给予6-OHDA(134微克)后NST 5-HT含量未升高,m-CPP诱导的VCM也会增强。因此,D1和5-HT受体敏感性与各自的NST DA和5-HT含量不相关。DA去神经支配时的个体发育阶段可能是影响受体敏感性的主要因素。

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