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对大鼠重复给予HA - 966和氟哌啶醇:HA - 966激发后对纹状体多巴胺积累的耐受性相似,但对纹状体[3H]司哌罗宁结合的影响不同。

Repeated administration of HA-966 and haloperidol to rats: similar tolerance to striatal dopamine accumulation after HA-966 challenge, but dissimilar effects on striatal [3H]spiperone binding.

作者信息

Van der Krogt J A, Van Valkenburg C F, Belfroid R D, Heerkens C B

机构信息

Department of Pharmacology, Medical Faculty, University of Leiden, The Netherlands.

出版信息

Eur J Pharmacol. 1988 Dec 6;158(1-2):29-35. doi: 10.1016/0014-2999(88)90249-x.

Abstract

Repeated administration of 1-hydroxy-3-amino-pyrrolidone-2 (HA-966) to rats induces tolerance, as shown by a decreased, drug-stimulated accumulation of dopamine (DA) in the striatum. In the present study we compared the adaptive response of the striatal dopaminergic system to repeated administration of HA-966 with the adaptive response observed after repeated haloperidol. These treatments deprive dopamine (DA) receptors from their agonist and cause a blockade of DA receptors, respectively. Tolerance to HA-966 was not accompanied by a change in the specific binding of [3H]spiperone to striatal membranes. This is in contrast to the well-documented up-regulation of DA receptors that occurs with tolerance to haloperidol. Repeated haloperidol pretreatment also diminished DA accumulation following a challenge dose of HA-966, to a similar extent as that caused by repeated pretreatment with HA-966. These similar effects of pretreatment with HA-966 or haloperidol on the response to the HA-966 challenge are in line with, and strengthen, the idea that an increased sensitivity of presynaptic DA receptors is responsible for the decreasing effect of HA-966 after its repeated administration. Haloperidol and HA-966 clearly have different effects on postsynaptic DA receptors, as is shown by their differential effects on striatal [3H]spiperone binding.

摘要

对大鼠反复给予1-羟基-3-氨基-吡咯烷酮-2(HA-966)会诱导耐受性,这表现为纹状体中多巴胺(DA)受药物刺激的蓄积减少。在本研究中,我们比较了纹状体多巴胺能系统对反复给予HA-966的适应性反应与反复给予氟哌啶醇后观察到的适应性反应。这些处理分别使多巴胺(DA)受体失去其激动剂并导致DA受体的阻断。对HA-966的耐受性并未伴随着[3H]螺哌隆与纹状体膜特异性结合的变化。这与对氟哌啶醇耐受性出现时记录在案的DA受体上调形成对比。反复给予氟哌啶醇预处理也会使给予HA-966激发剂量后的DA蓄积减少,减少程度与反复给予HA-966预处理所导致的相似。HA-966或氟哌啶醇预处理对HA-966激发反应的这些相似作用与下述观点一致并强化了该观点,即突触前DA受体敏感性增加是HA-966反复给药后其作用减弱的原因。氟哌啶醇和HA-966对突触后DA受体显然有不同作用,这从它们对纹状体[3H]螺哌隆结合的不同影响可以看出。

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