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条件性应激增强大鼠前额叶皮质多巴胺释放的证据:探索地西泮和5-羟色胺1A受体激动剂的影响。

Evidence that conditioned stress enhances outflow of dopamine in rat prefrontal cortex: a search for the influence of diazepam and 5-HT1A agonists.

作者信息

Wedzony K, Maćkowiak M, Fijał K, Gołembiowska K

机构信息

Institute of Pharmacology, Polish Academy of Sciences, Krakøw, Poland.

出版信息

Synapse. 1996 Nov;24(3):240-7. doi: 10.1002/(SICI)1098-2396(199611)24:3<240::AID-SYN6>3.0.CO;2-E.

Abstract

We evaluated the impact of conditioned stress on outflow of dopamine in the rat prefrontal cortex. Exposure of rats to an environment associated with aversive stimuli-foot shock enhanced outflow of dopamine in a similar way as seen during the conditioning session when foot shocks were applied. Diazepam (2.5 and 10 mg/kg) dose-dependently decreased outflow of dopamine and, when given in a dose of 10 mg/kg, but not 2.5 mg/kg, decreased enhanced dopamine outflow evoked by conditioned stress. On the other hand, ipsapirone (10 mg/kg, but not 2.5 mg/kg) and buspirone (2.5 mg/kg) enhanced basal outflow of dopamine. When ipsapirone (10 mg/kg) and buspirone (2.5 mg/kg) were given to rats exposed to conditioned stress, the stress-evoked elevation in dopamine outflow was abolished. Ipsapirone in a dose of 2.5 mg/kg was ineffective in the stress paradigm tested. It is concluded that conditioned stress in vivo enhances dopaminergic neurotransmission in the rat prefrontal cortex, this effect being attenuated by diazepam, a classic anxiolytic drug, and by such novel anxiolytics as ipsapirone and buspirone, which operate via serotonergic 5-HT1A receptors. Although ipsapirone and buspirone blocked stress-induced enhancement of dopamine outflow, this effect seems to result from their influence on the basal outflow of dopamine. Differential effects of diazepam and 5-HT1A agonists on basal and stress-induced alterations in dopamine outflow are discussed in terms of their possible effectiveness in various types of general anxiety disorders.

摘要

我们评估了条件性应激对大鼠前额叶皮质多巴胺释放的影响。将大鼠暴露于与厌恶性刺激(足部电击)相关的环境中,可增强多巴胺的释放,其方式与在施加足部电击的条件反射训练期间观察到的相似。地西泮(2.5和10毫克/千克)剂量依赖性地降低多巴胺的释放,当给予10毫克/千克剂量时,但不是2.5毫克/千克剂量时,可降低由条件性应激诱发的多巴胺释放增强。另一方面, ipsapirone(10毫克/千克,但不是2.5毫克/千克)和丁螺环酮(2.5毫克/千克)可增强多巴胺的基础释放。当给暴露于条件性应激的大鼠给予ipsapirone(10毫克/千克)和丁螺环酮(2.5毫克/千克)时,应激诱发的多巴胺释放升高被消除。2.5毫克/千克剂量的ipsapirone在测试的应激范式中无效。得出的结论是,体内条件性应激增强大鼠前额叶皮质的多巴胺能神经传递,这种作用被经典抗焦虑药地西泮以及通过5-羟色胺能5-HT1A受体起作用的新型抗焦虑药ipsapirone和丁螺环酮所减弱。尽管ipsapirone和丁螺环酮阻断了应激诱导的多巴胺释放增强,但这种作用似乎是由于它们对多巴胺基础释放的影响。根据地西泮和5-HT1A激动剂在各种类型的广泛性焦虑症中的可能有效性,讨论了它们对多巴胺释放基础和应激诱导变化的不同影响。

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