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可卡因自我给药似乎是由多巴胺摄取抑制介导的。

Cocaine self-administration appears to be mediated by dopamine uptake inhibition.

作者信息

Ritz M C, Lamb R J, Goldberg S R, Kuhar M J

机构信息

National Institute on Drug Abuse, Addiction Research Center, Baltimore, Maryland.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1988;12(2-3):233-9. doi: 10.1016/0278-5846(88)90040-1.

Abstract
  1. While cocaine binds to several known sites in the brain, the binding site or receptor associated with its reinforcing or addictive properties has not been identified as such. 2. The identification of the pharmacologically relevant receptor(s) requires that an association exist between the potency of a variety of cocaine of cocaine-related drugs in animal models of substance and their potency at a binding site in the brain. 3. Our experiments indicate that the potencies of cocaine-like drugs in animal studies of drug self-administration are correlated with their potencies in inhibiting 3H-mazindol binding to dopamine transporters in the rat striatum. Cocaine binding to several other presynaptic and postsynaptic binding sites does not appear to be associated with the reinforcing effects of the drug. 4. Thus, the cocaine receptor related to substance abuse appears to be the binding site associated with inhibition of dopamine uptake on the dopaminergic nerve terminals.
摘要
  1. 虽然可卡因可与大脑中多个已知位点结合,但其与强化或成瘾特性相关的结合位点或受体尚未得到明确确认。2. 确定药理学相关受体需要在物质的动物模型中,多种可卡因及可卡因相关药物的效力与其在大脑结合位点的效力之间存在关联。3. 我们的实验表明,在药物自我给药的动物研究中,可卡因样药物的效力与其抑制大鼠纹状体中3H-马吲哚与多巴胺转运体结合的效力相关。可卡因与其他几个突触前和突触后结合位点的结合似乎与该药物的强化作用无关。4. 因此,与药物滥用相关的可卡因受体似乎是与抑制多巴胺能神经末梢上多巴胺摄取相关的结合位点。

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