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阿片类药物在动机过程中的双向作用及D1多巴胺受体的参与

Bidirectional effects of opioids in motivational processes and the involvement of D1 dopamine receptors.

作者信息

Herz A

机构信息

Department of Neuropharmacology, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, Federal Republic of Germany.

出版信息

NIDA Res Monogr. 1988;90:17-26.

PMID:2855853
Abstract

Exogenous and endogenous opioids significantly affect motivational processes; depending on the particular opioid receptor type with which they interact opposite effects are induced: activation of mu and delta opioid receptors is rewarding whereas activation of kappa opioid receptors induces aversive effects. Antagonism of mu-opioid receptors also induces aversion, suggesting the existence of a tonically active opioidergic reward pathway. There is evidence that beta-endorphin pathways arising from the hypothalamus play an important role in this respect. Opioid-induced reward as well as aversion seem to be mediated by the mesolimbic dopamine system, reward by increased, aversion by decreased transmission at D1 dopamine receptors.

摘要

外源性和内源性阿片类物质显著影响动机过程;根据它们相互作用的特定阿片受体类型,会产生相反的效应:μ和δ阿片受体的激活是奖赏性的,而κ阿片受体的激活则诱导厌恶效应。μ阿片受体的拮抗也会诱导厌恶,这表明存在一条持续活跃的阿片能奖赏通路。有证据表明,源自下丘脑的β-内啡肽通路在这方面发挥着重要作用。阿片类物质诱导的奖赏以及厌恶似乎都由中脑边缘多巴胺系统介导,奖赏是通过增加D1多巴胺受体处的传递,厌恶则是通过减少传递。

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1
Bidirectional effects of opioids in motivational processes and the involvement of D1 dopamine receptors.阿片类药物在动机过程中的双向作用及D1多巴胺受体的参与
NIDA Res Monogr. 1988;90:17-26.
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Examination of the neurochemical substrates mediating the motivational effects of opioids: role of the mesolimbic dopamine system and D-1 vs. D-2 dopamine receptors.介导阿片类药物动机效应的神经化学底物研究:中脑边缘多巴胺系统以及D-1与D-2多巴胺受体的作用
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Mu- and delta-opioid receptors inhibitorily linked to dopamine-sensitive adenylate cyclase in rat striatum display a selectivity profile toward endogenous opioid peptides different from that of presynaptic mu, delta and kappa receptors.在大鼠纹状体中,与多巴胺敏感的腺苷酸环化酶呈抑制性连接的μ和δ阿片受体,对内源性阿片肽的选择性谱不同于突触前μ、δ和κ受体。
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Differences among mouse strains in the regulation by mu, delta 1 and delta 2 opioid receptors of striatal adenylyl cyclases activated by dopamine D1 or adenosine A2a receptors.小鼠品系之间在由μ、δ1和δ2阿片受体对由多巴胺D1或腺苷A2a受体激活的纹状体腺苷酸环化酶的调节方面的差异。
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Opioid reward mechanisms: a key role in drug abuse?阿片类药物奖赏机制:在药物滥用中起关键作用?
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Opioid abuse and brain gene expression.阿片类药物滥用与大脑基因表达。
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The highly selective dopamine DR antagonist, R-VK4-40 attenuates oxycodone reward and augments analgesia in rodents.高度选择性的多巴胺 DR 拮抗剂 R-VK4-40 可减弱阿片类药物(如羟考酮)的奖赏效应,并增强其镇痛作用。
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Evaluation of the interaction of mu and kappa opioid agonists on locomotor behavior in the horse.μ和κ阿片受体激动剂对马运动行为的相互作用评估。
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