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多巴胺摄取参与可卡因的辨别性刺激效应。

Involvement of dopamine uptake in the discriminative stimulus effects of cocaine.

作者信息

Broadbent J., Michael E.K., Riddle E.E., Apple J.B.

机构信息

Department of Physiology and Pharmacology, Bowman Gray School of Medicine, 300 South Hawthorne Rd, Winston-Salem, N.C. 27103 USA.

出版信息

Behav Pharmacol. 1991 Jun;2(3):187-197.

Abstract

The involvement of dopaminergic and adrenergic mechanisms in the stimulus effects of cocaine was studied in rats trained to discriminate cocaine from saline. The cocaine (10mg/kg) cue generalized to compounds that act primarily by inhibiting DA uptake with an order of potency of nomifensine (ED(50) = 0.38mg/kg) > GBR12909 (1-{2-[bis(4-fluorophenyl) methoxy]-ethyl]}-4(3-phenylpropyl) piperazine (ED(50) = 4.38mg/kg) > bupropion (ED(50) = 11.6mg/kg) but not to those that: (1) directly activate postsynaptic DA receptors (bromocriptine), (2) release DA (amantadine), (3) have antagonist actions at presynaptic DA receptors (cis-flupenthixol) or, (4) inhibit the uptake of NE (desipramine, imipramine, nisoxetine). When given in combination with cocaine, the D2 receptors antagonist (-)sulpiride had no significant effects on cocaine-lever selection. These results suggest that inhibition of DA uptake is involved in the discriminative stimulus properties of cocaine since, (1) compounds that act by inhibiting DA uptake rather than through some other mechanism mimic cocaine and, (2) the reported affinities of these drugs for the DA transport site and their order of potency in blocking cocaine are identical.

摘要

在训练大鼠区分可卡因和生理盐水的实验中,研究了多巴胺能和肾上腺素能机制在可卡因刺激效应中的作用。可卡因(10毫克/千克)线索可泛化至主要通过抑制多巴胺摄取起作用的化合物,其效力顺序为:诺米芬辛(半数有效剂量[ED(50)] = 0.38毫克/千克)> GBR12909(1-{2-[双(4-氟苯基)甲氧基]-乙基}-4(3-苯基丙基)哌嗪,ED(50) = 4.38毫克/千克)>安非他酮(ED(50) = 11.6毫克/千克),但不会泛化至以下化合物:(1)直接激活突触后多巴胺受体的药物(溴隐亭),(2)释放多巴胺的药物(金刚烷胺),(3)对突触前多巴胺受体有拮抗作用的药物(顺式氟哌噻吨),或(4)抑制去甲肾上腺素摄取的药物(地昔帕明、丙咪嗪、尼索西汀)。当与可卡因联合给药时,D2受体拮抗剂(-)舒必利对可卡因杠杆选择无显著影响。这些结果表明,抑制多巴胺摄取参与了可卡因的辨别刺激特性,因为:(1)通过抑制多巴胺摄取而非其他机制起作用的化合物可模拟可卡因,(2)这些药物对多巴胺转运位点的报道亲和力及其阻断可卡因的效力顺序是相同的。

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