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多巴胺D1样和D2样受体激动剂对恒河猴海洛因和可卡因自我给药行为的调节作用

Modulation of heroin and cocaine self-administration by dopamine D1- and D2-like receptor agonists in rhesus monkeys.

作者信息

Rowlett James K, Platt Donna M, Yao Wei-Dong, Spealman Roger D

机构信息

New England Primate Research Center, Harvard Medical School, Box 9102, One Pine Hill Dr., Southborough, MA 01772-9102, USA.

出版信息

J Pharmacol Exp Ther. 2007 Jun;321(3):1135-43. doi: 10.1124/jpet.107.120766. Epub 2007 Mar 9.

Abstract

Cocaine-heroin combinations ("speedballs") are commonly self-administered by polydrug abusers. Speedball self-administration may reflect in part an enhancement of the reinforcing effects of the drug combination compared with either drug alone. The present study investigated the degree to which the dopamine receptor system plays a role in cocaine-induced enhancement of heroin self-administration. In rhesus monkeys trained under a progressive ratio schedule of i.v. drug injection, combining heroin with cocaine shifted the heroin dose-response function leftward, and isobolographic analysis indicated that the combined effects were dose-additive. Likewise, combining heroin with the D1-like receptor agonists 6-chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepine HCl (SKF 81297) and 6-chloro-N-allyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-[1H]-3-benzazepine (SKF 82958) resulted in a leftward shift in the heroin dose-response function that was dose-additive. In contrast, combining heroin with the D2-like agonists R-(-)-propylnorapomorphine (NPA) and quinpirole shifted the heroin dose-response function to the right. Isobolographic analysis of the combined effects of heroin with NPA and quinpirole revealed infra-additive interactions in both cases. When combined with cocaine instead of heroin, both the D1-like receptor agonist SKF 81297 and the D2-like receptor agonist NPA enhanced cocaine self-administration. The combinations of SKF 81297 with cocaine were dose additive; however, the NPA-cocaine interaction was infra-additive. Together, the results suggest that D1- and D2-like receptor mechanisms may play qualitatively different roles in the combined self-administration of heroin and cocaine. In particular, stimulation of D1-like receptors enhances self-administration of heroin or cocaine individually, similar to the effects of combining cocaine with heroin, whereas stimulation of D2-like receptors seems to play primarily an inhibitory role.

摘要

可卡因-海洛因混合物(“速球”)通常被多种药物滥用者自行使用。自行使用“速球”可能部分反映出与单独使用任何一种药物相比,该药物组合的强化作用有所增强。本研究调查了多巴胺受体系统在可卡因诱导的海洛因自行使用增强中所起作用的程度。在恒河猴身上进行静脉注射药物的累进比率程序训练时,将海洛因与可卡因联合使用使海洛因剂量-反应函数向左移动,等效应线分析表明联合效应是剂量相加的。同样,将海洛因与D1样受体激动剂6-氯-7,8-二羟基-1-苯基-2,3,4,5-四氢-(1H)-3-苯并氮杂卓盐酸盐(SKF 81297)和6-氯-N-烯丙基-7,8-二羟基-1-苯基-2,3,4,5-四氢-[1H]-3-苯并氮杂卓(SKF 82958)联合使用,导致海洛因剂量-反应函数向左移动,且是剂量相加的。相比之下,将海洛因与D2样激动剂R-(-)-丙基去甲阿朴吗啡(NPA)和喹吡罗联合使用使海洛因剂量-反应函数向右移动。对海洛因与NPA和喹吡罗联合效应的等效应线分析在两种情况下均显示为次相加相互作用。当与可卡因而非海洛因联合使用时,D1样受体激动剂SKF 81297和D2样受体激动剂NPA均增强了可卡因的自行使用。SKF 81297与可卡因的组合是剂量相加的;然而,NPA-可卡因相互作用是次相加的。总之,结果表明D1样和D2样受体机制在海洛因和可卡因联合自行使用中可能发挥性质不同的作用。特别是,刺激D1样受体分别增强海洛因或可卡因的自行使用,类似于可卡因与海洛因联合使用的效果,而刺激D2样受体似乎主要起抑制作用。

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