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可卡因与假定的变构多巴胺转运体配体 SRI-31142 之间的相互作用。

Interactions between Cocaine and the Putative Allosteric Dopamine Transporter Ligand SRI-31142.

机构信息

Departments of Pharmacology and Toxicology (M.J.M., M.L.B., K.C.F., A.R.J., S.S.N.) and Physiology and Biophysics (J.M.E., T.W.E.S.), Virginia Commonwealth University, Richmond, Virginia; and Chemistry Department, Drug Discovery Division, Southern Research, Birmingham, Alabama (S.A., S.K.S.).

Departments of Pharmacology and Toxicology (M.J.M., M.L.B., K.C.F., A.R.J., S.S.N.) and Physiology and Biophysics (J.M.E., T.W.E.S.), Virginia Commonwealth University, Richmond, Virginia; and Chemistry Department, Drug Discovery Division, Southern Research, Birmingham, Alabama (S.A., S.K.S.)

出版信息

J Pharmacol Exp Ther. 2018 Nov;367(2):222-233. doi: 10.1124/jpet.118.250902. Epub 2018 Aug 27.

Abstract

Drugs that inhibit the dopamine (DA) transporter (DAT) include both therapeutic agents and abused drugs. Recent studies identified a novel series of putative allosteric DAT inhibitors, but the in vivo effects of these compounds are unknown. This study examined the abuse-related behavioral and neurochemical effects produced in rats by SRI-31142 [2-(7-methylimidazo[1,2-a]pyridin-6-yl)-N-(2-phenyl-2-(pyridin-4-yl)ethyl)quinazolin-4-amine], one compound from this series. In behavioral studies, intracranial self-stimulation (ICSS) was used to compare the effects produced by SRI-31142, the abused and nonselective DAT inhibitor cocaine, and the selective DAT inhibitor GBR-12935 [1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine]. In neurochemical studies, in vivo microdialysis was used to compare the effects of SRI-31142 and cocaine on levels of DA and serotonin in nucleus accumbens (NAc). The effects of SRI-31142 in combination with cocaine were also examined in both procedures. In contrast to cocaine and GBR-12935, SRI-31142 failed to produce abuse-related increases in ICSS or NAc DA; instead, SRI-31142 only decreased ICSS and NAc DA at a dose that was also sufficient to block cocaine-induced increases in ICSS and NAc DA. Pharmacokinetic studies suggested low but adequate brain penetration of SRI-31142, in vitro binding studies failed to identify likely non-DAT targets, and in vitro functional assays failed to confirm DA uptake inhibition in an assay of DAT-mediated fluorescent signals in live cells. These results indicate that SRI-31142 does not produce cocaine-like abuse-related effects in rats. SRI-31142 may have utility to block cocaine effects and may warrant further study as a candidate pharmacotherapy; however, the role of DAT in mediating these effects is unclear, and side effects may be a limiting factor.

摘要

抑制多巴胺(DA)转运蛋白(DAT)的药物包括治疗药物和滥用药物。最近的研究确定了一系列新的假定变构 DAT 抑制剂,但这些化合物的体内效应尚不清楚。本研究检查了 SRI-31142 [2-(7-甲基咪唑并[1,2-a]吡啶-6-基)-N-(2-苯基-2-(吡啶-4-基)乙基)喹唑啉-4-胺]在大鼠中的与滥用相关的行为和神经化学效应,这是该系列中的一种化合物。在行为研究中,颅内自我刺激(ICSS)用于比较 SRI-31142、滥用和非选择性 DAT 抑制剂可卡因以及选择性 DAT 抑制剂 GBR-12935 [1- [2-(二苯甲氧基)乙基]-4-(3-苯基丙基)哌嗪]产生的作用。在神经化学研究中,使用体内微透析比较 SRI-31142 和可卡因对伏隔核(NAc)中 DA 和 5-羟色胺水平的影响。还在这两种程序中检查了 SRI-31142 与可卡因联合使用的效果。与可卡因和 GBR-12935 相反,SRI-31142 未能在 ICSS 或 NAc DA 中产生与滥用相关的增加;相反,SRI-31142 仅在足以阻断可卡因诱导的 ICSS 和 NAc DA 增加的剂量下降低 ICSS 和 NAc DA。药代动力学研究表明 SRI-31142 有低但足够的脑穿透,体外结合研究未能确定可能的非 DAT 靶点,体外功能测定未能在活细胞中 DAT 介导的荧光信号测定中确认 DA 摄取抑制。这些结果表明 SRI-31142 不会在大鼠中产生可卡因样的与滥用相关的作用。SRI-31142 可能具有阻断可卡因作用的效用,并且可能值得进一步研究作为候选药物治疗;然而,DAT 在介导这些作用中的作用尚不清楚,并且副作用可能是一个限制因素。

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