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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Discriminative stimulus effects of the GABAB receptor-positive modulator rac-BHFF: Comparison with GABAB receptor agonists and drugs of abuse
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Discriminative stimulus effects of the GABAB receptor-positive modulator rac-BHFF: Comparison with GABAB receptor agonists and drugs of abuse

机译:GABAB受体阳性调节剂rac-BHFF的歧视性刺激效果:与GABAB受体激动剂和滥用药物的比较

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GABAB receptor-positive modulators are thought to have advantages as potential medications for anxiety, depression, and drug addiction. They may have fewer side effects than GABAB receptor agonists, because selective enhancement of activated receptors could have effects different from nonselective activation of all receptors. To examine this, pigeons were trained to discriminate the GABAB receptor-positive modulator (R,S)-5,7- di-tert-butyl-3-hydroxy-3-trifluoromethyl-3H-benzofuran-2- one (rac-BHFF) from its vehicle. The discriminative stimulus effects of rac-BHFF were not mimicked by the GABAB receptor agonists baclofen and g-hydroxybutyrate (GHB), not by diazepam, and not by alcohol, cocaine, and nicotine, whose selfadministration has been reported to be attenuated by GABAB receptor-positive modulators. The discriminative stimulus effects of rac-BHFF were not antagonized by the GABAB receptor antagonist 3-aminopropyl (diethoxymethyl)phosphinic acid (CGP35348) but were attenuated by the less efficacious GABAB receptor-positive modulator 2,6-di-tert-butyl-4-(3-hydroxy-2,2- dimethylpropyl)phenol (CGP7930), suggesting the possibility that rac-BHFF produces its discriminative stimulus effects by directly activating GABAB2 subunits of GABAB receptors. At a dose 10- fold lower than the training dose, rac-BHFF enhanced the discriminative stimulus effects of baclofen, but not of GHB. This study provides evidence that the effects of GABAB receptorpositive modulators are not identical to those of GABAB receptor agonists. In addition, the results suggest that positive modulation of GABAB receptors does not produce discriminative stimulus effects similar to those of benzodiazepines, alcohol, cocaine, and nicotine. Finally, the finding that rac-BHFF enhanced effects of baclofen but not of GHB is consistent with converging evidence that the populations of GABAB receptors mediating the effects of baclofen and GHB are not identical.
机译:GABA B受体阳性调节剂被认为具有作为焦虑,抑郁和药物成瘾的潜在药物的优势。它们可能比GABAB受体激动剂具有更少的副作用,因为活化受体的选择性增强作用可能不同于所有受体的非选择性活化作用。为了检验这一点,对鸽子进行了训练以区分GABAB受体阳性调节剂(R,S)-5,7-二叔丁基-3-羟基-3-三氟甲基-3H-苯并呋喃-2-一(rac-BHFF )。 GABAB受体激动剂巴氯芬和g-羟基丁酸酯(GHB),地西epa,酒精,可卡因和尼古丁均不能模仿rac-BHFF的歧视性刺激作用,据报道酒精,可卡因和尼古丁的自我给药已被GABAB受体减弱正调制器。 GABAB受体拮抗剂3-氨基丙基(二乙氧基甲基)次膦酸(CGP35348)并未拮抗rac-BHFF的歧视性刺激作用,但无效的GABA B受体阳性调节剂2,6-二叔丁基-4减弱了该作用。 -(3-羟基-2,2-二甲基丙基)苯酚(CGP7930),提示rac-BHFF通过直接激活GABAB受体的GABAB2亚基而产生歧视性刺激作用的可能性。 rac-BHFF的剂量比训练剂量低10倍,可增强巴氯芬的歧视性刺激作用,但不能增强GHB的歧视性刺激作用。这项研究提供了证据,表明GABAB受体阳性调节剂的作用与GABAB受体激动剂的作用不同。此外,结果表明,GABA B受体的正调节作用不会产生与苯二氮卓类,酒精,可卡因和尼古丁相似的歧视性刺激作用。最后,发现rac-BHFF增强了巴氯芬而不是GHB的作用,这与越来越多的证据表明,介导巴氯芬和GHB的作用的GABAB受体群体不完全相同。

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