McAllister K H, Pratt J A
Department of Physiology and Pharmacology, University of Strathclyde, Glasgow, UK.
Eur J Pharmacol. 1998 Jul 24;353(2-3):141-8. doi: 10.1016/s0014-2999(98)00405-1.
The tachykinin NK1 receptor antagonist, GR205171 ([2-methoxy-5-(5-trifluoromethyl-tetrazol-1-yl)-benzyl]-(2S-phenyl -piperidin-3S-yl)-amine), is a potent inhibitor of emesis induced by a wide variety of emetogens. This is in contrast to 5-HT3 (5-hydroxytryptamine3) receptor antagonists, such as ondansetron, which have a more restricted antiemetic profile. The present study evaluated the efficacy of GR205171, in comparison with ondansetron to block the acquisition of a conditioned taste aversion induced by either apomorphine (0.25 mg kg(-1) s.c.) or by amphetamine (0.5 mg kg(-1) s.c.) in rats. Pretreatment with GR205171 (0.1-1.0 mg kg(-1) s.c.) and ondansetron (0.001-0.1 mg kg(-1) s.c.) produced a dose-dependent blockade of conditioned taste aversions evoked by apomorphine. In contrast, the acquisition of conditioned taste aversions induced by amphetamine was inhibited by GR205171 (0.3-0.5 mg kg(-1) s.c.), but only attenuated by ondansetron (0.001-0.1 mg kg(-1) s.c.). These results suggest that tachykinin NK1 receptor antagonists may have potential in the treatment of drug-induced conditioned aversive behaviour and nausea.
速激肽NK1受体拮抗剂GR205171([2-甲氧基-5-(5-三氟甲基-四氮唑-1-基)-苄基]-(2S-苯基-哌啶-3S-基)-胺)是多种催吐剂诱发呕吐的强效抑制剂。这与5-HT3(5-羟色胺3)受体拮抗剂如昂丹司琼不同,后者的止吐作用更具局限性。本研究评估了GR205171与昂丹司琼相比,阻断阿扑吗啡(0.25 mg kg(-1)皮下注射)或苯丙胺(0.5 mg kg(-1)皮下注射)诱发的大鼠条件性味觉厌恶形成的效果。GR205171(0.1 - 1.0 mg kg(-1)皮下注射)和昂丹司琼(0.001 - 0.1 mg kg(-1)皮下注射)预处理对阿扑吗啡诱发的条件性味觉厌恶产生剂量依赖性阻断作用。相比之下,GR205171(0.3 - 0.5 mg kg(-1)皮下注射)可抑制苯丙胺诱发的条件性味觉厌恶形成,而昂丹司琼(0.001 - 0.1 mg kg(-1)皮下注射)仅使其减弱。这些结果表明,速激肽NK1受体拮抗剂在治疗药物诱发的条件性厌恶行为和恶心方面可能具有潜力。