首页> 外文期刊>European Journal of Pharmacology: An International Journal >WIN 55,212-2-induced reduction of cocaine hyperlocomotion: possible inhibition of 5-HT(3) receptor function.
【24h】

WIN 55,212-2-induced reduction of cocaine hyperlocomotion: possible inhibition of 5-HT(3) receptor function.

机译:WIN 55,212-2诱导减少可卡因运动过度:可能抑制5-HT(3)受体功能。

获取原文
获取原文并翻译 | 示例
           

摘要

We examined the effect of WIN 55,212-2 (an agonist of cannabinoid receptors) and its enantiomer WIN 55,212-3, as well as of ondansetron (an antagonist of serotonin (5-HT)(3) receptors) on the cocaine-induced locomotor hyperactivity in rats. WIN 55,212-2, but not WIN 55,212-3, in doses of 3 and 6 mg/kg which did not affect the basal locomotor activity, dose-dependently reduced the hyperactivation evoked by cocaine. The inhibitory effect of WIN 55,212-2 was not affected by rimonabant (an antagonist of cannabinoid receptors). Like in the case of WIN 55,212-2, the cocaine-induced hyperlocomotion was reduced in a dose-dependent manner by ondansetron (0.03-0.3 mg/kg). The obtained results indicate that the inhibitory effect of WIN 55,212-2 on cocaine hyperactivation is stereoselective and is not mediated by cannabinoid receptors. Moreover, together with the literature data they may suggest that this effect of WIN 55,212-2 involves inhibition of the 5-HT(3) receptor function.
机译:我们研究了WIN 55,212-2(大麻素受体激动剂)及其对映体WIN 55,212-3,以及恩丹西酮(5-羟色胺(5-HT)(3)受体的拮抗剂)对可卡因诱导的运动的影响大鼠活动过度。以3和6 mg / kg的剂量服用WIN 55,212-2,而不是WIN 55,212-3,不影响基础运动能力,剂量依赖性地降低了可卡因引起的过度激活。利莫那班(大麻素受体拮抗剂)不影响WIN 55,212-2的抑制作用。像WIN 55,212-2一样,可卡因诱导的过度运动通过恩丹西酮(0.03-0.3 mg / kg)以剂量依赖性方式降低。获得的结果表明,WIN 55,212-2对可卡因过度激活的抑制作用是立体选择性的,并且不受大麻素受体介导。此外,连同文献数据,他们可能暗示WIN 55,212-2的这种作用涉及对5-HT(3)受体功能的抑制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号