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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Effects of nicotinic and NMDA receptor channel blockers on intravenous cocaine and nicotine self-administration in mice.
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Effects of nicotinic and NMDA receptor channel blockers on intravenous cocaine and nicotine self-administration in mice.

机译:烟碱和NMDA受体通道阻滞剂对小鼠静脉可卡因和尼古丁自我给药的影响。

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Previous studies have indicated that blockade of N-methyl-D-aspartate (NMDA) subtype of glutamate receptors prevents acquisition of instrumental behaviors reinforced by food and drugs such as morphine and cocaine. The present study aimed to extend this evidence by testing whether NMDA receptor channel blocker, memantine, would exert similar effects on acquisition of cocaine and nicotine self-administration in mice. Inasmuch as memantine also acts as nicotinic receptor channel blocker, this study assessed the effects of mecamylamine and MRZ 2/621 that are more selective nicotinic blockers. Adult male Swiss mice were allowed to self-administer cocaine (0.8-2.4 microg/infusion) or nicotine (0.08-0.32 microg/infusion) during the 30-min test. Pretreatment with memantine (0.1-10 mg/kg) prevented acquisition of nicotine but not cocaine self-administration. Pretreatment with mecamylamine (0.3-3 mg/kg) and MRZ 2/621 (0.3-10 mg/kg) produced dose-dependent suppression of both cocaine and nicotine self-administration. Taken together with the previous reports, these results indicate that nicotinic receptor blockers antagonize acute reinforcing effects of cocaine while NMDA receptor blockade may have limited effectiveness.
机译:先前的研究表明,谷氨酸受体的N-甲基-D-天冬氨酸(NMDA)亚型的阻断可阻止获得由食品和药物(例如吗啡和可卡因)增强的仪器行为。本研究旨在通过测试NMDA受体通道阻滞剂美金刚(manmantine)是否会在小鼠体内获得可卡因和尼古丁自我施用方面发挥类似作用,从而扩展这一证据。由于美金刚胺也起烟碱样受体通道阻滞剂的作用,因此本研究评估了美卡敏胺和MRZ 2/621的作用,后者是更具选择性的烟碱阻滞剂。在30分钟的测试中,允许成年雄性瑞士小鼠自行给予可卡因(0.8-2.4微克/滴注)或尼古丁(0.08-0.32微克/滴注)。美金刚胺(0.1-10 mg / kg)的预处理可预防获得尼古丁,但不能预防可卡因的自我给药。用美加明胺(0.3-3 mg / kg)和MRZ 2/621(0.3-10 mg / kg)进行预处理可卡因和尼古丁自我给药均产生剂量依赖性抑制作用。结合以前的报告,这些结果表明,烟碱样受体阻滞剂拮抗可卡因的急性增强作用,而NMDA受体阻滞作用可能有限。

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