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首页> 外文期刊>Psychopharmacology >The cannabinoid CB1 receptor antagonist SR141716A attenuates the memory impairment produced by delta9-tetrahydrocannabinol or anandamide.
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The cannabinoid CB1 receptor antagonist SR141716A attenuates the memory impairment produced by delta9-tetrahydrocannabinol or anandamide.

机译:大麻素CB1受体拮抗剂SR141716A可以减轻delta9-四氢大麻酚或anandamide产生的记忆障碍。

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The administration of delta9-tetrahydrocannabinol (THC), the principle psychoactive ingredient in marijuana, or the endogenous cannabinoid anandamide, has been shown to impair recent memory. The purpose of the present investigation was to determine if the cannabinoid CB1 receptor antagonist SR141716A could attenuate THC- or anandamide-induced memory impairment, and to assess the effects on memory of SR141716A alone. Memory was assessed in rats well-trained in a two-component instrumental discrimination task, consisting of a conditional discrimination, and a non-match-to-position to assess recent or working memory. SR141716A (0.0-2.0 mg/kg) had no effect on either the conditional discrimination or the non-match-to-position. However, SR141716A (0.0-2.0 mg/kg) attenuated the memory impairment produced by THC (2.0 or 4.0 mg/kg) as indexed by an enhancement of performance in the non-match-to-position. When administered to rats pretreated with anandamide (2.0 mg/kg), SR141716A (0.0-2.5 mg/kg) impaired performance in the conditional discrimination at the highest dose. This was interpreted as a deficit in some capacity unrelated to memory (e.g., motor impairment). However, lower doses of SR141716A (0.1 and 0.5 mg/kg) attenuated the anandamide-induced impairment of performance in the non-match-to-position without affecting the conditional discrimination. This is the first report that the memory impairment produced by anandamide can be attenuated by a cannabinoid antagonist; results suggest that anandamide-induced memory disruption is mediated by CB receptors.
机译:服用大麻中的主要精神活性成分delta9-tetrahydrocannabinol(THC)已证明会损害近期记忆。本研究的目的是确定大麻素CB1受体拮抗剂SR141716A是否可以减轻THC或anandamide引起的记忆障碍,并评估单独对SR141716A记忆的影响。在训练有素的大鼠中进行记忆训练,该训练包括两部分的仪器判别任务,包括条件判别和位置不匹配以评估近期或工作记忆。 SR141716A(0.0-2.0 mg / kg)对条件判别或位置不匹配均无影响。但是,SR141716A(0.0-2.0 mg / kg)减弱了THC(2.0或4.0 mg / kg)产生的记忆障碍,这是由于位置不匹配性能的增强所引起的。当对用anandamide(2.0 mg / kg)预处理的大鼠给药时,SR141716A(0.0-2.5 mg / kg)在最高剂量下有条件的辨别能力受损。这被解释为与记忆力无关的某些容量不足(例如,运动障碍)。但是,较低的SR141716A剂量(0.1和0.5 mg / kg)在不影响位置区分的情况下减弱了由anandamide诱导的性能丧失。这是第一个报道大麻素拮抗剂可以减轻由花生四烯酸产生的记忆障碍。结果表明,anandamide诱导的记忆破坏是由CB受体介导的。

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