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全身或杏仁核内注射内源性大麻素CB1受体拮抗剂AM251可阻断丙泊酚诱导的顺行性遗忘。

Systemic or intra-amygdala infusion of an endocannabinoid CB1 receptor antagonist AM251 blocked propofol-induced anterograde amnesia.

作者信息

Ren Y, Wang J, Xu P B, Xu Y J, Miao C H

机构信息

Department of Anesthesiology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

Department of Anesthesiology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

出版信息

Neurosci Lett. 2015 Jan 1;584:287-91. doi: 10.1016/j.neulet.2014.11.001. Epub 2014 Nov 6.

Abstract

Propofol is well-known for its anterograde amnesic actions. However, a recent experiment showed that propofol can also produce retrograde memory enhancement effects via an interaction with the endocannabinoid CB1 system. Therefore, the authors hypothesized that the regulating effect of propofol on the endocannabinoid CB1 system might also decrease the anterograde amnesic effect of propofol under some conditions, which might be a risk factor for intraoperative awareness. Since, the basolateral amygdala (BLA) has been confirmed to mediate propofol-induced anterograde amnesia and the BLA contains a high concentration of CB1 receptors, the authors investigated whether and how the endocannabinoid system, particularly the CB1 receptor within BLA, influences propofol-induced anterograde amnesia. Male Sprague-Dawley rats trained with inhibitory avoidance (IA) were systematically pre-trained using a memory-impairing dose of propofol (25 mg/kg). Before propofol administration, rats received an intraperitoneal injection of a CB1 receptor antagonist AM251 (1 mg/kg or 2 mg/kg) or a bilateral intra-BLA injection of AM251 (0.6 ng or 6 ng per 0.5 μl). Twenty-four hours after IA training, the IA retention latency was tested. It was found that systemic or intra-BLA injection of a non-regulating dose of AM251 (2 mg/kg or 6 ng per 0.5 μl, respectively) blocked the memory-impairing effect of propofol. These results indicate that the anterograde amnesic effect of propofol is mediated, in part, by activation of the CB1 cannabinoid receptors in the BLA.

摘要

丙泊酚以其顺行性遗忘作用而闻名。然而,最近的一项实验表明,丙泊酚还可通过与内源性大麻素CB1系统相互作用产生逆行性记忆增强效应。因此,作者推测,在某些情况下,丙泊酚对内源性大麻素CB1系统的调节作用可能也会降低丙泊酚的顺行性遗忘效应,这可能是术中知晓的一个危险因素。由于基底外侧杏仁核(BLA)已被证实介导丙泊酚诱导的顺行性遗忘,且BLA中含有高浓度的CB1受体,作者研究了内源性大麻素系统,尤其是BLA内的CB1受体,是否以及如何影响丙泊酚诱导的顺行性遗忘。用抑制性回避(IA)训练的雄性Sprague-Dawley大鼠,使用记忆损害剂量的丙泊酚(25mg/kg)进行系统的预训练。在给予丙泊酚之前,大鼠腹腔注射CB1受体拮抗剂AM251(1mg/kg或2mg/kg)或双侧脑室内注射AM251(每0.5μl 0.6ng或6ng)。IA训练24小时后,测试IA保留潜伏期。结果发现,全身或脑室内注射非调节剂量的AM251(分别为2mg/kg或每0.5μl 6ng)可阻断丙泊酚的记忆损害效应。这些结果表明,丙泊酚的顺行性遗忘效应部分是由BLA中CB1大麻素受体的激活介导的。

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