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通过突触前大麻素受体调节递质释放。

Modulation of transmitter release via presynaptic cannabinoid receptors.

作者信息

Schlicker E, Kathmann M

机构信息

Institut für Pharmakologie und Toxikologie, Universität Bonn, Reuterstr. 2b, 53113, Bonn, Germany.

出版信息

Trends Pharmacol Sci. 2001 Nov;22(11):565-72. doi: 10.1016/s0165-6147(00)01805-8.

Abstract

Cannabis (marijuana) is not only a frequently abused drug but also has the potential for the development of useful agents for the treatment of emesis, anorexia and multiple sclerosis. In this article, the effects of modulation of transmitter release by cannabinoids in both the CNS and the PNS of various species, including humans, will be discussed. Cannabinoids inhibit neurotransmitter release via specific presynaptic cannabinoid CB1 receptors. Studies using either the CB1 receptor antagonist and inverse agonist SR141716 or CB1-receptor-deficient mice suggest that numerous presynaptic cannabinoid receptors are tonically activated by endogenous cannabinoids and/or are constitutively active. CB1-receptor-mediated inhibition of transmitter release might explain, for example, reinforcing properties and memory impairment caused by cannabinoids.

摘要

大麻( marijuana)不仅是一种经常被滥用的药物,而且具有开发用于治疗呕吐、厌食症和多发性硬化症的有用药物的潜力。在本文中,将讨论包括人类在内的各种物种的中枢神经系统和外周神经系统中,大麻素对递质释放的调节作用。大麻素通过特定的突触前大麻素CB1受体抑制神经递质释放。使用CB1受体拮抗剂和反向激动剂SR141716或CB1受体缺陷小鼠的研究表明,许多突触前大麻素受体被内源性大麻素持续激活和/或具有组成性活性。例如,CB1受体介导的对递质释放的抑制作用可能解释了大麻素引起的强化特性和记忆障碍。

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