Ohno-Shosaku Takako, Kano Masanobu
Department of Impairment Study, Graduate School of Medical Science, Kanazawa University, Kanazawa 920-0942, Japan.
Department of Neurophysiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Curr Opin Neurobiol. 2014 Dec;29:1-8. doi: 10.1016/j.conb.2014.03.017. Epub 2014 Apr 18.
One of the two major endocannabinoids, 2-arachidonoylglycerol (2-AG), serves as a retrograde messenger at various types of synapses throughout the brain. Upon postsynaptic activation, 2-AG is released immediately after de novo synthesis, activates presynaptic CB1 cannabinoid receptors, and transiently suppresses neurotransmitter release. When CB1 receptor activation is combined with some other factors such as presynaptic activity, the suppression is converted to a long-lasting form. Whereas 2-AG primarily transmits a rapid, transient, point-to-point retrograde signal, the other major endocannabinoid, anandamide, may function as a relatively slow retrograde or non-retrograde signal or as an agonist of the vanilloid receptor. The endocannabinoid system can be up- or down-regulated by a variety of physiological and environmental factors including stress, which might be clinically important.
两种主要内源性大麻素之一的2-花生四烯酸甘油酯(2-AG),在整个大脑的各种突触中充当逆行信使。突触后激活时,2-AG在从头合成后立即释放,激活突触前CB1大麻素受体,并短暂抑制神经递质释放。当CB1受体激活与诸如突触前活动等其他一些因素相结合时,这种抑制会转变为持久形式。虽然2-AG主要传递快速、短暂、点对点的逆行信号,但另一种主要内源性大麻素花生四烯乙醇胺可能作为相对缓慢的逆行或非逆行信号,或作为香草酸受体的激动剂发挥作用。内源性大麻素系统可被包括应激在内的多种生理和环境因素上调或下调,这可能具有临床重要性。