Regulation of cannabinoid CB1 receptors in the central nervous system by chronic cannabinoids.

Laura J Sim-Selley
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引用次数: 243

Abstract

Marijuana produces a number of characteristic behaviors in humans and animals, including memory impairment, antinociception, and locomotor and psychoactive effects. However, tolerance and dependence to cannabinoids develops after chronic use, as demonstrated both clinically and in animal models. The potential therapeutic benefits of certain cannabinoid-mediated effects, as well as the use of marijuana for its psychoactive properties, has raised interest in understanding the cellular adaptations produced by chronic administration of this class of drugs. The primary active constituent of marijuana, delta9-tetrahydrohydrocannabinol (THC), binds to specific G-protein-coupled receptors. The central nervous system (CNS) effects of THC are mediated by CB1 receptors, which couple primarily to inhibitory G-proteins. High levels of CB1 receptors are found in the basal ganglia, hippocampus, cortex, and cerebellum, consistent with the profile of behavioral effects. Studies over the past decade have determined that CB1 receptors undergo downregulation and desensitization following chronic administration of THC or synthetic cannabinoid agonists. In general, these adaptations are regionally widespread and of considerable magnitude, and are thought to contribute to tolerance to cannabinoid-mediated behavioral effects. Adaptation at the effector level has been more difficult to characterize, although it appears that alterations in cyclic adenosine monophosphate (cAMP) and protein kinase A (PKA) activity may be particularly important in cannabinoid dependence. A striking characteristic of CB 1 receptor adaptation is the region dependence of the magnitude and rate of development of downregulation and desensitization. These regional differences may provide interesting insights into the mechanisms of CB1 receptors receptor signaling in different brain regions. Moreover, region-specific adaptations in CB1 receptors following chronic cannabinoid administration may produce differential adaptations at the in vivo level.

慢性大麻素对中枢神经系统大麻素CB1受体的调节。
大麻在人类和动物身上产生了许多特有的行为,包括记忆障碍、抗感觉、运动和精神作用。然而,正如临床和动物模型所证明的那样,对大麻素的耐受性和依赖性在长期使用后发展。某些大麻素介导作用的潜在治疗益处,以及大麻的精神活性特性的使用,引起了人们对理解这类药物长期服用所产生的细胞适应性的兴趣。大麻的主要活性成分δ 9-四氢氢大麻酚(THC)与特定的g蛋白偶联受体结合。四氢大麻酚对中枢神经系统(CNS)的作用由CB1受体介导,CB1受体主要与抑制性g蛋白偶联。在基底神经节、海马体、皮质和小脑中发现了高水平的CB1受体,这与行为效应的概况一致。过去十年的研究已经确定,长期服用四氢大麻酚或合成大麻素激动剂后,CB1受体会发生下调和脱敏。总的来说,这些适应在区域内广泛存在,而且规模相当大,被认为有助于对大麻素介导的行为影响的耐受性。尽管环磷酸腺苷(cAMP)和蛋白激酶A (PKA)活性的改变在大麻素依赖中可能特别重要,但效应水平的适应更难以表征。cb1受体适应的一个显著特征是下调和脱敏的发展幅度和速度的区域依赖性。这些区域差异可能为了解不同脑区CB1受体信号传导的机制提供了有趣的见解。此外,慢性大麻素给药后CB1受体的区域特异性适应可能在体内水平上产生差异适应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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