Stella Nephi
Department of Pharmacology, Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195-7280, USA.
Glia. 2004 Dec;48(4):267-77. doi: 10.1002/glia.20084.
The cannabinoid signaling system is composed of cannabinoid (CB) receptors, their endogenous ligands, the endocannabinoids, and the enzymes that produce and inactivate them. It is well known that neurons communicate between each other through this signaling system. Delta 9-tetrahydrocannabinol, the main psychoactive compound of marijuana, interacts with CB receptors, impinging on this communication and inducing profound behavioral effects such as memory impairment and analgesia. Recent evidence suggests that glial cells also express components of the cannabinoid signaling system and marijuana-derived compounds act at CB receptors expressed by glial cells, affecting their functions. This review summarizes this evidence, discusses how glial cells might use the cannabinoid signaling system to communicate with neighboring cells, and argues that nonpsychotropic cannabinoids, both marijuana-derived and synthetic, likely constitute lead compounds for therapy aimed at reducing acute and chronic neuroinflammation, such as occurs in multiple sclerosis.
大麻素信号系统由大麻素(CB)受体、其内源性配体(即内源性大麻素)以及产生和使它们失活的酶组成。众所周知,神经元通过这个信号系统相互交流。大麻的主要精神活性化合物Δ9-四氢大麻酚与CB受体相互作用,影响这种交流并引发深刻的行为效应,如记忆损害和镇痛。最近的证据表明,胶质细胞也表达大麻素信号系统的成分,大麻衍生化合物作用于胶质细胞表达的CB受体,影响其功能。本综述总结了这一证据,讨论了胶质细胞如何利用大麻素信号系统与邻近细胞进行交流,并认为大麻衍生和合成的非精神活性大麻素可能构成旨在减轻急性和慢性神经炎症(如多发性硬化症中发生的炎症)的治疗先导化合物。