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Neuropharmacology of the Endocannabinoid Signaling System-Molecular Mechanisms, Biological Actions and Synaptic Plasticity

机译:内源性大麻素信号传导系统的神经药理学-分子机制,生物学作用和突触可塑性

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The endocannabinoid signaling system is composed of the cannabinoid receptors; their endogenous ligands, the endocannabinoids; the enzymes that produce and inactivate the endocannabinoids; and the endocannabinoid transporters. The endocannabinoids are a new family of lipidic signal mediators, which includes amides, esters, and ethers of long-chain polyunsaturated fatty acids. Endocannabinoids signal through the same cell surface receptors that are targeted by Δ9-tetrahydrocannabinol (Δ9-THC), the active principles of cannabis sativa preparations like hashish and marijuana. The biosynthetic pathways for the synthesis and release of endocannabinoids are still rather uncertain. Unlike neurotransmitter molecules that are typically held in vesicles before synaptic release, endocannabinoids are synthesized on demand within the plasma membrane. Once released, they travel in a retrograde direction and transiently suppress presynaptic neurotransmitter release through activation of cannabinoid receptors. The endocannabinoid signaling system is being found to be involved in an increasing number of pathological conditions. In the brain, endocannabinoid signaling is mostly inhibitory and suggests a role for cannabinoids as therapeutic agents in central nervous system (CNS) disease. Their ability to modulate synaptic efficacy has a wide range of functional consequences and provides unique therapeutic possibilities. The present review is focused on new information regarding the endocannabinoid signaling system in the brain. First, the structure, anatomical distribution, and signal transduction mechanisms of cannabinoid receptors are described. Second, the synthetic pathways of endocannabinoids are discussed, along with the putative mechanisms of their release, uptake, and degradation. Finally, the role of the endocannabinoid signaling system in the CNS and its potential as a therapeutic target in various CNS disease conditions, including alcoholism, are discussed.
机译:内源性大麻素信号系统由大麻素受体组成。它们的内源性配体,内源性大麻素;产生和灭活大麻素的酶;和内源性大麻素转运蛋白。内源性大麻素是脂质信号介体的新家族,包括长链多不饱和脂肪酸的酰胺,酯和醚。内源性大麻素通过Δ9-四氢大麻酚(Δ9-THC)靶向的同一细胞表面受体发出信号,Δ9-四氢大麻酚(大麻的大麻素如大麻和大麻)的活性成分。内源性大麻素的合成和释放的生物合成途径仍然相当不确定。不同于通常在突触释放之前保留在囊泡中的神经递质分子,内源性大麻素是根据需要在质膜内合成的。一旦释放,它们便沿逆行方向行进并通过大麻素受体的激活而暂时抑制突触前神经递质的释放。发现内源性大麻素信号系统参与越来越多的病理状况。在大脑中,内源性大麻素信号传导主要具有抑制作用,表明大麻素作为中枢神经系统(CNS)疾病的治疗剂具有一定作用。它们调节突触功效的能力具有广泛的功能后果,并提供了独特的治疗可能性。目前的审查集中在有关大脑中的内源性大麻素信号系统的新信息。首先,描述了大麻素受体的结构,解剖分布和信号转导机制。其次,讨论了内源性大麻素的合成途径,以及其释放,摄取和降解的推测机制。最后,讨论了内源性大麻素信号系统在中枢神经系统中的作用及其在各种中枢神经系统疾病(包括酒精中毒)中作为治疗靶标的潜力。

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