R. Ngo
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引用次数: 4

摘要

本文探讨了内源性大麻素分子作为治疗创伤性脑损伤(TBI)的治疗方法的潜在用途。使用Google Scholar获取本综述分析的主要研究文献。通过给药2-AG或AEA配体、抑制分解酶以及使用CB1和CB2激动剂或拮抗剂等方法操纵内源性大麻素系统的研究显示,在治疗TBI方面有希望的结果;然而,迄今尚未发现实用的临床治疗方法。类似分子和受体的发现导致内源性系统的扩展,并产生了内源性大麻素组(endocannabinoidome)这个术语,它包含了新发现的分子和受体。内源性大麻素组的配体对TBI产生类似的治疗效果,但通过不同的受体途径起作用,这可能允许人们克服目前存在的操纵内源性大麻素系统治疗TBI的问题。目前,用于治疗创伤性脑损伤的疗法有许多不想要的副作用,因此需要进行替代研究。本文研究了先前研究的用于治疗TBI的三种内源性大麻素分子,并阐明了它们的特定受体途径,以及这些受体途径如何与内源性大麻素系统的普通途径不同。了解内源性大麻素组分子所使用的受体途径将为创伤性脑损伤的治疗开辟一个新的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Endocannabinoidome
This paper explores the potential use of endocannabinoidome molecules as a therapeutic approach to treating traumatic brain injury (TBI). Google Scholar was used to obtain the primary research literature analyzed for this review. Studies which manipulate the endocannabinoid system through methods such as administration of 2-AG or AEA ligands, inhibiting breakdown enzymes, and using CB1 and CB2 agonists or antagonists have shown promising results in treating TBI; however, no pragmatic clinical therapy has been found so far. The discovery of similar molecules and receptors has resulted in the expansion of the endogenous system and bred the term endocannabinoidome, which incorporates the newly discovered molecules and receptors. Ligands of the endocannabinoidome produce similar therapeutic benefits for TBI but act by different receptor pathways, which may allow one to overcome current existing problems of manipulating the endocannabinoid system for TBI treatment. Currently, therapies used to treat TBI have many unwanted side effects, establishing the need for alternative research options. This paper examines three of these endocannabinoidome molecules that have been previously researched for treating TBI and illuminates their specific receptor pathways and how these receptor pathways operate differently from the ordinary pathways of the endocannabinoid system. Gaining an understanding of the receptor pathways used by endocannabinoidome molecules will open a new field of research for therapeutics to treat TBI.
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