Cannabinoids And Cannabinoid-Like Compounds: Biochemical Characterization And Pharmacological Perspectives

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL
O. Kytikova, Y. Denisenko, T. Novgorodtseva, I. S. Kovalenko
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引用次数: 0

Abstract

Publication interest in cannabinoids, including phytocannabinoids, endogenous cannabinoids, synthetic cannabinoids and cannabinomimetic compounds, is due to the therapeutic potential of these compounds in inflammatory pathology. Since recent years, scientific interest was focused on compounds with cannabinomimetic activity. The therapeutic use of phytocannabinoids and endocannabinoids is somewhat limited due to unresolved issues of dosing, toxicity and safety in humans, while cannabinoid-like compounds combine similar therapeutic effects with a high confirmed safety. Targets for endocannabinoids and phytocannabinoids are endocannabinoid receptors 1 and 2, G protein-coupled receptors (GPCRs), peroxisome proliferator-activated receptors (PPARs), and transient receptor potential ion channels (TRPs). Non-endocannabinoid N-acylethanolamines do not interact with cannabinoid receptors and exhibit agonist activity towards non-cannabinoid receptors, such as PPARs, GPCRs and TRPs. This literature review includes contemporary information on the biological activity, metabolism and pharmacological properties of cannabinoids and cannabinoid-like compounds, as well as their receptors. We established that only a few studies were devoted to the relationship of non-endocannabinoid N-acylethanolamines with non-cannabinoid receptors, such as PPARs, GPCRs, and also with TRPs. We have focused on issues that were insufficiently covered in the published sources in order to identify gaps in existing knowledge and determine the prospects for scientific research.
大麻素和大麻素样化合物:生化表征和药理学观点
对大麻素(包括植物大麻素、内源性大麻素、合成大麻素和拟大麻素化合物)的出版兴趣是由于这些化合物在炎症病理学中的治疗潜力。近年来,科学兴趣集中在具有大麻素活性的化合物上。由于未解决的人体剂量、毒性和安全性问题,植物大麻素和内源性大麻素的治疗用途在一定程度上受到限制,而大麻素样化合物具有类似的治疗效果和高度确认的安全性。内源性大麻素和植物大麻素的作用靶点包括内源性大麻素受体1和2、G蛋白偶联受体(gpcr)、过氧化物酶体增殖物激活受体(ppar)和瞬时受体电位离子通道(TRPs)。非内源性大麻素n-酰基乙醇胺不与大麻素受体相互作用,并对非大麻素受体(如ppar、gpcr和TRPs)表现出激动剂活性。这篇文献综述包括大麻素和大麻素样化合物及其受体的生物活性、代谢和药理学特性的当代信息。我们确定,只有少数研究致力于非内源性大麻素n-酰基乙醇胺与非大麻素受体(如ppar, gpcr)以及TRPs的关系。我们把重点放在已发表的来源中没有充分涵盖的问题上,以便确定现有知识中的差距并确定科学研究的前景。
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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来源期刊
Russian Open Medical Journal
Russian Open Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
0.90
自引率
0.00%
发文量
39
期刊介绍: Russian Open Medical Journal (RusOMJ) (ISSN 2304-3415) is an international peer reviewed open access e-journal. The website is updated quarterly with the RusOMJ’s latest original research, clinical studies, case reports, reviews, news, and comment articles. This Journal devoted to all field of medicine. All the RusOMJ’s articles are published in full on www.romj.org with open access and no limits on word counts. Our mission is to lead the debate on health and to engage, inform, and stimulate doctors, researchers, and other health professionals in ways that will improve outcomes for patients. The RusOMJ team is based mainly in Saratov (Russia), although we also have editors elsewhere in Russian and in other countries.
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