合成和天然FAAH抑制剂的社会心理和生物学方面

David A Dawson
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引用次数: 2

摘要

分子工程师正在研究FAAH作为药物的靶点,因为控制FAAH的水平可能会产生一些同样的健康影响,这让临床医生对植物大麻素药物的潜力感到兴奋。合成大麻素通过向系统中注入与四氢大麻酚和其他植物大麻素结构相似的分子来起作用。理论上,抑制身体产生FAAH的药物通过最大化神经系统中缺乏的内源性大麻素的浓度来产生类似的效果。技术限制加上许多主要研究型大学对生物大麻素研究的抑制,限制了我们对内源性大麻素系统的理解。为了提供生物FAAH抑制剂与合成FAAH抑制剂的全面比较,仍然需要回答一些问题。旨在了解内源性和外源性大麻素的进展和研究,特别是反式-Δ -四氢大麻酚(THC)分子及其内源性大麻素等同物anandamide的药用特性,受到美国食品和药物管理局(FDA)、美国缉毒局(DEA)、美国国立卫生研究院(NIH)和美国国家药物滥用研究所(NIDA)的限制性限制。这些实体的使命宣言有效地整合在一起,以确保四氢大麻酚药用特性的研究和利用几乎不可能实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Psychosocial and Biological Aspects of Synthetic and Natural FAAH Inhibitors
Molecular engineers are studying FAAH as a target for pharmaceuticals as controlling levels of FAAH may produce some of the same health effects that excite clinicians about the potential for phytocannabinoid-based medicines. Synthetic cannabinoids work by flooding the system with molecules structurally similar to THC and other phytocannabinoids. Medicines that inhibit the body’s production of FAAH are theorized to have a similar effect by maximizing the concentration of deficient endocannabinoids in the nervous system. Technological limitations coupled with a suppression of research of biologic cannabinoids at many major research universities have limited our understanding of the endocannabinoid system. Questions still need to be answered to provide a comprehensive comparison of biologic with synthetic FAAH inhibitors. Advancement and research aimed at understanding of endogenous and exogenous cannabinoids, and particularly the medicinal properties of the Trans-Δ⁹-Tetrahydrocannabinol (THC) molecule and its endocannabinoid equivalent anandamide are hindered by prohibitive restrictions resulting from the Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), National Institute of Health (NIH), and the National Institute on Drug Abuse (NIDA). The mission statements of each of these entities effectively integrate to ensure research and utilization of the medicinal properties of THC will be nearly impossible to attain.
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