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大麻药理学:常见因素与一些有前景的线索

Cannabis Pharmacology: The Usual Suspects and a Few Promising Leads.

作者信息

Russo Ethan B, Marcu Jahan

机构信息

PHYTECS, Los Angeles, CA, United States.

Americans for Safe Access, Patient Focused Certification, Washington, DC, United States.

出版信息

Adv Pharmacol. 2017;80:67-134. doi: 10.1016/bs.apha.2017.03.004. Epub 2017 Jun 5.

Abstract

The golden age of cannabis pharmacology began in the 1960s as Raphael Mechoulam and his colleagues in Israel isolated and synthesized cannabidiol, tetrahydrocannabinol, and other phytocannabinoids. Initially, THC garnered most research interest with sporadic attention to cannabidiol, which has only rekindled in the last 15 years through a demonstration of its remarkably versatile pharmacology and synergy with THC. Gradually a cognizance of the potential of other phytocannabinoids has developed. Contemporaneous assessment of cannabis pharmacology must be even far more inclusive. Medical and recreational consumers alike have long believed in unique attributes of certain cannabis chemovars despite their similarity in cannabinoid profiles. This has focused additional research on the pharmacological contributions of mono- and sesquiterpenoids to the effects of cannabis flower preparations. Investigation reveals these aromatic compounds to contribute modulatory and therapeutic roles in the cannabis entourage far beyond expectations considering their modest concentrations in the plant. Synergistic relationships of the terpenoids to cannabinoids will be highlighted and include many complementary roles to boost therapeutic efficacy in treatment of pain, psychiatric disorders, cancer, and numerous other areas. Additional parts of the cannabis plant provide a wide and distinct variety of other compounds of pharmacological interest, including the triterpenoid friedelin from the roots, canniprene from the fan leaves, cannabisin from seed coats, and cannflavin A from seed sprouts. This chapter will explore the unique attributes of these agents and demonstrate how cannabis may yet fulfil its potential as Mechoulam's professed "pharmacological treasure trove."

摘要

大麻药理学的黄金时代始于20世纪60年代,当时以色列的拉斐尔·梅舒拉姆及其同事分离并合成了大麻二酚、四氢大麻酚和其他植物大麻素。最初,四氢大麻酚吸引了大部分研究兴趣,大麻二酚只是偶尔受到关注,直到最近15年,其卓越的多功能药理学特性以及与四氢大麻酚的协同作用才重新引发了人们的兴趣。渐渐地,人们对其他植物大麻素的潜力有了认识。对大麻药理学的当代评估必须更加全面。长期以来,医疗和娱乐消费者都认为某些大麻化学变种具有独特属性,尽管它们在大麻素谱方面相似。这使得人们进一步研究单萜和倍半萜对大麻花制剂效果的药理学贡献。研究表明,这些芳香化合物在大麻整体成分中发挥的调节和治疗作用远超基于其在植物中适度含量的预期。萜类化合物与大麻素之间的协同关系将得到突出展示,其中包括许多互补作用,可提高在疼痛、精神疾病、癌症及许多其他领域的治疗效果。大麻植物的其他部分还含有多种具有药理学意义的独特化合物,包括来自根部的三萜类化合物软木三萜酮、来自扇形叶的大麻戊烯、来自种皮的大麻素以及来自种子芽的大麻黄素A。本章将探讨这些物质的独特属性,并展示大麻如何有可能实现其作为梅舒拉姆所称的“药理学宝库”的潜力。

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