Burns Tammy L, Ineck Joseph R
Creighton University Medical Center, Omaha, NE 68178-4879, USA.
Ann Pharmacother. 2006 Feb;40(2):251-60. doi: 10.1345/aph.1G217. Epub 2006 Jan 31.
To review the literature concerning the physiology of the endocannabinoid system, current drug development of cannabinoid agonists, and current clinical research on the use of cannabinoid agonists for analgesia.
Articles were identified through a search of MEDLINE (1966-August 2005) using the key words cannabis, cannabinoid, cannabi*, cannabidiol, nabilone, THC, pain, and analgesia. No search limits were included. Additional references were located through review of the bibliographies of the articles identified.
Studies of cannabinoid agonists for treatment of pain were selected and were not limited by pain type or etiology. Studies or reviews using animal models of pain were also included. Articles that related to the physiology and pharmacology of the endocannabinoid system were evaluated.
The discovery of cannabinoid receptors and endogenous ligands for these receptors has led to increased drug development of cannabinoid agonists. New cannabimimetic agents have been associated with fewer systemic adverse effects than delta-9-tetrahydrocannabinol, including recent development of cannabis medicinal extracts for sublingual use (approved in Canada), and have had promising results for analgesia in initial human trials. Several synthetic cannabinoids have also been studied in humans, including 2 cannabinoid agonists available on the international market.
Cannabinoids provide a potential approach to pain management with a novel therapeutic target and mechanism. Chronic pain often requires a polypharmaceutical approach to management, and cannabinoids are a potential addition to the arsenal of treatment options.
综述有关内源性大麻素系统生理学、大麻素激动剂当前药物研发情况以及大麻素激动剂用于镇痛的当前临床研究的文献。
通过检索MEDLINE(1966年至2005年8月),使用关键词大麻、大麻素、大麻相关词、大麻二酚、纳布啡、四氢大麻酚、疼痛和镇痛来识别文章。未设置检索限制。通过查阅已识别文章的参考文献找到其他参考文献。
选择了关于大麻素激动剂治疗疼痛的研究,且不受疼痛类型或病因限制。还纳入了使用疼痛动物模型的研究或综述。对与内源性大麻素系统生理学和药理学相关的文章进行了评估。
大麻素受体及其内源性配体的发现推动了大麻素激动剂药物研发的增加。新型大麻素类似物与九氢大麻酚相比全身不良反应更少,包括近期用于舌下含服的大麻药用提取物(在加拿大获批)的研发,并且在初步人体试验中镇痛效果良好。几种合成大麻素也在人体中进行了研究,包括国际市场上可用的2种大麻素激动剂。
大麻素为疼痛管理提供了一种具有新治疗靶点和机制的潜在方法。慢性疼痛通常需要多种药物联合治疗,大麻素是治疗选择武器库中的一种潜在补充。