Sharma Charu, Sadek Bassem, Goyal Sameer N, Sinha Satyesh, Kamal Mohammad Amjad, Ojha Shreesh
Department of Internal Medicine, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE.
Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE.
Evid Based Complement Alternat Med. 2015;2015:238482. doi: 10.1155/2015/238482. Epub 2015 Nov 17.
The cannabinoid molecules are derived from Cannabis sativa plant which acts on the cannabinoid receptors types 1 and 2 (CB1 and CB2) which have been explored as potential therapeutic targets for drug discovery and development. Currently, there are numerous cannabinoid based synthetic drugs used in clinical practice like the popular ones such as nabilone, dronabinol, and Δ(9)-tetrahydrocannabinol mediates its action through CB1/CB2 receptors. However, these synthetic based Cannabis derived compounds are known to exert adverse psychiatric effect and have also been exploited for drug abuse. This encourages us to find out an alternative and safe drug with the least psychiatric adverse effects. In recent years, many phytocannabinoids have been isolated from plants other than Cannabis. Several studies have shown that these phytocannabinoids show affinity, potency, selectivity, and efficacy towards cannabinoid receptors and inhibit endocannabinoid metabolizing enzymes, thus reducing hyperactivity of endocannabinoid systems. Also, these naturally derived molecules possess the least adverse effects opposed to the synthetically derived cannabinoids. Therefore, the plant based cannabinoid molecules proved to be promising and emerging therapeutic alternative. The present review provides an overview of therapeutic potential of ligands and plants modulating cannabinoid receptors that may be of interest to pharmaceutical industry in search of new and safer drug discovery and development for future therapeutics.
大麻素分子源自大麻植物,作用于1型和2型大麻素受体(CB1和CB2),这两种受体已被探索作为药物发现和开发的潜在治疗靶点。目前,临床实践中使用了许多基于大麻素的合成药物,如常见的那必隆、屈大麻酚,Δ(9)-四氢大麻酚通过CB1/CB2受体介导其作用。然而,这些基于合成大麻的化合物已知会产生不良精神效应,也被用于药物滥用。这促使我们寻找一种副作用最小的替代安全药物。近年来,许多植物大麻素已从大麻以外的植物中分离出来。多项研究表明,这些植物大麻素对大麻素受体具有亲和力、效力、选择性和功效,并能抑制内源性大麻素代谢酶,从而降低内源性大麻素系统的过度活跃。此外,与合成大麻素相比,这些天然衍生分子的副作用最小。因此,基于植物的大麻素分子被证明是一种有前景的新兴治疗选择。本综述概述了调节大麻素受体的配体和植物的治疗潜力,这可能会引起制药行业的兴趣,以便为未来治疗寻找新的、更安全的药物发现和开发。