Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran.
Phytomedicine. 2023 Jun;114:154771. doi: 10.1016/j.phymed.2023.154771. Epub 2023 Mar 15.
Cannabidiol (CBD) is one of the main phytocannabinoids found in Cannabis sativa. In contrast to Δ9-tetrahydrocannabinol, it has a low affinity for cannabinoid receptors CB1 and CB2, thereby it does not induce significant psychoactive effects. However, CBD may interact with other receptors, including peroxisome proliferator-activated receptor gamma (PPARγ). CBD is a PPARγ agonist and changes its expression. There is considerable evidence that CBD's effects are mediated by its interaction with PPARγ. So, we reviewed studies related to the interaction of CBD and PPARγ.
In this comprehensive literature review, the term 'cannabidiol' was used in combination with the following keywords including 'PPARγ', 'Alzheimer's disease', 'Parkinson's disease', 'seizure', 'multiple sclerosis', 'immune system', 'cardiovascular system', 'cancer', and 'adipogenesis'. PubMed, Web of Science, and Google Scholar were searched until December 20, 2022. A total of 78 articles were used for the reviewing process.
CBD, via activation of PPARγ, promotes significant pharmacological effects. The present review shows that the effects of CBD on Alzheimer's disease and memory, Parkinson's disease and movement disorders, multiple sclerosis, anxiety and depression, cardiovascular system, immune system, cancer, and adipogenesis are mediated, at least in part, via PPARγ.
CBD not only activates PPARγ but also affects its expression in the body. It was suggested that the late effects of CBD are mediated via PPARγ activation. We suggested that CBD's chemical structure is a good backbone for developing new dual agonists. Combining it with other chemicals enhances their biological effectiveness while reducing their dosage. The present study indicated that PPARγ is a key target for CBD, and its activation by CBD should be considered in all future studies.
大麻二酚(CBD)是大麻中发现的主要植物大麻素之一。与 Δ9-四氢大麻酚不同,它对大麻素受体 CB1 和 CB2 的亲和力较低,因此不会引起明显的精神活性作用。然而,CBD 可能与其他受体相互作用,包括过氧化物酶体增殖物激活受体 γ(PPARγ)。CBD 是 PPARγ 的激动剂,并改变其表达。有大量证据表明,CBD 的作用是通过其与 PPARγ 的相互作用介导的。因此,我们综述了与 CBD 和 PPARγ 相互作用相关的研究。
在本次全面的文献综述中,使用了“大麻二酚”一词,并与以下关键词组合使用,包括“PPARγ”、“阿尔茨海默病”、“帕金森病”、“癫痫发作”、“多发性硬化症”、“免疫系统”、“心血管系统”、“癌症”和“脂肪生成”。检索了 PubMed、Web of Science 和 Google Scholar,截至 2022 年 12 月 20 日,共使用了 78 篇文章进行综述。
CBD 通过激活 PPARγ 发挥显著的药理作用。本综述表明,CBD 对阿尔茨海默病和记忆、帕金森病和运动障碍、多发性硬化症、焦虑和抑郁、心血管系统、免疫系统、癌症和脂肪生成的影响至少部分是通过 PPARγ 介导的。
CBD 不仅激活 PPARγ,还影响其在体内的表达。有研究表明,CBD 的后期作用是通过 PPARγ 激活介导的。我们认为 CBD 的化学结构是开发新型双重激动剂的良好骨架。将其与其他化学物质结合可以提高它们的生物有效性,同时降低剂量。本研究表明,PPARγ 是 CBD 的关键靶点,在未来所有研究中都应考虑 CBD 对其的激活作用。