Soderstrom Ken, Soliman Eman, Van Dross Rukiyah
Department of Pharmacology and Toxicology, Brody School of Medicine, East Carolina University, Greenville, NC, United States.
Department of Pharmacology and Toxicology, Zagazig University, Zagazig, Egypt.
Front Pharmacol. 2017 Oct 10;8:720. doi: 10.3389/fphar.2017.00720. eCollection 2017.
Cannabinoids include the active constituents of or are molecules that mimic the structure and/or function of these -derived molecules. Cannabinoids produce many of their cellular and organ system effects by interacting with the well-characterized CB1 and CB2 receptors. However, it has become clear that not all effects of cannabinoid drugs are attributable to their interaction with CB1 and CB2 receptors. Evidence now demonstrates that cannabinoid agents produce effects by modulating activity of the entire array of cellular macromolecules targeted by other drug classes, including: other receptor types; ion channels; transporters; enzymes, and protein- and non-protein cellular structures. This review summarizes evidence for these interactions in the CNS and in cancer, and is organized according to the cellular targets involved. The CNS represents a well-studied area and cancer is emerging in terms of understanding mechanisms by which cannabinoids modulate their activity. Considering the CNS and cancer together allow identification of non-cannabinoid receptor targets that are shared and divergent in both systems. This comparative approach allows the identified targets to be compared and contrasted, suggesting potential new areas of investigation. It also provides insight into the diverse sources of efficacy employed by this interesting class of drugs. Obtaining a comprehensive understanding of the diverse mechanisms of cannabinoid action may lead to the design and development of therapeutic agents with greater efficacy and specificity for their cellular targets.
大麻素包括大麻的活性成分,或是模拟这些源自大麻的分子的结构和/或功能的分子。大麻素通过与已被充分研究的CB1和CB2受体相互作用,产生许多细胞和器官系统效应。然而,目前已经明确,大麻素药物的并非所有效应都归因于它们与CB1和CB2受体的相互作用。现在有证据表明,大麻素类药物通过调节其他药物类别所靶向的整个细胞大分子阵列的活性来产生效应,这些大分子阵列包括:其他受体类型;离子通道;转运体;酶,以及蛋白质和非蛋白质细胞结构。本综述总结了中枢神经系统和癌症中这些相互作用的证据,并根据所涉及的细胞靶点进行组织。中枢神经系统是一个研究充分的领域,而在理解大麻素调节其活性的机制方面,癌症研究也正在兴起。将中枢神经系统和癌症放在一起考虑,可以识别出两个系统中共同和不同的非大麻素受体靶点。这种比较方法可以对已识别的靶点进行比较和对比,从而提出潜在的新研究领域。它还能深入了解这类有趣药物所采用的多种疗效来源。全面了解大麻素作用的多种机制,可能会促成针对其细胞靶点设计和开发出疗效更高、特异性更强的治疗药物。