Pérez-Morales Marcel, Espinoza-Abad Rodolfo, García-García Fabio
Health Sciences Department, Metropolitan Autonomous University, Campus Lerma, Lerma de Villada, Mexico City 52000, Estado de Mexico, Mexico.
Health Sciences Graduate Program, Health Sciences Institute, Veracruzana University, Xalapa 91190, Veracruz, Mexico.
Pharmaceuticals (Basel). 2025 Feb 18;18(2):266. doi: 10.3390/ph18020266.
Over the last three decades, the decriminalization and legalization of therapeutic and recreational marijuana consumption have increased. Consequently, the availability of marijuana-based products associated with its therapeutic use has increased. These developments have stimulated research on cannabinoids involving a wide range of animal models and clinical trials. Also, it is reported that cannabinoids promote sleep in animal models and naïve human participants, and they seem to improve insomnia and sleep apnea in patients. However, evidence from rigorous clinical trials is needed. In addition, among several physiological processes, cannabinoid receptors modulate dopamine synthesis and release. In this regard, the side effects of marijuana and marijuana derivatives must not be ignored. The chronic consumption of marijuana could reduce dopamine responsivity, increase negative emotionality, and induce anhedonia. Research on the neurobiological changes associated with cannabinoid ligands in animal models, in regard to the consumption of both marijuana and marijuana-based compounds, must improve and the effectiveness of the therapeutic outcomes in clinical trials must be guaranteed. In this review, we include a detailed description of the mechanisms of action of cannabinoids on the brain and their impact on sleep disorders and addictive behaviors to emphasize the need to understand the potential risks and benefits of their therapeutic and recreational use. Evidence from basic research and clinical trials from papers published between 2000 and 2024 are included. The pharmacodynamics of these compounds is discussed in terms of sleep-wake regulation, drug addiction, and addictive behaviors.
在过去三十年里,治疗性和娱乐性大麻消费的非刑罪化和合法化现象有所增加。因此,与大麻治疗用途相关的产品供应量也有所增加。这些发展刺激了对大麻素的研究,涉及广泛的动物模型和临床试验。此外,据报道,大麻素在动物模型和未接触过的人类参与者中可促进睡眠,而且它们似乎能改善患者的失眠和睡眠呼吸暂停。然而,仍需要来自严格临床试验的证据。此外,在多个生理过程中,大麻素受体调节多巴胺的合成和释放。在这方面,大麻及其衍生物的副作用不容忽视。长期吸食大麻可能会降低多巴胺反应性,增加负面情绪,并导致快感缺失。关于大麻和大麻基化合物的消费,在动物模型中对与大麻素配体相关的神经生物学变化的研究必须得到改进,并且必须确保临床试验中治疗效果的有效性。在本综述中,我们详细描述了大麻素对大脑的作用机制及其对睡眠障碍和成瘾行为的影响,以强调理解其治疗和娱乐用途潜在风险和益处的必要性。纳入了2000年至2024年间发表的论文中基础研究和临床试验的证据。从睡眠 - 觉醒调节、药物成瘾和成瘾行为方面讨论了这些化合物的药效学。