More Sandeep Vasant, Choi Dong-Kug
Department of Biotechnology, College of Biomedical and Health Science, Konkuk University, Chungju, 380-701, South Korea.
Mol Neurodegener. 2015 Apr 8;10:17. doi: 10.1186/s13024-015-0012-0.
Parkinson's disease (PD) is a slow insidious neurological disorder characterized by a loss of dopaminergic neurons in the midbrain. Although several recent preclinical advances have proposed to treat PD, there is hardly any clinically proved new therapeutic for its cure. Increasing evidence suggests a prominent modulatory function of the cannabinoid signaling system in the basal ganglia. Hence, use of cannabinoids as a new therapeutic target has been recommended as a promising therapy for PD. The elements of the endocannabinoid system are highly expressed in the neural circuit of basal ganglia wherein they bidirectionally interact with dopaminergic, glutamatergic, and GABAergic signaling systems. As the cannabinoid signaling system undergoes a biphasic pattern of change during progression of PD, it explains the motor inhibition typically observed in patients with PD. Cannabinoid agonists such as WIN-55,212-2 have been demonstrated experimentally as neuroprotective agents in PD, with respect to their ability to suppress excitotoxicity, glial activation, and oxidative injury that causes degeneration of dopaminergic neurons. Additional benefits provided by cannabinoid related compounds including CE-178253, oleoylethanolamide, nabilone and HU-210 have been reported to possess efficacy against bradykinesia and levodopa-induced dyskinesia in PD. Despite promising preclinical studies for PD, use of cannabinoids has not been studied extensively at the clinical level. In this review, we reassess the existing evidence suggesting involvement of the endocannabinoid system in the cause, symptomatology, and treatment of PD. We will try to identify future threads of research that will help in the understanding of the potential therapeutic benefits of the cannabinoid system for treating PD.
帕金森病(PD)是一种隐匿性进展的神经系统疾病,其特征是中脑多巴胺能神经元缺失。尽管最近在临床前研究方面取得了一些进展,提出了治疗PD的方法,但几乎没有经过临床验证的新疗法可治愈该病。越来越多的证据表明,大麻素信号系统在基底神经节中具有重要的调节功能。因此,将大麻素作为新的治疗靶点已被推荐为一种有前景的PD治疗方法。内源性大麻素系统的成分在基底神经节的神经回路中高度表达,在那里它们与多巴胺能、谷氨酸能和γ-氨基丁酸能信号系统进行双向相互作用。由于大麻素信号系统在PD进展过程中呈现双相变化模式,这解释了PD患者中常见的运动抑制现象。实验证明,大麻素激动剂如WIN-55,212-2在PD中具有神经保护作用,因为它们能够抑制导致多巴胺能神经元变性的兴奋性毒性、胶质细胞活化和氧化损伤。据报道,包括CE-178253、油酰乙醇胺、纳布啡和HU-210在内的大麻素相关化合物还具有对抗PD患者运动迟缓及左旋多巴诱导的运动障碍的功效。尽管针对PD的临床前研究前景乐观,但大麻素在临床层面的应用尚未得到广泛研究。在这篇综述中我们重新评估了现有证据,这些证据表明内源性大麻素系统与PD的病因、症状及治疗有关。我们将尝试确定未来的研究方向,这将有助于理解大麻素系统对治疗PD的潜在治疗益处。