Kim Hyo Geun, Park Gunhyuk, Piao Ying, Kang Min Seo, Pak Youngmi Kim, Hong Seon-Pyo, Oh Myung Sook
Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University, #1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Department of Life and Nanopharmaceutical Sciences and Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University, #1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Food Chem Toxicol. 2014 Mar;65:293-300. doi: 10.1016/j.fct.2013.12.037. Epub 2014 Jan 2.
Parkinson's disease (PD) is generally characterized by the progressive loss of dopaminergic neurons projecting from the substantia nigra pars compacta (SNpc) to the striatum that results in movement dysfunction, but also entails mitochondrial dysfunction. The purpose of this study is to evaluate the protective effects of Moutan Cortex Radicis (MCE, Moutan peony) on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced PD-like symptoms and to elucidate the underlying mechanisms of action, with a focus on mitochondrial function. In a rat primary mesencephalic culture system, MCE significantly protected dopaminergic neurons from the neurotoxic effects of 1-methyl-4-phenylpyridinium (MPP(+)), an active form of MPTP. Additionally, in a subacute mouse model of MPTP-induced PD, MCE resulted in enhanced recovery from PD-like motor symptoms, including increased locomotor activity and reduced bradykinesia. MCE increased dopamine availability and protected against MPTP-induced dopaminergic neuronal damage. Moreover, MCE inhibited MPTP-induced mitochondrial dysfunction and resulted in increased expression of phosphorylated Akt, ND9, mitochondrial transcription factor A, and H2AX in the SNpc. Mitochondria-mediated apoptosis was also inhibited, via the regulation of B-cell lymphoma family proteins and the inhibition of cytochrome C release and caspase-3 activation. These results indicate that MCE has neuroprotective effects in PD models and may be useful for preventing or treating PD.
帕金森病(PD)的一般特征是,从中脑黑质致密部(SNpc)投射到纹状体的多巴胺能神经元进行性丧失,这会导致运动功能障碍,同时还伴有线粒体功能障碍。本研究的目的是评估牡丹皮(MCE,牡丹)对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病样症状的保护作用,并阐明其潜在的作用机制,重点是线粒体功能。在大鼠原代中脑培养系统中,MCE显著保护多巴胺能神经元免受MPTP的活性形式1-甲基-4-苯基吡啶离子(MPP(+))的神经毒性作用。此外,在MPTP诱导的帕金森病亚急性小鼠模型中,MCE使帕金森病样运动症状的恢复增强,包括运动活性增加和运动迟缓减轻。MCE增加了多巴胺的可用性,并防止了MPTP诱导的多巴胺能神经元损伤。此外,MCE抑制了MPTP诱导的线粒体功能障碍,并导致SNpc中磷酸化Akt、ND9、线粒体转录因子A和H2AX的表达增加。线粒体介导的细胞凋亡也通过调节B细胞淋巴瘤家族蛋白以及抑制细胞色素C释放和半胱天冬酶-3激活而受到抑制。这些结果表明,MCE在帕金森病模型中具有神经保护作用,可能对预防或治疗帕金森病有用。