Seo Jung Hwa, Kang Seong-Woong, Kim Kyungri, Wi Soohyun, Lee Jang Woo, Cho Sung-Rae
Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.
Brain Korea 21 PLUS project for Medical Science, Yonsei University College of Medicine, Seoul 03722, Korea.
Antioxidants (Basel). 2020 Sep 28;9(10):928. doi: 10.3390/antiox9100928.
Although environmental enrichment (EE) is known to reduce oxidative stress in Parkinson's disease (PD), the metabolic alternations for detoxifying endogenous and xenobiotic compounds according to various brain regions are not fully elucidated yet. This study aimed to further understand the role of EE on detoxifying enzymes, especially those participating in phase I of metabolism, by investigating the levels of enzymes in various brain regions such as the olfactory bulb, brain stem, frontal cortex, and striatum. Eight-month-old transgenic PD mice with the overexpression of human A53T α-synuclein and wild-type mice were randomly allocated to either standard cage condition or EE for 2 months. At 10 months of age, the expression of detoxifying enzymes was evaluated and compared with wild-type of the same age raised in standard cages. EE improved neurobehavioral outcomes such as olfactory and motor function in PD mice. EE-treated mice showed that oxidative stress was attenuated in the olfactory bulb, brain stem, and frontal cortex. EE also reduced apoptosis and induced cell proliferation in the subventricular zone of PD mice. The overexpression of detoxifying enzymes was observed in the olfactory bulb and brain stem of PD mice, which was ameliorated by EE. These findings were not apparent in the other experimental regions. These results suggest the stage of PD pathogenesis may differ according to brain region, and that EE has a protective effect on the PD pathogenesis by decreasing oxidative stress.
尽管已知环境富集(EE)可减轻帕金森病(PD)中的氧化应激,但根据不同脑区对内源性和外源性化合物进行解毒的代谢变化尚未完全阐明。本研究旨在通过研究嗅球、脑干、额叶皮质和纹状体等不同脑区的酶水平,进一步了解EE对解毒酶的作用,尤其是那些参与代谢第一阶段的酶。将八个月大的过度表达人A53Tα-突触核蛋白的转基因PD小鼠和野生型小鼠随机分配到标准笼养条件或EE环境中饲养2个月。在10个月大时,评估解毒酶的表达,并与在标准笼中饲养的同年龄野生型小鼠进行比较。EE改善了PD小鼠的神经行为结果,如嗅觉和运动功能。接受EE治疗的小鼠显示,嗅球、脑干和额叶皮质中的氧化应激得到减轻。EE还减少了PD小鼠脑室下区的细胞凋亡并诱导了细胞增殖。在PD小鼠的嗅球和脑干中观察到解毒酶的过度表达,而EE可使其改善。这些发现在其他实验区域并不明显。这些结果表明,PD发病机制的阶段可能因脑区而异,并且EE通过降低氧化应激对PD发病机制具有保护作用。