Parkinson Disorders Research Program, Iowa Center for Advanced Neurotoxicology, Department of Biomedical Sciences, Iowa State University (ISU), Ames, IA, 50011, USA.
Department of Statistics, Iowa State University, Ames, IA, USA.
Neurotoxicology. 2019 Dec;75:186-199. doi: 10.1016/j.neuro.2019.09.004. Epub 2019 Sep 7.
Gastrointestinal (GI) disturbances are one of the earliest symptoms affecting most patients with Parkinson's disease (PD). In many cases, these symptoms are observed years before motor impairments become apparent. Hence, the molecular and cellular underpinnings that contribute to this early GI dysfunction in PD have actively been explored using a relevant animal model. The MitoPark model is a chronic, progressive mouse model recapitulating several key pathophysiological aspects of PD. However, GI dysfunction and gut microbiome changes have not been categorized in this model. Herein, we show that decreased GI motility was one of the first non-motor symptoms to develop, evident as early as 8 weeks with significantly different transit times from 12 weeks onwards. These symptoms were observed well before motor symptoms developed, thereby paralleling PD progression in humans. At age 24 weeks, we observed increased colon transit time and reduced fecal water content, indicative of constipation. Intestinal inflammation was evidenced with increased expression of iNOS and TNFα in the small and large intestine. Specifically, iNOS was observed mainly in the enteric plexi, indicating enteric glial cell activation. A pronounced loss of tyrosine hydroxylase-positive neurons occurred at 24 weeks both in the mid-brain region as well as the gut, leading to a corresponding decrease in dopamine (DA) production. We also observed decreased DARPP-32 expression in the colon, validating the loss of DAergic neurons in the gut. However, the total number of enteric neurons did not significantly differ between the two groups. Metabolomic gas chromatography-mass spectrometry analysis of fecal samples showed increased sterol, glycerol, and tocopherol production in MitoPark mice compared to age-matched littermate controls at 20 weeks of age while 16 s microbiome sequencing showed a transient temporal increase in the genus Prevotella. Altogether, the data shed more light on the role of the gut dopaminergic system in maintaining intestinal health. Importantly, this model recapitulates the chronology and development of GI dysfunction along with other non-motor symptoms and can become an attractive translational animal model for pre-clinical assessment of the efficacy of new anti-Parkinsonian drugs that can alleviate GI dysfunction in PD.
胃肠道(GI)紊乱是影响大多数帕金森病(PD)患者的最早症状之一。在许多情况下,这些症状在运动障碍变得明显之前数年就已经出现。因此,使用相关的动物模型积极探索了导致 PD 早期胃肠道功能障碍的分子和细胞基础。MitoPark 模型是一种慢性、进行性的小鼠模型,可再现 PD 的几个关键病理生理方面。然而,该模型并未对胃肠道功能障碍和肠道微生物组变化进行分类。本文中,我们发现,胃肠道蠕动减少是最早出现的非运动症状之一,早在 8 周时就已经明显,并且从 12 周开始,其通过时间明显不同。这些症状在运动症状出现之前就已经出现,从而与人类 PD 的进展相平行。在 24 周时,我们观察到结肠通过时间增加,粪便含水量减少,表明存在便秘。小肠和大肠中 iNOS 和 TNFα表达增加表明存在肠道炎症。具体而言,iNOS 主要存在于肠丛中,表明肠胶质细胞活化。在 24 周时,中脑区域和肠道中均观察到酪氨酸羟化酶阳性神经元的明显丢失,导致多巴胺(DA)产生相应减少。我们还观察到结肠中 DARPP-32 表达减少,证实了肠道中 DA 能神经元的丢失。然而,两组之间的肠神经元总数没有显著差异。粪便样品的代谢组气相色谱-质谱分析显示,与年龄匹配的同窝对照相比,MitoPark 小鼠在 20 周时粪便中固醇、甘油和生育酚的产生增加,而 16s 微生物组测序显示普雷沃氏菌属的数量暂时增加。总的来说,这些数据进一步阐明了肠道多巴胺能系统在维持肠道健康中的作用。重要的是,该模型再现了 GI 功能障碍以及其他非运动症状的发生时间和发展过程,可成为评估新的抗帕金森药物疗效的有吸引力的转化动物模型,这些药物可以缓解 PD 中的胃肠道功能障碍。