Pedro Amorim Neto Dionísio, Vitor Pereira de Godoy João, Tostes Katiane, Pelegrini Bosque Beatriz, Vieira Rodrigues Paulla, Aparecida Rocco Silvana, Luis Sforça Mauricio, de Castro Fonseca Matheus
Department of Food Science and Nutrition, Faculty of Food Engineering, University of Campinas, Campinas, Brazil.
Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, São Paulo, Brazil.
Neuroscience. 2023 Aug 21;526:21-34. doi: 10.1016/j.neuroscience.2023.06.010. Epub 2023 Jun 17.
Parkinson's Disease is a synucleinopathy that primarily affects the dopaminergic cells of the central nervous system, leading to motor and gastrointestinal disturbances. However, intestinal peripheral neurons undergo a similar neurodegeneration process, marked by α-synuclein (αSyn) accumulation and loss of mitochondrial homeostasis. We investigated the metabolic alterations in different biometrics that compose the gut-brain axis (blood, brain, large intestine, and feces) in an MPTP-induced mouse model of sporadic Parkinson's Disease. Animals received escalating administration of MPTP. Tissues and fecal pellets were collected, and the metabolites were identified through the untargeted Nuclear Magnetic Resonance spectroscopic (H NMR) technique. We found differences in many metabolites from all the tissues evaluated. The differential expression of metabolites in these samples mainly reflects inflammatory aspects, cytotoxicity, and mitochondrial impairment (oxidative stress and energy metabolism) in the animal model used. The direct evaluation of fecal metabolites revealed changes in several classes of metabolites. This data reinforces previous studies showing that Parkinson's disease is associated with metabolic perturbation not only in brain-related tissues, but also in periphery structures such as the gut. In addition, the evaluation of the microbiome and metabolites from gut and feces emerge as promising sources of information for understanding the evolution and progression of sporadic Parkinson's Disease.
帕金森病是一种突触核蛋白病,主要影响中枢神经系统的多巴胺能细胞,导致运动和胃肠道紊乱。然而,肠道外周神经元会经历类似的神经退行性变过程,其特征是α-突触核蛋白(αSyn)积累和线粒体稳态丧失。我们在MPTP诱导的散发性帕金森病小鼠模型中,研究了构成肠-脑轴(血液、大脑、大肠和粪便)的不同生物标志物中的代谢改变。动物接受递增剂量的MPTP给药。收集组织和粪便颗粒,并通过非靶向核磁共振光谱(1H NMR)技术鉴定代谢物。我们在所有评估的组织中发现了许多代谢物的差异。这些样本中代谢物的差异表达主要反映了所用动物模型中的炎症方面、细胞毒性和线粒体损伤(氧化应激和能量代谢)。对粪便代谢物的直接评估揭示了几类代谢物的变化。该数据强化了先前的研究,表明帕金森病不仅与脑相关组织中的代谢紊乱有关,还与肠道等外周结构中的代谢紊乱有关。此外,对肠道和粪便中的微生物群和代谢物的评估成为理解散发性帕金森病的演变和进展的有前景的信息来源。