Clinical and Experimental Neuroscience Group (NiCE-IMIB), Department of Human Anatomy and Psychobiology, Institute for Aging Research, School of Medicine, University of Murcia, Murcia, Spain.
Biomedical Research Institute of Murcia (IMIB-Arrixaca), Campus of Health Sciences, University of Murcia, Murcia, Spain.
Neurotox Res. 2019 May;35(4):918-930. doi: 10.1007/s12640-019-0010-z. Epub 2019 Feb 22.
The cause of progressive degeneration in Parkinson's disease is not clear, although, in the last years, different studies have suggested that both brain and peripheral inflammation could play a key role in the progression of this disorder. In our study, we aimed to analyze the effect of an acute inflammation confined to the colon on dopaminergic neuronal death and glial response in mice intoxicated with MPTP. The results obtained show a very significant decrease of dopaminergic neurons in the SNpc as well as a significant decrease of dopaminergic fibers in the striatum of the MPTP+DSS-treated group compared with the control animals. In addition, there was a significant exacerbation of microglial and astrocytes activation in MPTP+DSS animals compared with the control group. This data suggests that a specific gastrointestinal injury, which induces a systemic inflammatory response, is able to exacerbate cell death mechanisms of the remaining dopaminergic neurons and then contributes to the persistent progression of the disease. These results leave open new lines of research on the role of exclusive colonic inflammation and the progression of nigrostriatal dopaminergic degeneration.
帕金森病进行性退化的原因尚不清楚,尽管近年来的不同研究表明,脑和外周炎症可能在该疾病的进展中起关键作用。在我们的研究中,我们旨在分析局限于结肠的急性炎症对 MPTP 中毒小鼠中多巴胺能神经元死亡和神经胶质反应的影响。结果表明,与对照组相比,MPTP+DSS 处理组的 SNpc 中多巴胺能神经元显著减少,纹状体中的多巴胺能纤维也显著减少。此外,与对照组相比,MPTP+DSS 动物的小胶质细胞和星形胶质细胞激活明显加剧。这些数据表明,特定的胃肠道损伤会引起全身炎症反应,从而加剧剩余多巴胺能神经元的细胞死亡机制,并导致疾病的持续进展。这些结果为专门的结肠炎症和黑质纹状体多巴胺能退行性变的进展的作用开辟了新的研究途径。