| Literature DB >> 29713806 |
Manish Chamoli1, Shankar J Chinta1,2, Julie K Andersen3.
Abstract
Several studies have suggested that increases in astrocytic monoamine oxidase B (MAO-B) levels in conjunction with Parkinson's disease (PD) may contribute to subsequent neuropathology associated with the disorder. MAO-B inhibitors are currently widely used as symptomatic therapeutics for PD and, although somewhat controversial, these drugs may also exhibit disease-modifying properties. To obtain a better understanding of the potential role of MAO-B in disease neuropathology, we created an inducible astrocyte-specific transgenic MAO-B mouse model. Here, we summarize findings associated with this model, including neuropathological PD features associated with it.Entities:
Keywords: Brain aging; Cellular senescence; MAO-B; Mitochondrial dysfunction; Neuroinflammation; Oxidative stress; Parkinson disease; Transgenic
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Year: 2018 PMID: 29713806 DOI: 10.1007/s00702-018-1887-z
Source DB: PubMed Journal: J Neural Transm (Vienna) ISSN: 0300-9564 Impact factor: 3.575