AI Article Synopsis

  • Multiple system atrophy (MSA) is a neurodegenerative disorder marked by symptoms similar to Parkinson's, as well as sleep disturbances, yet the effects on sleep in the PLP α-SYN mouse model, which closely resembles MSA, haven’t been studied.
  • Our research found notable changes in the EEG patterns of the PLP α-SYN model that align with findings from clinical studies, as well as age-dependent muscle activity during REM sleep, suggesting the model's validity for studying MSA.
  • We advocate for further investigation into our findings for their predictive validity in future studies and highlight the need for effective treatments, with our study possibly providing key biomarkers for drug development in MSA.

Article Abstract

Multiple system atrophy (MSA) is a neurodegenerative movement disorder characterized by parkinsonian symptoms and cerebellar symptoms. Sleep disturbances also play a crucial role in MSA. One of the most convincing animal models in MSA research is the PLP α-SYN model, but to date no studies on sleep disturbances in this mouse model, frequently found in MSA patients are available. We identified spectral shifts within the EEG of the model, strikingly resembling results of clinical studies. We also characterized muscle activity during REM sleep, which is one of the key symptoms in REM sleep behavioral disorder. Spectral shifts and REM sleep-linked muscle activity were age dependent, supporting Face Validity of the PLP α-SYN model. We also strongly suggest our findings to be critically evaluated for Predictive Validity in future studies. Currently, research on MSA lacks potential compounds attenuating or curing MSA. Future drugs must prove its potential in animal models, for this our study provides potential biomarkers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222844PMC
http://dx.doi.org/10.3389/fnbeh.2016.00252DOI Listing

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