Motor cortex theta and gamma architecture in young adult APPswePS1dE9 Alzheimer mice
PLoS ONE, ISSN: 1932-6203, Vol: 12, Issue: 1, Page: e0169654
2017
- 11Citations
- 46Captures
- 1Mentions
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- Citations11
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- 11
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- Captures46
- Readers46
- 46
- Mentions1
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Motor Cortex Theta and Gamma Architecture in Young Adult APPswePS1dE9 Alzheimer Mice.
PLoS One. 2017;12(1):e0169654. Epub 2017 Jan 10 Authors: Papazoglou A, Soos J, Lundt A, Wormuth C, Ginde VR, Müller R, Henseler C, Broich K, Xie K, Haenisch B, Ehninger D, Weiergräber M PubMed: 28072877 Submit Comment
Article Description
Alzheimer's disease (AD) is a multifactorial disorder leading to progressive memory loss and eventually death. In this study, an APPswePS1dE9 AD mouse model has been analyzed for motor cortex theta, beta and gamma frequency alterations using computerized 3D stereotaxic electrode positioning and implantable video-EEG radiotelemetry to perform long-term M1 recordings from both genders considering age, circadian rhythm and activity status of experimental animals. We previously demonstrated that APPswePS1dE9 mice exibit complex alterations in hippocampal frequency power and another recent investigation reported a global increase of alpha, beta and gamma power in APPswePS1dE9 in females of 16±17 weeks of age. In this cortical study in APPswePS1dE9 mice we did not observe any changes in theta, beta and particularly gamma power in both genders at the age of 14, 15, 18 and 19 weeks. Importantly, no activity dependence of theta, beta and gamma activity could be detected. These findings clearly point to the fact that EEG activity, particularly gamma power exhibits developmental changes and spatial distinctiveness in the APPswePS1dE9 mouse model of Alzheimer's disease.
Bibliographic Details
10.1371/journal.pone.0169654; 10.1371/journal.pone.0169654.g001; 10.1371/journal.pone.0169654.g003; 10.1371/journal.pone.0169654.g002
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85009088533&origin=inward; http://dx.doi.org/10.1371/journal.pone.0169654; http://www.ncbi.nlm.nih.gov/pubmed/28072877; https://dx.plos.org/10.1371/journal.pone.0169654; https://dx.plos.org/10.1371/journal.pone.0169654.g001; http://dx.doi.org/10.1371/journal.pone.0169654.g001; https://dx.plos.org/10.1371/journal.pone.0169654.g003; http://dx.doi.org/10.1371/journal.pone.0169654.g003; https://dx.plos.org/10.1371/journal.pone.0169654.g002; http://dx.doi.org/10.1371/journal.pone.0169654.g002; https://dx.doi.org/10.1371/journal.pone.0169654.g003; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0169654.g003; https://dx.doi.org/10.1371/journal.pone.0169654.g002; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0169654.g002; https://dx.doi.org/10.1371/journal.pone.0169654; https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0169654; https://dx.doi.org/10.1371/journal.pone.0169654.g001; https://journals.plos.org/plosone/article/figure?id=10.1371/journal.pone.0169654.g001; http://www.plosone.org/article/metrics/info:doi/10.1371/journal.pone.0169654; http://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0169654&type=printable; http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0169654; https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0169654&type=printable; http://dx.plos.org/10.1371/journal.pone.0169654.g001; http://dx.plos.org/10.1371/journal.pone.0169654.g002; http://dx.plos.org/10.1371/journal.pone.0169654; http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0169654; http://dx.plos.org/10.1371/journal.pone.0169654.g003
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