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Potential Prion Involvement in Long COVID-19 Neuropathology, Including Behavior
GB. Stefano, P. Büttiker, S. Weissenberger, M. Anders, J. Raboch, R. Ptacek, RM. Kream
Language English Country United States
Document type Journal Article, Review
NLK
Medline Complete (EBSCOhost)
from 2007-02-01 to 1 year ago
Springer Nature OA/Free Journals
from 1981-03-01
- MeSH
- COVID-19 * MeSH
- Humans MeSH
- Post-Acute COVID-19 Syndrome MeSH
- Prions * metabolism MeSH
- Reactive Oxygen Species MeSH
- SARS-CoV-2 MeSH
- Mammals metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Prion' is a term used to describe a protein infectious particle responsible for several neurodegenerative diseases in mammals, e.g., Creutzfeldt-Jakob disease. The novelty is that it is protein based infectious agent not involving a nucleic acid genome as found in viruses and bacteria. Prion disorders exhibit, in part, incubation periods, neuronal loss, and induce abnormal folding of specific normal cellular proteins due to enhancing reactive oxygen species associated with mitochondria energy metabolism. These agents may also induce memory, personality and movement abnormalities as well as depression, confusion and disorientation. Interestingly, some of these behavioral changes also occur in COVID-19 and mechanistically include mitochondrial damage caused by SARS-CoV-2 and subsequenct production of reactive oxygen species. Taken together, we surmise, in part, long COVID may involve the induction of spontaneous prion emergence, especially in individuals susceptible to its origin may thus explain some of its manesfestions post-acute viral infection.
References provided by Crossref.org
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