| Literature DB >> 26935741 |
Judy C Triplett1, Aaron M Swomley1, Jessime Kirk1, Kelly M Grimes2,3, Kaitilyn N Lewis2,4, Miranda E Orr2,3, Karl A Rodriguez2,3, Jian Cai5, Jon B Klein5, Rochelle Buffenstein2,3, D Allan Butterfield6,7.
Abstract
Aging is the greatest risk factor for developing neurodegenerative diseases, which are associated with diminished neurotransmission as well as neuronal structure and function. However, several traits seemingly evolved to avert or delay age-related deterioration in the brain of the longest-lived rodent, the naked mole-rat (NMR). The NMR remarkably also exhibits negligible senescence, maintaining an extended healthspan for ~75 % of its life span. Using a proteomic approach, statistically significant changes with age in expression and/or phosphorylation levels of proteins associated with neurite outgrowth and neurotransmission were identified in the brain of the NMR and include: cofilin-1; collapsin response mediator protein 2; actin depolymerizing factor; spectrin alpha chain; septin-7; syntaxin-binding protein 1; synapsin-2 isoform IIB; and dynamin 1. We hypothesize that such changes may contribute to the extended lifespan and healthspan of the NMR.Entities:
Keywords: Aging; Naked mole-rat; Neurite outgrowth; Neurotransmission; Phosphoproteomics; Proteomics
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Year: 2016 PMID: 26935741 DOI: 10.1007/s11064-016-1877-1
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996