| Literature DB >> 32854519 |
Tsui-Ting Ching1, Yen-Chieh Chen1, Guang Li2,3, Jianfeng Liu3, X Z Shawn Xu2,4, Ao-Lin Hsu4,5,6,7.
Abstract
IMPACT STATEMENT: The functional decline of motor activity is a common feature in almost all aging animals that leads to frailty, loss of independence, injury, and even death in the elderly population. Thus, understanding the molecular mechanism that drives the initial stage of this functional decline and developing strategies to increase human healthspan and even lifespan by targeting this process would be of great interests to the field. In this study, we found that by precisely targeting the motor neurons to potentiate its synaptic releases either genetically or pharmacologically, we can not only delay the functional aging at NMJs but also slow the rate of aging at the organismal level. Most importantly, we have demonstrated that a critical window of time, that is the early stage of NMJs functional decline, is required for the beneficial effects. A short-term treatment within this time period is sufficient to extend the animals' lifespan.Entities:
Keywords: C. elegans; Longevity; aging; arecoline; motor neuron; neuromuscular junction; synaptic exocytosis; tomosyn
Year: 2020 PMID: 32854519 PMCID: PMC7787544 DOI: 10.1177/1535370220950639
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699