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Enhancement of mitochondrial function correlates with the extension of lifespan by caloric restriction and caloric restriction mimetics in yeast

Authors
Choi, Kyung-MiLee, Hye-LanKwon, Young-YonKang, Mi-SunLee, Sung-KeunLee, Cheol-Koo
Issue Date
8-Nov-2013
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Caloric restriction; Caloric restriction mimetics; Rapamycin; Reactive oxygen species; Mitochondrial membrane potential; ATP
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.441, no.1, pp.236 - 242
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
441
Number
1
Start Page
236
End Page
242
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/101622
DOI
10.1016/j.bbrc.2013.10.049
ISSN
0006-291X
Abstract
Caloric restriction mimetics (CRMs) have been developed to mimic the effects of caloric restriction (CR). However, research reports for the effects of CRMs are often times inconsistent across different research groups. Therefore, in this study, we compared seven identified CRMs which extend the lifespans of various organisms including caffeine, curcumin, dapsone, metformin, rapamycin, resveratrol, and spermidine to CR for mitochondrial function in a single model, Saccharomyces cerevisiae. In this organism, rapamycin extended chronological lifespan (CLS), but other CRMs failed to extend CLS. Rapamycin enhanced mitochondrial function like CR did, but other CRMs did not. Both CR and rapamycin worked on mitochondrial function, but they worked at different windows of time during the chronological aging process. (C) 2013 Elsevier Inc. All rights reserved.
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