Document Type
Article
Publication Date
11-2020
Keywords
JMG, JAXCC
JAX Source
Aging Cell 2020 Nov; 19(11):e13269
First Page
13269
Last Page
13269
ISSN
1474-9726
PMID
33145977
DOI
https://doi.org/10.1111/acel.13269
Grant
AG022308; CA034196
Abstract
To see if variations in timing of rapamycin (Rapa), administered to middle aged mice starting at 20 months, would lead to different survival outcomes, we compared three dosing regimens. Initiation of Rapa at 42 ppm increased survival significantly in both male and female mice. Exposure to Rapa for a 3-month period led to significant longevity benefit in males only. Protocols in which each month of Rapa treatment was followed by a month without Rapa exposure were also effective in both sexes, though this approach was less effective than continuous exposure in female mice. Interpretation of these results is made more complicated by unanticipated variation in patterns of weight gain, prior to the initiation of the Rapa treatment, presumably due to the use of drug-free food from two different suppliers. The experimental design included tests of four other drugs, minocycline, β-guanidinopropionic acid, MitoQ, and 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG), but none of these led to a change in survival in either sex.
Recommended Citation
Strong R,
Miller R,
Bogue MA,
Fernandez E,
Javors M,
Libert S,
Marinez P,
Murphy M,
Musi N,
Nelson J,
Petrascheck M,
Reifsnyder PC,
Richardson A,
Salmon A,
Macchiarini F,
Harrison D.
Rapamycin-mediated mouse lifespan extension: Late-life dosage regimes with sex-specific effects. Aging Cell 2020 Nov; 19(11):e13269
Comments
This is an open access article under the terms of the Creative Commons Attribution License.