Rapamycin increases lifespan and inhibits spontaneous tumorigenesis in inbred female mice
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Updated: May 27, 2026

The Replica Set Method: A High-throughput Approach to Quantitatively Measure Caenorhabditis elegans Lifespan
Published on: June 29, 2018
Vladimir N Anisimov1, Mark A Zabezhinski, Irina G Popovich
1Department of Carcinogenesis and Oncogerontology, N.N.Petrov Research Institute of Oncology, St. Petersburg, Russia. aging@mail.ru
Abstract:
The nutrient-sensing TOR (target of rapamycin) pathway is involved in cellular and organismal aging. Rapamycin, an inhibitor of TOR, extends lifespan in yeast, fruit flies and genetically heterogeneous mice. Here, we demonstrate that lifelong administration of rapamycin extends lifespan in female 129/Sv mice characterized by normal mean lifespan of 2 y. Importantly, rapamycin was administrated intermittently (2 weeks per month) starting from the age of 2 mo. Rapamycin inhibited age-related weight gain, decreased aging rate, increased lifespan (especially in the last survivors) and delayed spontaneous cancer. 22.9% of rapamycin-treated mice survived the age of death of the last mouse in control group. Thus we demonstrated for the first time in normal inbred mice that lifespan can be extended by rapamycin. This opens an avenue to develop optimal doses and schedules of rapamycin as an anti-aging modality.
Insights
Lifelong intermittent rapamycin administration extended lifespan in female mice. This study demonstrates rapamycin
Area of Science:
- Gerontology and Molecular Biology
- Cellular and organismal aging research
- Nutrient-sensing pathways
Background:
- The target of rapamycin (TOR) pathway regulates aging.
- Rapamycin, a TOR inhibitor, has shown lifespan extension in various model organisms.
- Lifespan extension in normal inbred mice using rapamycin has not been previously demonstrated.
Purpose of the Study:
- To investigate the effect of lifelong intermittent rapamycin administration on lifespan in female 129/Sv mice.
- To evaluate rapamycin's impact on aging rate, age-related weight gain, and cancer incidence.
- To establish rapamycin as a potential anti-aging intervention in normal inbred mice.
Main Methods:
- Lifelong intermittent administration of rapamycin (2 weeks on/2 weeks off) starting at 2 months of age.
- Monitoring lifespan, aging rate, body weight, and spontaneous cancer development in control and rapamycin-treated female 129/Sv mice.
- Statistical analysis of survival data and other health parameters.
Main Results:
- Rapamycin treatment significantly extended lifespan, particularly in the oldest mice.
- Intermittent rapamycin administration inhibited age-related weight gain and decreased the overall aging rate.
- Rapamycin delayed the onset of spontaneous cancer and increased the survival rate of the last survivors by 22.9% compared to controls.
Conclusions:
- Lifelong intermittent rapamycin administration is effective in extending lifespan in normal female inbred mice.
- Rapamycin demonstrates potential as an anti-aging therapeutic by mitigating key aging hallmarks.
- Further research into optimal rapamycin dosing and scheduling is warranted for anti-aging applications.
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