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Rapamycin Research Shows Lifespan Effects Across Multiple Species

At a glance

  • Rapamycin extended lifespan in mice, dogs, flies, and worms in various studies
  • Effects varied by species, dosage, timing, and sex
  • Human trials reported slowed ovarian aging and improved well-being in women

Recent scientific studies have examined the impact of rapamycin on lifespan and healthspan across a range of animal models and in limited human trials. The findings indicate that the drug’s effects depend on multiple factors, including species, treatment timing, and dosage.

In mice, rapamycin administration late in life resulted in median lifespan increases of about 9% for males and 13% for females, with life expectancy at the start of treatment rising by 28% and 38% for males and females, respectively. Additional research showed that beginning treatment at nine months of age led to median survival improvements of 10% in males and 18% in females.

Short-term rapamycin exposure in middle-aged mice increased life expectancy by up to 60%, but at certain doses, it was associated with a shift in cancer prevalence toward more aggressive hematopoietic cancers in female mice. In a separate study, combining rapamycin with trametinib in mice produced a lifespan extension of around 30%, with each drug individually contributing smaller gains.

What the numbers show

  • Rapamycin increased median lifespan by 9–13% in late-life treated mice
  • Three-month treatment in mice raised life expectancy by up to 60%
  • In canine trials, lifespan rose by up to 14% with rapamycin

Research on other species has produced varied results. In fruit flies, a brief rapamycin treatment early in adulthood extended lifespan nearly as much as ongoing exposure, while starting the drug later in life had no effect. In C. elegans, mean lifespan increased by up to 21.9%, but the degree of benefit differed between trials, indicating inconsistent outcomes even under controlled conditions.

Canine studies found that low-dose rapamycin given to older dogs extended their lifespan by up to 14%. Reports from owners indicated that 27% observed health and behavior improvements, compared to 8% in a placebo group, suggesting a possible impact on quality of life as well as longevity.

Human research remains limited but includes a clinical trial in which women up to age 35 received low-dose rapamycin. The study reported a slowing of ovarian aging by about 20%, with participants also noting improvements in memory, energy, skin, and hair quality.

Across all studies, the effects of rapamycin on lifespan and healthspan have not been uniform. Outcomes have depended on variables such as species, sex, genetic background, dosage, timing of administration, and whether rapamycin was used alone or in combination with other interventions.

Overall, the research indicates that while rapamycin has shown potential to extend lifespan in several animal models and in specific human contexts, the results are influenced by a range of biological and experimental factors, leading to inconsistent findings across different studies.

* This article is based on publicly available information at the time of writing.

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