Scientists have found that altering a single gene in mice extended their average lifespan by about 20 per cent - the equivalent of raising the average human lifespan by 16 years, from 79 to 95.
Researchers at the National Institutes of Health in US lowered the expression of the gene called mTOR, which is involved in metabolism and energy balance, in mice.
The detailed study of these mice revealed that gene-influenced lifespan extension did not affect every tissue and organ the same way.
For example, the mice retained better memory and balance as they aged, but their bones deteriorated more quickly than normal.
"Rather, similar to circadian rhythms, an animal might have several organ-specific ageing clocks that generally work together to govern the ageing of the whole organism," Finkel said.
Finkel, who heads the NHLBI's Laboratory of Molecular Biology in the Division of Intramural Research, noted that these results may help guide therapies for ageing-related diseases that target specific organs, like Alzheimer's.
However, further studies in these mice as well as human cells are needed to identify exactly how ageing in these different tissues is connected at the molecular level.
The median lifespan for the mTOR mice was 28.0 months for males and 31.5 months for females, compared to 22.9 months and 26.5 months for normal males and females, respectively.
The mTOR mice also had a longer maximal lifespan; seven of the eight longest-lived mice in this study were mTOR mice. This lifespan increase is one of the largest observed in mice so far.
They generally outperformed normal mice of equivalent age in maze and balance tests, indicating better retention of memory and coordination.
Older mTOR mice also retained more muscle strength and posture. However, mTOR mice had a greater loss in bone volume as they aged, and they were more susceptible to infections at old age, suggesting a loss of immune function.
The study was published in the journal Cell Reports.
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