Plate Nº 77 · recorded September 30, 2026
Health & Medicine ResearchReported finding
Drug That Flips Cell 'Energy Saver' Switch Extends Animal Lifespans
A drug called 991 directly activated the energy sensor AMPK and extended lifespan in yeast, worms and flies by over 25% in some cases, researchers report in Aging Cell.
By Marcus Bennett4 min read789 words
In brief
- A drug called 991 directly activated AMPK and extended lifespan in yeast, worms and flies by more than 25% in some cases (Aging Cell, 2026).
- AMPK is a cellular enzyme that senses low energy — during exercise, fasting or stress — and shuts down energy-intensive processes while turning on fuel-burning ones.
- This is the first study showing that directly targeting AMPK with a drug produces longevity benefits in living organisms; mouse studies are the next step.
Scientists have prolonged the lifespan of several animal species with a drug — in some cases by more than 25%. The study, published in the journal Aging Cell, provides strong evidence that switching on a protein that governs cellular energy levels can help organisms live significantly longer.
Researchers from the MRC Laboratory of Medical Sciences (MRC LMS), Imperial College London, the University of Cologne and collaborating institutions tested the approach in fission yeast, nematode worms and fruit flies. In all three species, they observed anti-aging effects.
The cell's energy-saving switch
The target is an enzyme called AMPK, which sits inside cells and monitors energy levels in real time. When energy runs low — during exercise, fasting or stress, for example — AMPK shuts down energy-hungry processes such as building new proteins or storing fat. At the same time, it switches on energy-generating ones, like burning existing fat and sugar for fuel.
Because AMPK sits at the center of metabolic control, its disruption is linked to metabolic diseases such as type 2 diabetes and obesity. Boosting its activity, by contrast, appears to bring health benefits. Several existing medicines, including the diabetes drug metformin and weight-loss drugs like semaglutide, are known to activate AMPK. The catch is that many of these work indirectly, which makes their biological effects harder to confirm and interpret with certainty in the laboratory and the clinic.
A direct hit extends lifespan
To get around that problem, the team used a drug called 991, which targets AMPK directly. They tested it in three classic model organisms of aging research: fission yeast (S. pombe), nematode worms (C. elegans) and fruit flies (Drosophila). Researchers favor these species because they live relatively short lives, which makes experiments feasible.
Dr. Helena Cochemé, who leads the Redox Metabolism Group at MRC LMS, put the practical advantage in numbers. "The fact that we can extend lifespan in yeast, worms and flies is very exciting. Worms and flies in the lab live for around three weeks and three months, respectively, compared to roughly three years for mice, so we can make progress and discoveries much more rapidly and efficiently than in mammalian systems."
The result itself is a first, she said: "Our study is the first demonstration that directly targeting AMPK using a drug can have longevity benefits in living organisms."
Cochemé also offered a simple analogy for how the enzyme works. "AMPK is effectively the body's equivalent to the 'energy saving mode' on a mobile phone. If a treatment works successfully in three such distantly related species, then these results give us more confidence that in the longer term, the effects could translate to mammals and eventually perhaps humans."
Cleaner results, but mice come first
The direct approach has another advantage beyond efficacy. David Carling, who leads the Cellular Stress Group at MRC LMS, explained: "By switching on AMPK specifically using a direct activator, it is possible to achieve a much cleaner result, avoiding potential side effects. Now that we have very solid, convincing evidence from the laboratory model organisms, the next step will be to show that we can also improve health and extend lifespan in mice."
There is also some clinical reassurance already in hand. "Direct AMPK activators have already been used safely in clinical trials for the treatment of specific metabolic diseases," Carling noted. "This opens the door for using AMPK activators to treat a range of human diseases in the future."
Still, anyone hoping for an anti-aging pill should temper expectations. Filipe Cabreiro, who leads the Host-Microbe Co-Metabolism Group at MRC LMS and a laboratory at the University of Cologne, was blunt about the timeline: "The field is still a long way from anti-aging clinical trials in humans. This is because aging is not technically classified as a disease."
The stakes, however, are large. "But improving health in older age would be hugely beneficial from a societal and health care perspective, since aging is a major risk factor for so many diseases, such as heart disease, diabetes, cancer and dementia," Cabreiro said.
He added: "The ability to make individuals healthier for longer, for instance by pharmacologically targeting energy balance through AMPK, would be a major biomedical breakthrough."
Scientists at Queen Mary University of London, the Francis Crick Institute and the University of Lyon also contributed to the research.
What to keep in mind
The findings come from yeast, worms and flies — organisms far removed from humans. Effects in one species do not guarantee the same effects in another, and mammalian studies have not yet shown the same results. Whether the lifespan extension seen here will translate to mice, let alone people, remains an open question that only further research can answer.
via Medical Xpress (Source)
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