Researchers may have found a way to turn back time and restore the liver, reversing damage from stress and aging.
While the liver is one of the body’s most resilient organs, it is still vulnerable to the ravages of stress and aging, leading to disease, severe scarring, and failure.
In experiments using mice and liver tissue from humans, the researchers identified how the aging process prompts certain liver cells to die off. They were then able to reverse the process in the animals with an investigational drug.
The finding, which appears in the journal Nature Aging, holds promise for the millions of people who have some degree of liver damage—livers that are essentially old due to the metabolic stresses of high cholesterol, obesity, diabetes, or other factors.
“Our study demonstrates that aging is at least partially reversible,” says senior author Anna Mae Diehl, professor of medicine at the Duke University School of Medicine. “You are never too old to get better.”
Diehl and colleagues set out to understand how non-alcoholic liver disease develops into a severe condition called cirrhosis, in which scarring can lead to organ failure. Aging is a key risk factor for cirrhosis among those who have been diagnosed with non-alcoholic liver disease, known as metabolic dysfunction-associated steatotic liver disease, or MASLD. One in three adults worldwide have the disease.
“It’s like we had old mice eating hamburgers and fries, and we made their livers like those of young teenagers eating hamburgers and fries.”
Studying the livers of mice, the researchers identified a genetic signature distinct to old livers. Compared to young livers, the old organs had an abundance of genes that were activated to cause degeneration of hepatocytes, the main functioning cells of the liver.
“We found that aging promotes a type of programmed cell death in hepatocytes called ferroptosis, which is dependent on iron,” Diehl says. “Metabolic stressors amplify this death program, increasing liver damage.”
Armed with their genetic signature of old livers, the researchers analyzed human liver tissue and found that the livers of people diagnosed with obesity and MASLD carried the signature, and the worse their disease, the stronger the signal.
Importantly, key genes in the livers of people with MASLD were highly activated to promote cell death through ferroptosis. This gave the researchers a definitive target.
“There are things we can use to block that,” Diehl says.
Again turning to mice, the researchers fed young and old mice diets that caused them to develop MASLD. They then gave half the animals a placebo drug and the other half a drug called Ferrostatin-1, which inhibits the cell death pathway.
Upon analysis after treatment, the livers of the animals given Ferrostatin-1 looked biologically like young, healthy livers—even in the old animals that were kept on the disease-inducing diet.
“This is hopeful for all of us,” Diehl says. “It’s like we had old mice eating hamburgers and fries, and we made their livers like those of young teenagers eating hamburgers and fries.”
Diehl says the team also looked at how the ferroptosis process in the liver affects the function of other organs, which are often damaged as MASLD progresses. The genetic signature was able to differentiate between diseased and healthy hearts, kidneys, and pancreases, indicating that damaged livers amplify ferroptotic stress in other tissues.
“Together, we’ve shown that aging exacerbates non-alcoholic liver disease by creating ferroptic stress, and by reducing this impact, we can reverse the damage,” Diehl says.
The National Institutes of Health, Boehringer Ingelheim Pharmaceuticals, Inc., and the 021 AASLD Pinnacle Award supported the work.
Source: Duke University
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