When we get older and overweight, we develop metabolic diseases. Now we know why
Obesity and aging increase the risk of diabetes and fatty liver. Scientists have figured out what goes on inside cells and what might help stop these problems.
As we age and gain excess weight, our body's cells undergo 'stress.' This stress is marked by an overproduction of a chemical compound known as ROS (reactive oxygen species), adversely affecting the cells.
This stress elevates the risk of diabetes and leads to the conversion of the body's 'brown' fat into 'white' fat, contributing to obesity. Moreover, it increases the likelihood of accumulating excess fat in the liver. Notably, 25 percent of the Danish population has fatty liver, a prevalent cause of later liver failure and death in Western countries like Denmark.
While there is already effective and affordable medicine for diabetes, I see great potential for fatty liver, which remains one of the most significant unresolved medical problems today
In a recent study, Professor Simon Bekker-Jensen from the Department of Cellular and Molecular Medicine at the University of Copenhagen identified the factors triggering this negative progression.
"There is a protein called ZAK-alpha that 'signals' the rest of the metabolism system about the cells being stressed. This triggers a chain reaction leading to, among other things, fatty liver," he explains.
This research may pave the way for new medical interventions
Simon Bekker-Jensen and his colleagues demonstrated that by removing the ZAK-alpha protein, one can prevent aging and obesity from evolving into metabolic diseases.
This prevents the protein from 'signaling' the rest of the metabolism system. Experiments with mice and zebrafish showed promising results.
"Mice in which we deactivated the ZAK-alpha protein were much healthier than those with it. In old age, they were more active, had stronger muscles, and, importantly, did not develop various metabolic diseases," says Simon Bekker-Jensen.
Addressing scepticism about the relevance of mouse experiments to humans, he emphasizes:
"Mice are a very good model for the human metabolism system. In the laboratory, we can closely simulate the modern human lifestyle, including a lack of exercise and an unhealthy, calorie-rich diet. When mice become overweight, they develop largely the same metabolic diseases as seen in humans."
The findings from this study hold potential for new medicines that could treat and prevent metabolic diseases resulting from aging and obesity.
"While there is already effective and affordable medicine for diabetes, I see great potential for fatty liver, which remains one of the most significant unresolved medical problems today," Simon Bekker-Jensen notes and adds:
"ZAK-alpha is a well-established drug target that can be inhibited with small molecules. Therefore, we anticipate that this new knowledge will attract interest from numerous companies actively working on developing and testing drugs against metabolic diseases, including fatty liver."
The next step involves clinical studies, and there is already significant interest from various clinicians.
Read the study "ROS-induced ribosome impairment underlies ZAKα-mediated metabolic decline in obesity and aging" in Science.
Contact
Professor Simon Bekker-Jensen
sbj@sund.ku.dk
+45 20 20 49 93
Journalist og press consultant Liva Polack
liva.polack@sund.ku.dk
+45 35 32 54 64