This protein in liver could prevent stiff arteries in obesity and diabetes

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In a study from the University of Missouri, scientists found the importance of the protein adropin in preventing stiffness in the arteries of people with obesity and type 2 diabetes.

Arterial stiffness is a condition associated with aging and insulin resistance, a chronic condition associated with obesity.

It is a major contributor to the development of cardiovascular disease, including heart attack and stroke.

Adropin, a protein produced by the liver and other tissues, is involved in maintaining energy balance in the body and the metabolism of fat and sugar.

Previous studies have suggested that adropin also plays a role in regulating cardiovascular health.

People with chronic conditions such as obesity and type 2 diabetes have been found to have lower levels of adropin in the bloodstream.

In the study, researchers reported decreased expression of adropin in the liver was associated with both an elevated body mass index and hemoglobin A1c, a marker of glycemic control, in patients undergoing bariatric surgery.

In a separate group, people with type 2 diabetes had lower adropin levels and increased arterial stiffness when compared to healthy controls.

In addition, they studied arteries isolated from mice that were lacking adropin. They reported that “loss of adropin alone causes an increase in arterial stiffness, mimicking the effects of obesity and type 2 diabetes.”

The researchers later used adropin to treat arterial stiffening in a mouse model of obesity and type 2 diabetes and found that adropin exposure reduces obesity and type 2 diabetes-associated arterial stiffening.

These findings suggest that people with low adropin levels are more likely to develop arterial stiffening.

Therefore, greater consideration should be given to adropin as a potential target in the prevention and treatment of heart disease in people with obesity and type 2 diabetes.

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The study was conducted by Thomas J. Jurrissen et al and published in the American Journal of Physiology-Heart and Circulatory Physiology.

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