Scientists have developed a CPACC drug that affects the MRS2 gene, which is responsible for transporting magnesium to the mitochondria of cells. Thus, the movement of magnesium in the body slows down, which allows you to eat sweet and fatty foods and not get fat.
The experiments were performed on rats fed a high-fat, high-sugar diet regularly throughout their lives. However, the animals always remained normal weight and healthy.
The scientists explain the result by saying that sodium, calcium, magnesium and potassium are micronutrients that play an important role in maintaining a healthy metabolism. But their overdose can lead to the opposite metabolic disorders.
“While looking for factors responsible for weight gain at the cellular level in mammals, scientists noticed that energy production slows down when body cells receive more magnesium than a healthy body needs. Excess magnesium disrupts mitochondria activity in body cells, leading to excessive accumulation of fat in the body and ultimately weight gain, and liver and liver and kidney disease. leads to heart disease,” says Inc., published in the journal Cell Reports.
CPACC increased energy production in the cells of mice by suppressing MRS2 activity, allowing fat and sugar metabolism to be more efficient.
“This drug can also reduce the risk of cardiometabolic diseases such as heart attack and stroke, as well as reduce the incidence of liver cancer that can follow fatty liver disease,” said the professor of medicine, one of the study’s co-authors. At the University of Texas Health Science Center at Sun.-Antonio Madesh Muniswami.
It is important to note that CPACC has not yet been approved or patented.
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Source: Ferra
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