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UrduPrevious research in rats has shown that protein deficiency during pregnancy leads to lower gestational weight gain in the mother and stunted growth in male offspring. However, less is known about the effects of low dietary protein on maternal postpartum physiology and health, particularly in humans. Learning more may help “people be more cautious about what they eat during pregnancy,” wrote Yuan-Xiang Pan, PhD, corresponding author of the current study.
Pan’s research team from the University of Illinois at Urbana-Champaign studied a group of pregnant rats that were fed a low-protein diet throughout pregnancy and lactation. Compared with a control group that followed a standard diet, the low-protein group had liver enlargement as well as higher triglyceride and liver enzyme levels. These circumstances can negatively affect liver function and are risk factors associated with fatty liver disease.
The researchers found that low protein in the diet activated a protein (LC3B)—and increased expression of its associated gene—involved in a process called autophagy. Autophagy is a process in which cells digest their unnecessary or dysfunctional parts. The activation of LC3B promotes the deterioration of another protein, called APOB. APOB transports cholesterol and triglycerides in the bloodstream. This combined process ultimately caused fats (lipids) to build up in the liver, which raised triglyceride levels. In people, these phenomena can increase the risks of liver damage and non-alcoholic fatty liver disease. Learning more about the relationship between protein consumption and LC3B activation will provide insight into the genetic control of lipid accumulation in the liver.
“This finding sheds some light on understanding the molecular regulation of maternal lipid metabolism during pregnancy and lactation in response to a low-protein diet and which may help modulate maternal and prenatal health in both mother and offspring,” the researchers wrote.
Read the full article, “A low-protein diet during gestation and lactation increases hepatic lipid accumulation through autophagy and histone deacetylase,” published ahead of print in the American Journal of Physiology—Endocrinology and Metabolism.
Physiology is the study of how molecules, cells, tissues and organs function in health and disease. Established in 1887, the American Physiological Society (APS) was the first U.S. society in the biomedical sciences field. The Society represents nearly 10,000 members and publishes 15 peer-reviewed journals with a worldwide readership.
Original post https://alertarticles.info
