Public Release: 23-Feb-2016
Natural sugar may treat fatty liver disease
Mouse study shows the sugar trehalose triggers liver cells to clean up their excess fat
Washington University School of Medicine
Nonalcoholic fatty liver disease, a condition closely linked to obesity, affects roughly 25 percent of people in the U.S. There is no drug treatment for the disease, although weight loss can reduce the buildup of fat in the liver.
Now, studying mice, new research shows that a natural sugar called trehalose prevents the sugar fructose — thought to be a major contributor to nonalcoholic fatty liver disease — from entering the liver and triggers a cellular housekeeping process that cleans up excess fat buildup inside liver cells.
The research, by a team at Washington University School of Medicine in St. Louis, appears Feb. 23 in the journal Science Signaling.
“In general, if you feed a mouse a high-sugar diet, it gets a fatty liver,” said first author Brian J. DeBosch, MD, PhD, a pediatric gastroenterologist. “We found that if you feed a mouse a diet high in fructose plus provide drinking water that contains three percent trehalose, you completely block the development of a fatty liver. Those mice also had lower body weights at the end of the study and lower levels of circulating cholesterol, fatty acids and triglycerides.”
Evidence suggests that nonalcoholic fatty liver disease develops as the liver works hard to process dietary sugar, especially fructose, found naturally in fruit but also added as high-fructose corn syrup to soft drinks and many processed foods. Ultimately, the body stores fructose in the liver as fats called triglycerides. In severe cases of the disease, the fat can build up to toxic levels that may eventually require a liver transplant.
Trehalose is a natural sugar found in plants and insects and consists of two glucose molecules bound together. While it is approved by the Food and Drug Administration for human consumption, DeBosch cautions that more research is required before trehalose could be tested in people with nonalcoholic fatty liver disease as part of a clinical trial.
“I can’t recommend it to my patients yet,” said DeBosch, who sees patients at St. Louis Children’s Hospital. “We know the mice that received drinking water with three percent trehalose lost weight, and we suspect that weight loss was due to loss of fat, but we can’t be certain that’s the only effect. We need more studies to make sure they were not losing bone or muscle mass.”
In the meantime, DeBosch advises his patients to avoid foods with added fructose, especially sugar-sweetened beverages.
The role of dietary sugar in nonalcoholic fatty liver disease has been implicated in conditions such as obesity, insulin resistance and high blood pressure, among other markers of metabolic syndrome. So it might seem counterintuitive to treat a condition that appears to be caused at least in part by sugar consumption, with more sugar. But the effect of trehalose on fructose transport into the liver gives some clues to how it works.
In previous research, DeBosch and his colleagues, including senior author Kelle H. Moley, MD, the James P. Crane Professor of Obstetrics and Gynecology, showed that a protein on the surface of liver cells called GLUT8 is required for mice to develop fatty livers in response to a high-fructose diet.
“We knew that GLUT8 carries large amounts of fructose into liver cells,” DeBosch said. “So we looked for things that block GLUT8. We were interested in investigating trehalose because it has been studied in models of neurodegenerative disorders such as prion disease or amyotrophic lateral sclerosis — Lou Gehrig’s disease. In mice, trehalose appears to cause brain cells to swallow up abnormal proteins that accumulate in these conditions. We wondered if it would do the same for fat buildup in liver cells.”
DeBosch and his colleagues showed that trehalose blocks the transport of energy in the form of sugar into liver cells, causing the cells to behave as if they’re starving. When a cell is in a state of starvation, it can turn on a process called autophagy, or self-eating, and begin to consume the fat already stored in the cell. But the process is not specific to fat and can drain cells of proteins, sugars and other waste.
“We appear to be hijacking the liver’s own starvation pathway using a sugar already found in nature,” DeBosch said. “We think autophagy may be triggered when the cell is stressed with too much fat or protein buildup. The cell turns on autophagy in response to the stress or because of a lack of energy and starts gobbling stuff up. It’s a house cleaning.”
DeBosch expects that other researchers may turn their attention to trehalose in order to understand exactly how this sugar hijacks cell signaling pathways. DeBosch also said the potential for this treatment strategy goes further than neurodegenerative and metabolic diseases.
“Autophagy plays numerous roles in the body, ranging from healthy development to involvement in cancer and autoimmunity,” DeBosch said. “The hope is that by studying this ‘nutraceutical’ and its actions, we can uncover and then leverage its important cellular activities to halt or reverse disease.”
This work was supported by the Washington University Child Health Research Center, grant number K12HD076224; the Children’s Discovery Institute, grant number MI-FR-2014-426; the Robert Wood Johnson Foundation; the AGA-Gilead Sciences Research Scholar Award in Liver Disease; the Pediatric Scientist Development Program, grant number K12HD000850-29; the Nutrition & Obesity Research Center, grant number P30DK056341; the Washington University Digestive Disease Research Core Center, grant number P30DK52574; the Administration and Resource Access Core, the Advanced Imaging and Tissue Analysis Core, and the Murine Models core, grant numbers, HL-38180, DK-56260 and R01-DK078187; the American Heart Association, grant number 14PRE18320006; the Washington University Spencer T. Olin Fellowship; the Washington University NIGMS Institutional Training Grant in Cell and Molecular Biosciences, grant number T32GM007067; and the Washington University Biomedical Mass Spectrometry Research Facility, grant numbers P41 GM103422 and P30 DK020579.
DeBosch BJ, Heitmeier M, Mayer AL, Higgins CB, Crowley J, Kraft T, Chi M, Newberry E, Chen Z, Finck BN, Davidson NO, Yarasheski KE, Hruz PW, Moley KH. Trehalose inhibits solute carrier 2A (SLC2A) proteins to induce autophagy and prevent hepatic steatosis. Science Signaling. Feb. 23, 2016.
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