Working in mice, the researchers showed they could reduce glucose production in the liver and lower blood sugar levels
Scientists have found a new way to lower blood sugar levels by reducing glucose production in
the liver, paving the way for more effective drugs for type II diabetes. According to a report in PTI, some treatments for type II diabetes make the body more sensitive to insulin, the hormone that lowers blood sugar. But new research at Washington University School of Medicine in St Louis suggests a different strategy: slowing the production of glucose in the liver.
Working in mice, the researchers showed they could reduce glucose production in the liver and lower blood sugar levels. They did so by shutting down a liver protein involved in making glucose, an approach that may work in patients with type II diabetes.
“We think this strategy could lead to more effective drugs for type II diabetes,” said principal investigator Brian N Finck, Associate Professor of medicine in the Division of Geriatrics and Nutritional Science.
“A drug that shuts down glucose production has the potential to help millions of people affected by the most common form of diabetes,” said Finck.
Finck worked with researchers at the University of Texas Southwestern Medical Centre and the biopharmaceutical company Metabolic Solutions Development Co. The company is involved in clinical trials that are evaluating the drug compound MSDC-0602 as a treatment for diabetes.
The new study demonstrates that the compound works, at least in part, by inhibiting a protein that’s key to glucose production in the liver. The research team, led by first author Kyle S McCommis, a
postdoctoral research scholar, cut sugar production in liver cells by inhibiting a key protein involved in transporting pyruvate, a building block of glucose, from the bloodstream into the energy factories of liver cells, called mitochondria.
Previous research had suggested interfering with pyruvate may limit glucose production in the liver, but this study is the first to demonstrate the critical role played by the pyruvate transport protein.
In addition to diabetes, the researchers also think that interfering with pyruvate transport may help patients with non-alcoholic fatty liver disease, a condition common in people with obesity.