Physicians have used the drug metformin to treat type 2 diabetes for more than half a century, but despite its prevalence, researchers have lacked a clear understanding of how it works. Now, Yale researchers have elucidated the mechanism behind metformin and related type 2 diabetes drugs, and debunked a previously held theory on how they work. The team, including senior author Gerald Shulman, MD, Ph.D., George R. Cowgill Professor of Medicine (Endocrinology) and professor of cellular and molecular physiology, and first author Traci LaMoia, a graduate student in Shulman’s lab, published their findings in PNAS on March 1.
“Metformin is the most commonly used drug to treat diabetes,” says Shulman. “It’s important to understand how it works so we can potentially develop even better drugs to treat type 2 diabetes.”
Studies in humans have shown that metformin inhibits the process of gluconeogenesis, which is how the liver makes glucose from non-glucose precursors such as amino acids and lactate. How it accomplishes this, however, has been a mystery.
Mitochondria in cells generate energy through the electron transport chain, which consists of four protein complexes that release energy through a series of reactions. Most scientists previously believed that metformin works by inhibiting complex I, the first and largest of the mitochondrial complexes that creates the hydrogen ion gradient. However, Shulman’s group has previously demonstrated that metformin only inhibits complex I at much higher pharmacological concentrations than what is typically prescribed.
To further test this hypothesis, the team performed a series of experiments both in liver slices and in mice. Using a complex I inhibitor known as piercidin A, they found that this mechanism failed to reduce liver gluconeogenesis. “Using a very specific inhibitor of complex I, we show that complex I inhibition doesn’t reduce blood glucose in both in vitro and in vivo studies,” says Shulman.
Progress through research
Through earlier studies, Shulman’s lab team had identified the inhibition of the mitochondrial-associated enzyme glycerol phosphate dehydrogenase, which converts glycerol to glucose, as a potential mechanism for metformin action. Now, in the current study, they were able to show through another series of experiments that metformin, as well as the related drugs phenformin and galegine, did in fact inhibit glycerol conversion to glucose both in vitro and in vivo and that they did so through an indirect mechanism by inhibiting complex IV activity.
“Taken together these studies show that metformin does not lower blood glucose by inhibition of complex I activity, but instead it reduces blood glucose through inhibition of complex IV activity which in turn leads to inhibition of glycerol phosphate dehydrogenase activity and reductions in glycerol conversion to glucose” says Shulman.
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