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Exercise in pill form

Researchers to examine receptors of muscle metabolism

Drs John Walker (back) and Thomas Burris (Credit: Saint Louis University)
The scientists will optimise two promising drug compounds, moving a step closer toward capturing the benefits of exercise in pill form

Researchers at Saint Louis University will tackle the twin epidemics of diabetes and obesity by tapping into the potential of two nuclear receptors that control muscle metabolism. The scientists will optimise two promising drug compounds, moving a step closer toward capturing the benefits of exercise in pill form.

Dr Thomas Burris, chair of pharmacology and physiology at Saint Louis University, and Dr John Walker, assistant professor of pharmacology and physiology at Saint Louis, have received US$2.4 million from the US Department of Defense and US$1.74 million from the National Institutes of Health in a series of grants that will fund the study of two receptors that are linked to muscle metabolism: REV-ERB and ERR.

In past studies, a drug developed by Burris that targets REV-ERB appears to act as an exercise mimic. Genetic studies with ERR suggest that it may be a good target for development of exercise mimetic drugs as well. Aiming to offer new options for patients suffering from the burdens of these health threats, Burris and Walker's work combines chemistry and biology to develop new treatments.

"We can design drugs rather than just study them," said Burris. "That's the fun part. We can take the work further toward developing new therapies."

Exercise provides health benefits that include improving insulin sensitivity and weight control. But not everyone is able to exercise.

"If you exercise, it's effectively a treatment for diabetes and obesity as you increase the metabolic rate of muscle," he added. "You develop a more efficient muscle. That's what you get from exercise. You develop more endurance and that is good for your metabolic function. Our drug compounds are doing similar things. They make muscles look like they're exercising, turning on the genes that get activated during exercise, even if no exercise is happening. Both studies operate this way."

Burris and Walker study nuclear receptors, which are signalling molecules that sense different hormone levels and regulate gene expression based on the signal they receive. The cancer drug tamoxifen, contraception, a heart failure drug and thyroid replacement therapy all work by targeting nuclear receptors.

"In many cases of illness, signalling is off," he explained. "And we can correct signals by dialling the hormone messages up or down, mimicking hormones or blocking them."

In both studies, researchers aim to optimize drug compounds to dial up muscle metabolism.

REV-ERB

Burris and his team were the first to use a synthetic agonist (a drug designed to turn the action up) for REV-ERB to show that it caused weight loss and improved metabolic function in animals.

As the research team optimises the drug for diabetes and obesity, they are looking to maximise some effects they've already noticed. In past studies, they've seen multiple benefits to the metabolic state, with improved cholesterol and reduced atherosclerosis, including some direct effects on plaques, and lower inflammation. They saw mice lose weight, even on high fat diets, use more oxygen, expend more energy and show greater endurance.

"Nuclear receptors are typically very good drug targets," said Burris. "However, because they control gene transcription, they are tricky. Though we want to discover how to turn a receptor up or down, it's important to find a ligand that won't do too much, which could cause side effects."

A key task for Walker - a chemist - is to prevent the drug from crossing the blood-brain barrier, the body's natural division that separates the brain from blood circulating in the body. This is the reverse challenge that many drug-designers face. Often, it's most difficult to help drugs intended to reach the brain cross the barrier.

However, in past studies, REV-ERB appeared to have effects on the brain, including decreasing anxiety. While researchers would like to tap the receptor's potential in the mental health arena as well, they also want to ensure that a drug designed to help obesity and diabetes is limited in its scope.

"The effects we see in the brain are not necessarily show-stoppers but since there are some, we want to try to stop the drug from reaching the brain," he added. "We don't necessarily want to decrease anxiety in someone who doesn't need it."

In addition to addressing the blood-brain barrier issue, Burris and Walker look to optimize the compound in other ways, including testing for any toxic properties and developing once-a-day dosing.

ERR

In the second study, Burris and Walker will optimise compounds that target a different receptor, ERR. ERR is an orphan receptor, meaning scientists don't know what its natural ligand is. A ligand is the molecule that binds to the receptor and regulates its activity. A few synthetic ligands have been created, but they are not yet perfected for use in disease models.

The SLU researchers will take this work further, aiming to develop methods to turn up the volume on ERR.

"We've designed some agonists to see what their effect is," Walker said. "Most of the data suggests that more ERR is better, the most useful in terms of muscle metabolism. These agonists look as though they'll be useful in models of obesity and diabetes."

In addition to showing promise for obesity and diabetes, the study will examine how improvements to muscle metabolism may affect muscular dystrophy.

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