A molecule combining the properties of two endocrine hormones could be an effective treatment for adult on-set diabetes and obesity, according to researchers from Indiana University (IU) and international collaborators including an Australian scientist.

The research, which included clinical trials with human subjects as well as detailed laboratory studies with rodents and monkeys, tested a synthetic drug that activates receptors for two gut hormones called incretins. It was published online in late October 2013 in the journal Science Translational Medicine.

The researchers have previously published positive preclinical results for other targeted peptide treatments, but this study marks the first time the results have extended to clinical trials in humans.

The results showed that the drug may lower body weight and reduce diabetes. The two naturally occurring peptide hormones, known as GLP-1 and GIP are instrumental to the body’s regulation of metabolism.

“The results demonstrate that GLP-1 and GIP, when built into a single molecule, provide synergistic activity to control glucose and lower body weight across a spectrum of animal models, including in human clinical experiments,” said Richard DiMarchi, Chemist at Indiana University Bloomington.

The study continues a longtime collaboration between Professor DiMarchi, the Standiford H. Cox Distinguished Professor of Chemistry and the Linda and Jack Gill Chair in Biomolecular Sciences in the IU Bloomington College of Arts and Sciences, and Professor Matthias Tschöp, director of the Institute for Diabetes and Obesity at the Helmholtz Zentrum München, Germany.

Lead authors of the study, Brian Finan and Ma Tao, are both formerly of DiMarchi’s lab at IU Bloomington. Dr Finan now works with the Institute for Diabetes and Obesity at the Helmholtz Zentrum München. Tao is with Beijing Hanmi Pharmaceutical in China. Co-authors, in addition to Professor DiMarchi and Professor Tschöp, include Bloomington scientists David Smiley, Vasily Gelfanov and Bin Yang.

“The integrated combinatorial action of these two physiological hormones provides a unique and beneficial approach to treating the metabolic syndrome,” Dr Finan said. “It represents an important step forward in our search for more effective therapeutic options,” he said.

Research is “important progress” in search for obesity and diabetes treatment

Researchers said the study showed “important progress” in the effort to find effective treatments to address what health authorities say is a global epidemic of obesity and Type 2 diabetes along with the metabolic syndrome, which consists of obesity associated with factors such as high blood pressure, high triglycerides, hyperglycemia and low HDL cholesterol.

According to the International Diabetes Federation, as much as 20 percent of the world’s adults have some form of the metabolic syndrome, making them far more vulnerable to heart attack and stroke than people without the syndrome.

New drug could be given in smaller doses

The higher potency of the combined molecule suggests it could be administered at lower doses than previously developed medications, reducing side effects such as nausea and vomiting.

“Currently approved drugs are quite effective,” Professor DiMarchi said. “But they are insufficient in normalising glucose, and they certainly don’t cause much loss of body weight,” he said.

Best-in-class medications, such as the drugs trademarked as Byetta and Victoza, target GLP-1 receptors. But previous studies involving GIP have produced conflicting results, with some suggesting that activating GIP receptors can increase rather than reduce weight gain. According to Professor DiMarchi, the current study demonstrates clearly that combining GLP-1 and GIP can produce improved therapeutic effects.

The research included extensive studies with animals, including mice, rats and monkeys. The combination molecule proved considerably more effective than currently approved medications in controlling blood glucose and reducing weight. In some outcomes, it achieved results comparable to those that resulted from a 10-fold higher dose of agents that target only GLP-1 receptors.

Clinical trials conducted by Roche produced a decrease in glucose levels beyond what would be expected from conventional medicines. The six-week trial was not of significant duration to provide definitive evidence about weight loss in humans.

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