Better drugs to tackle diabetes and obesity

“This knowledge can guide how to change potential new drugs to capture beneficial differences in signalling that may better treat disease,” says project lead, Dr Denise Wootten of the Drug Discovery Biology theme at the Monash Institute of Pharmaceutical Sciences (MIPS).

Diabetes is a wide-spread chronic illness that can lead to major organ failure and death, and globally affects nearly 10% of the population,[1] with incidence of the disease rising in parallel with the large increase in obesity. In Australia, the incidence rates are even higher for Aboriginal and Torres Strait Islander peoples.

Common diabetes drugs such as Byetta and Victoza act via the GLP-1R receptor by mimicking the natural hormone for this receptor. Drugs that target GLP-1Rs have also been approved for treatment of obesity and are in clinical trials for treatment of neurodegenerative disorders, including Alzheimer’s and Parkinson’s disease.

However, the interaction process between drug and receptor has remained largely unclear, until now. “What we are learning is that these drugs can have distinct actions via the GLP-1R and that these differences, termed ‘biased agonism’, can lead to differential therapeutic effects,” says Professor Sexton, Head of the Drug Discovery Biology theme at MIPS.

A recently discovered analogue of the drug Byetta, ‘exendin-P5’ is one such ‘biased agonist’, as it interacts differently with the receptor than current approved GLP-1R drugs.

Exendin-P5 was recently shown to reduce blood glucose levels in animal models of diabetes, but with a distinct mode of action from approved GLP-1R drugs that could eventually lead to better patient outcomes in controlling blood glucose levels.

The announcement follows the launch of Cincera Therapeutics, a company targeting therapies for obesity and diabetes underpinned by Monash University research.

Discover more here.

Image credit: Monash University.