A new molecule to improve treatment for type 2 diabetes and non-alcoholic fatty liver disease
A new molecule, EPB-53, could help fight type 2 diabetes and non-alcoholic fatty liver disease, according to a new study led by the team of Manuel Vázquez-Carrera, from the Faculty of Pharmacy and Food Sciences and the Institute of Biomedicine of the University of Barcelona (IBUB), and the Diabetes and Associated Metabolic Diseases Networking Biomedical Research Centre (CIBERDEM).
Other participants in the study, published in the journal British Journal of Pharmacology, are the members of the teams led by the researchers Francesc Villarroya, from the Faculty of Biology and the Institute of Biomedicine of the University of Barcelona (IBUB) and member of the Physiopathology of Obesity and Nutrition Networking Biomedical Research Centre (CIBERobn) and the Research Institute Sant Joan de Déu; and Santiago Vázquez, from the Pharmaceutical Chemistry Unit of the Faculty of Pharmacy and Food Sciences of the UB and IBUB.
Diabetes: research on active drugs orally administrated
The FGF21 hormone –the fibroblast growth factor 21- is an endocrine factor with a determining role in the energetic metabolism as an anti-diabetes and anti-obesity agent. This hormone is regarded as a potential therapeutic target to treat type 2 diabetes and non-alcoholic fatty liver disease, which usually occur due obesity and insulin resistance. However, the FGF21 analogue compounds that showed pharmaceutical activity in animal models require subcutaneous injection, and can generate adverse effects (loss of bone mass, increase of heart rate and arterial pressure, etc.).
According to the new preclinical study, levels of FGF21 in the liver and plasma can increase through oral administration of the EPB-53 molecule. "This effect is possible because EPB-53 is a molecule that activates HRI (eIF2α kinase regulated by hemo group), a kinase that can boost a factor of transcription involved in the increae of FGF21, which reduces glucose tolerance and hepatic steatosis in mice which are fed with a fat-rich diet," says researcher Manuel Vázquez-Carrera, from the Department of Pharmacology, Toxicology and Therapeutical Chemistry of the UB.
The conclusions of the study prove the use of FGF21 inducer compounds could lead to new therapeutic strategies to treat type 2 diabetes and non-alcoholic fatty liver disease, similarly to what analogue compounds do subcutaneously.
"In addition, we hope to see in future studies that these would not cause adverse effects that have been described in some FGF21 analogues. Therefore, we are working on the development of new HRI activators with better pharmacokinetic characteristics for the treatment of type 2 diabetes such as non-alcoholic steatohepatitis," says Vázquez-Carrera.
The incidence of type 2 mellitus diabetes has grown among the population over the last years and the available drugs cannot control the progress of the disease in all patients. Also, non-alcoholic fatty liver disease affects one out of four people and the worst variant, non-alcoholic steatohepatitis, does not have any specific approved drug. Finding new drugs for oral administration is, thus, one of the challenges in biomedicine to improve health care for millions of people worldwide who are affected by these metabolic diseases.