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Study finds new therapeutic targets to fight against type 2 diabetes

June 08,2024

Barcelona: The fact that individuals with type 2 diabetes have elevated fasting glucose levels is among the most perplexing factors for them. This is due to the fact that in these insulin-resistant individuals, the liver produces glucose, a process that still raises many unanswered issues for scientists.

The most significant developments in our knowledge of this mechanism are now presented in a review paper that was published in the journal Trends in Endocrinology & Metabolism. In the battle against type 2 diabetes mellitus, which the World Health Organization (WHO) lists as one of the pandemics of the twenty-first century, it also aids in the discovery of novel therapeutic targets.

The UB Institute of Biomedicine (IBUB), the Sant Joan de Deu Research Institute (IRSJD), the Faculty of Pharmacy and Food Sciences at the University of Barcelona, the Centre for Biomedical Research Network on Diabetes and Associated Metabolic Diseases (CIBERDEM), and Professor Manuel Vazquez-Carrera are the study’s leaders. Experts Emma Barroso, Javier Jurado-Aguilar, and Xavier Palomer (UB-IBUB-IRJSJD-CIBERDEM) as well as Professor Walter Wahli from the University of Lausanne (Switzerland) are involved in the work.

Type 2 diabetes mellitus is an increasingly common chronic disease that results in high levels of circulating glucose — the cellular energy fuel — due to a deficient insulin response in the body. It can cause severe organ damage and is estimated to be under-diagnosed in a high percentage of the affected population worldwide.

In patients, the glucose synthesis pathway in the liver (gluconeogenesis) is hyperactivated, a process that can be controlled by drugs such as metformin. “Recently, new factors involved in the control of hepatic gluconeogenesis have been identified. For example, a study by our group revealed that growth differentiation factor (GDF15) reduces the levels of proteins involved in hepatic gluconeogenesis”, says Professor Manuel Vazquez-Carrera, from the UB’s Department of Pharmacology, Toxicology and Therapeutic Chemistry.

To make progress in the fight against this pathology, it will also be necessary to further study pathways such as TGF-b, which is involved in the progression of metabolic dysfunction-associated fatty liver disease (MASLD), a very prevalent pathology that often coexists with type 2 diabetes mellitus. “TGF-b plays a very relevant role in the progression of liver fibrosis and has become one of the most important factors that may contribute to increased hepatic gluconeogenesis and, therefore, to type 2 diabetes mellitus. Therefore, studying the involvement of the TGF-b pathway in the regulation of hepatic gluconeogenesis could help to achieve better glycaemic control”, stresses Vazquez-Carrera.

However, acting on a single factor to improve the regulation of gluconeogenesis does not seem to be a sufficient therapeutic strategy to adequately control the disease.

“It would be important to be able to design combination therapies that could consider the different factors involved to improve the approach to type 2 diabetes mellitus”, Vazquez-Carrera says.

“Today there are several molecules — TGF-b, TOX3, TOX4, etc. — that could be considered therapeutic targets for designing future strategies to improve patients’ well-being. Their efficacy and safety will determine their therapeutic success. We cannot lose sight of the fact that controlling the overactivation of hepatic gluconeogenesis in type 2 diabetes mellitus has an additional difficulty: it is a key pathway for making glucose available in fasting situations, it is finely modulated by numerous factors and this makes regulation difficult”, he adds.

Interestingly, other factors involved in the control of gluconeogenesis have also been identified in patients hospitalised with COVID-19 who showed high glucose levels. “Hyperglycaemia was very prevalent in patients hospitalised with COVID-19, which seems to be related to the ability of SARS-CoV-2 to induce the activity of proteins involved in hepatic gluconeogenesis”, the expert notes.

The mechanisms of action of metformin, the most commonly prescribed drug for the treatment of type 2 diabetes, which reduces hepatic gluconeogenesis, are still not fully understood. It has now been discovered that the drug decreases gluconeogenesis via inhibition of complex IV of the mitochondrial electron transport chain. This is a mechanism independent of the classical effects known until now through activation of the AMPK protein, a sensor of the cell’s energy metabolism.

“Inhibition of mitochondrial complex IV activity by metformin — not complex I as previously thought — reduces the availability of substrates required for hepatic glucose synthesis”, says Vazquez-Carrera.

In addition, metformin can also reduce gluconeogenesis through its effects on the gut, leading to changes that ultimately attenuate hepatic glucose production in the liver. “Thus, metformin increases glucose uptake and utilisation in the gut, and generates metabolites capable of inhibiting gluconeogenesis when they reach the liver via the portal vein. Finally, metformin also stimulates the secretion of GLP-1 in the intestine, a hepatic gluconeogenesis inhibitory peptide that contributes to its anti-diabetic effect”, he explained. (ANI)

Source: Healthworld

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