Shared mechanistic pathways of glucagon signalling: Unlocking its potential for treating obesity, metabolic dysfunction-associated steatotic liver disease, and other cardio-kidney-metabolic conditions.
Neff. Guy W GW
Key Findings
- Glucagon influences metabolism, appetite, and fat burning beyond just raising blood sugar
- Multi‑agonist drugs that activate both glucagon and GLP‑1 receptors cause significant weight loss and improve liver health in early human studies
- Safety, long‑term effects, and exact pathways of chronic glucagon activation are still unknown
Practical Outcomes
- Watch for phase‑3 trial results on retatrutide and similar compounds, as they may become powerful tools for weight and liver health management. Until they’re approved, consider existing GLP‑1 agonists for similar benefits, but stay aware of potential future protocols that combine glucagon activity for enhanced metabolic effects.
Summary
New drugs that mix glucagon and GLP‑1 signals, like retatrutide, are showing big weight‑loss and liver‑health benefits in early trials. They work by boosting metabolism, burning fat, and cutting appetite, while the GLP‑1 part keeps blood sugar in check. The long‑term safety and exact mechanisms are still being studied, but the results look promising for tackling obesity and fatty‑liver disease.
Abstract
Glucagon is a pancreatic peptide hormone whose receptor (GCGR) is expressed in the liver, kidney, and, to a lesser extent, various other tissues. Glucagon is well known as the counterpart to insulin in glucose homeostasis. However, recent evidence has revealed other potential roles of glucagon, which include the regulation of amino acid metabolism via a liver-pancreatic alpha cell axis, stimulation of lipolysis and mitochondrial fat oxidation in the liver (and possibly in other tissues), reduction of caloric intake, and an increase in energy expenditure (at least in animal models). These advances in basic science-together with clinical trials that found GCGR antagonists increased body weight, hepatic fat, and serum lipids in people with type 2 diabetes-are driving the development of GCGR-based agonists for the treatment of obesity, metabolic dysfunction-associated steatotic liver disease (MASLD), and other cardio-kidney-metabolic diseases. Due to the hyperglycaemic effects of glucagon, these unimolecular compounds also incorporate moieties that activate the glucagon-like peptide-1 (GLP-1) receptor, which stimulates insulin secretion to lower blood glucose levels. In early clinical trials, several GCGR-based multi-agonists (mazdutide, survodutide [being developed by the sponsor of this review], retatrutide) demonstrated substantial efficacy for eliciting weight loss in people with obesity while improving liver health in those with MASLD. However, the physiological and molecular pathways modulated by chronic pharmacological activation of the GCGR in humans remain to be delineated, as do its potential risks. Thus, there is great interest in the ongoing phase 3 clinical trials of these compounds. As data for their safety and efficacy emerge, glucagon's role in energy regulation and lipid metabolism will become clearer, along with warranting a potential new therapeutic option for obesity and MASLD.
Study Information
pubmed
2025
2025-09-30T00:00:00.000Z
10.1111/dom.70148
154