MechanismsAnimals

Aged mice had high levels of a hormone that raises blood sugar

Experiments found increased release of the hormone in aged mice with normal or reduced responses to insulin, which lowers blood sugar.

Pancreatic cells above laboratory mice and paired tissue samples, with a larger cell cluster and denser released granules on the right.

Aging Cell

In an animal experiment, researchers studied aged mice with normal sensitivity or resistance to insulin, a hormone that lowers blood sugar. They examined pancreatic alpha cells, which release glucagon, a hormone that raises blood sugar. Both groups had high blood glucagon levels and increased glucagon release. Tests outside the animals linked these changes to a greater total mass of alpha cells, higher glucagon content and poorer suppression of glucagon release. Most changes were already present in mice with normal insulin sensitivity but were generally more pronounced with insulin resistance.

A separate analysis of the CORDIOPREV clinical study found high blood glucagon in older adults with insulin resistance. Older people with higher blood glucagon also had a higher risk of developing type 2 diabetes.

Why it matters

Blood sugar control depends on both insulin and glucagon. The findings point to glucagon-producing cells as contributors to impaired blood sugar control and diabetes associated with aging.

Caveats

The main findings came from experiments in mice, not people. The human analysis linked glucagon levels to diabetes risk but did not establish cause and effect.

The paper

Aging Affects Pancreatic α-Cell Function and Promotes Hyperglucagonemia: Implications in Age-Associated Diabetes

Eva Tudurí, Lucía Almagro, Ana Ojeda-Rodríguez,
Show 14 more authorsRaquel Pascua-Maestro, Henver S Brunetta, Sergi Soriano, Alejandro López-Moreno, Talía Boronat-Belda, Sergio Velasco-Avilés, Joel Alves da Silva Junior, Manuel Castellano-Muñoz, Alex Rafacho, Irene Cózar-Castellano, Ángel Nadal, Paloma Alonso-Magdalena, Beatriz Merino, José López-Miranda,
Ivan Quesada

Instituto de Investigación

Aging Cell · 1 Oct 2026

doi.org/10.1111/acel.70753PubMed 42836454