«In our study,
the hyperglycemic mice had increased bone resorption [the breakdown and absorption of old bone], which outpaced the formation of new bone.
In a study published in Nature Communications, the investigators report that
hyperglycemic mice (or mice with type 2 diabetes) have a 24-fold higher accumulation of succinate, an intermediate metabolite, in the metabolic pathways of their bone marrow stromal cells.
Not exact matches
In the study, «Succinate and its G - protein - coupled receptor stimulate osteoclastogenesis,» the researchers took samples of bone marrow from
hyperglycemic male
mice and healthy
mice.
Paternal stress epigenetically downregulates miR - 466b - 3p expression, leading to increased PEPCK expression and hepatic gluconeogenesis in
hyperglycemic F1
mice.
In a chronic sleep deprivation experiment, young
mice were sensitized to insulin and had improved control of their blood sugar, whereas aged animals became
hyperglycemic and failed to maintain appropriate plasma insulin concentrations.
Adoptive transfer of these cells resulted in reversion of the
hyperglycemic state in NOD
mice, with reduced T cell infiltrates in the pancreas and increased circulating FoxP3 + regulatory T cells.
At 8 months of age, both DIO and DR groups had increased
hyperglycemic response during a glucose tolerance test, which was normalized in 16 - month - old
mice.
The healthy
mice developed low - grade intestinal inflammation and a metabolic disorder that caused them to eat more, becoming obese,
hyperglycemic, and resistant to insulin.