Year: 2024
Type: article
Abstract: Chronic stress has been shown to induce hyperglycemia in both peripheral blood and the brain, yet the detailed mechanisms of glucose metabolism under stress remain unclear. Utilizing 13C6-labeled glucose to trace metabolic pathways, our study investigated the impact of stress by chronic social defeat (CSD) on glucose metabolites in the liver and brain one week post-stress. We observed a reduction in 13C6-enrichment of glucose metabolites in the liver, contrasting with unchanged levels in the brain. Notably, hepatic glycogen levels were reduced while lactate concentrations were elevated, suggesting lactate as an alternative energy source during stress. Long-term effects were also examined, revealing normalized blood glucose levels and restored glycogen stores in the liver three weeks post-CSD, despite sustained increases in food intake. This normalization is hypothesized to result from diminished glucagon levels leading to reduced glycogen phosphorylase activity. Our findings highlight a temporal shift in glucose metabolism, with hyperglycemia and glycogen depletion in the liver early after CSD, followed by a later phase of metabolic stabilization. These results underscore the liver’s critical role in adapting to CSD and provide insights into the metabolic adjustments that maintain glucose homeostasis under prolonged stress conditions.
Source: Scientific Reports
Authors: Fabiënne S. Meijboom, Annika Hasch, Inigo Ruiz de Azua, Camila Takeno Cologna, Shauni Loopmans, Beat Lutz, Marianne B. Müller, Bart Ghesquière, Michael A. van der Kooij
Institutions: Utrecht University, University Medical Center Utrecht, Wilhelmina Children's Hospital, Leibniz Institute for Resilience Research, Johannes Gutenberg University Mainz, University Medical Center of the Johannes Gutenberg University Mainz, VIB-KU Leuven Center for Cancer Biology, KU Leuven
Language: English
Subfield: Behavioral Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,590
Funder: Deutsche Forschungsgemeinschaft
Award: G3429082103
OpenAlex ID: W4403784863
