Disruption of Glucagon-Like Peptide 1 Signaling in Sim1 Neurons Reduces Physiological and Behavioral Reactivity to Acute and Chronic Stress

Organismal stress initiates a tightly orchestrated set of responses involving complex physiological and neurocognitive systems. Here, we present evidence for glucagon-like peptide 1 (GLP-1)-mediated paraventricular hypothalamic circuit coordinating the global stress response. The GLP-1 receptor (Glp...

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Veröffentlicht in:The Journal of neuroscience 2017-01, Vol.37 (1), p.184-193
Hauptverfasser: Ghosal, Sriparna, Packard, Amy E.B., Mahbod, Parinaz, McKlveen, Jessica M., Seeley, Randy J., Myers, Brent, Ulrich-Lai, Yvonne, Smith, Eric P., D'Alessio, David A., Herman, James P.
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Sprache:eng
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Zusammenfassung:Organismal stress initiates a tightly orchestrated set of responses involving complex physiological and neurocognitive systems. Here, we present evidence for glucagon-like peptide 1 (GLP-1)-mediated paraventricular hypothalamic circuit coordinating the global stress response. The GLP-1 receptor (Glp1r) in mice was knocked down in neurons expressing single-minded 1, a transcription factor abundantly expressed in the paraventricular nucleus (PVN) of the hypothalamus. Mice with single-minded 1-mediatedGlp1rknockdown had reduced hypothalamic-pituitary-adrenal axis responses to both acute and chronic stress and were protected against weight loss associated with chronic stress. In addition, regionalGlp1rknockdown attenuated stress-induced cardiovascular responses accompanied by decreased sympathetic drive to the heart. Finally,Glp1rknockdown reduced anxiety-like behavior, implicating PVN GLP-1 signaling in behavioral stress reactivity. Collectively, these findings support a circuit whereby brainstem GLP-1 activates PVN signaling to mount an appropriate whole-organism response to stress. These results raise the possibility that dysfunction of this system may contribute to stress-related pathologies, and thereby provide a novel target for intervention.
ISSN:0270-6474
1529-2401
DOI:10.1523/JNEUROSCI.1104-16.2017