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Publication : Glucocorticoid feedback uncovers retrograde opioid signaling at hypothalamic synapses.

First Author  Wamsteeker Cusulin JI Year  2013
Journal  Nat Neurosci Volume  16
Issue  5 Pages  596-604
PubMed ID  23563581 Mgi Jnum  J:197687
Mgi Id  MGI:5494341 Doi  10.1038/nn.3374
Citation  Wamsteeker Cusulin JI, et al. (2013) Glucocorticoid feedback uncovers retrograde opioid signaling at hypothalamic synapses. Nat Neurosci 16(5):596-604
abstractText  Stressful experience initiates a neuroendocrine response culminating in the release of glucocorticoid hormones into the blood. Glucocorticoids feed back to the brain, causing adaptations that prevent excessive hormone responses to subsequent challenges. How these changes occur remains unknown. We found that glucocorticoid receptor activation in rodent hypothalamic neuroendocrine neurons following in vivo stress is a metaplastic signal that allows GABA synapses to undergo activity-dependent long-term depression (LTDGABA). LTDGABA was unmasked through glucocorticoid receptor-dependent inhibition of Regulator of G protein Signaling 4 (RGS4), which amplified signaling through postsynaptic metabotropic glutamate receptors. This drove somatodendritic opioid release, resulting in a persistent retrograde suppression of synaptic transmission through presynaptic mu receptors. Together, our data provide new evidence for retrograde opioid signaling at synapses in neuroendocrine circuits and represent a potential mechanism underlying glucocorticoid contributions to stress adaptation.
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