ePosters
The central nucleus of the amygdala (CeA), or the “nociceptive amygdala” is key in chronic pain processing1,2. A major subclass of CeA neurons expressing corticotropin-releasing hormone (CRH; CeA-CRH neurons) is sensitized in acute, but not chronic, neuropathic pain3. Signal transduction regulation of CeA-CRH neurons remains poorly understood, which we addressed by investigating sphingosine-1-phosphate (S1P). S1P has region-specific effects on pain in the CNS4,5. I hypothesized S1P regulates synaptic activity onto CeA-CRH neurons in neuropathic pain.
Regan C. Hines, n/a
PhD Candidate
Indiana University School of Medicine Department of Pharmacology & Toxicology
Indianapolis, Indiana, United States
Patrick L. Sheets, PhD
Associate Professor
Indiana University School of Medicine Department of Pharmacology & Toxicology, United States