4.8 Article

A Neural Circuit for the Suppression of Pain by a Competing Need State

Journal

CELL
Volume 173, Issue 1, Pages 140-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.02.057

Keywords

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Funding

  1. University of Pennsylvania School of Arts and Sciences
  2. American Heart Association (AHA) [17SDG33400158]
  3. Whitehall Foundation
  4. NIH [1R01DK114104, 2T32DK7314-36, F32DK112561-01, R01DK114812]
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [F32DK112561, R01DK114104, T32DK007314, R01DK112812] Funding Source: NIH RePORTER

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Hunger and pain are two competing signals that individuals must resolve to ensure survival. However, the neural processes that prioritize conflicting survival needs are poorly understood. We discovered that hunger attenuates behavioral responses and affective properties of inflammatory pain without altering acute nociceptive responses. This effect is centrally controlled, as activity in hunger-sensitive agoutirelated protein (AgRP)-expressing neurons abrogates inflammatory pain. Systematic analysis of AgRP projection subpopulations revealed that the neural processing of hunger and inflammatory pain converge in the hindbrain parabrachial nucleus (PBN). Strikingly, activity in AgRP -> PBN neurons blocked the behavioral response to inflammatory pain as effectively as hunger or analgesics. The anti-nociceptive effect of hunger is mediated by neuropeptide Y(NPY) signaling in the PBN. By investigating the intersection between hunger and pain, we have identified a neural circuit that mediates competing survival needs and uncovered NPY Y1 receptor signaling in the PBN as a target for pain suppression.

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