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

机译:通过竞争需求状态抑制疼痛的神经回路

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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.
机译:饥饿和痛苦是个人必须解决的两个竞争信号,以确保生存。然而,优先考虑相互矛盾的生存需求的神经过程似乎很差。我们发现饥饿衰减炎症疼痛的行为应对和情感性质,而不会改变急性伤害反应。这种效果是集中控制的,作为饥饿敏感刺蛋白(AGRP)的活性 - 表达神经元消除炎症疼痛。 AGRP投影群的系统分析显示,在后脑桥核(PBN)中,饥饿和炎性疼痛的神经处理会聚。令人惊讶的是,AGRP - &GT的活动; PBN神经元随着饥饿或镇痛药而有效地阻止了对炎症疼痛的行为应答。饥饿的抗伤害效果由PBN中的神经肽Y(NPY)信号介导。通过研究饥饿和疼痛之间的交叉口,我们已经确定了一种神经电路,该神经电路介导竞争生存需要,并在PBN中发现的NPY Y1受体信号传导作为疼痛抑制的靶标。

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