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Neonatal microglia come of age for inflammatory pain.

机译:新生儿小胶质细胞因炎症性疼痛而逐渐成熟。

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In this issue, you will find a paper by Vega-Avelaira et al. entitled 'Inflammation-induced hyperalgesia and spinal microglia reactivity in neonatal rat'. The central question addressed in this study is whether there is a relationship between spinal microglial activation and the increased pain sensitivity associated with cutaneous inflammation in neonatal rodents. Unlike peripheral inflammation, it well established that neuropathic pain is never observed in neonates. Consistent with this is the observation that in animal models of peripheral neuropathy, hypersensitivity to mechanical stimuli is absent if the injury is generated before the fourth post-natal week (Howard et al., 2005; Rule and Eisenach, 2006). A likely factor in the disparity between the behavioural outcomes to nerve injury in neonates and adults is the response of microglia to injury.
机译:在本期中,您将找到Vega-Avelaira等人的论文。题为“新生大鼠炎症诱导的痛觉过敏和脊髓小胶质细胞反应性”。在这项研究中解决的中心问题是,在新生啮齿类动物中,脊髓小胶质细胞活化与皮肤炎症相关的疼痛敏感性增加之间是否存在关系。与周围炎症不同,它很好地证明了从未在新生儿中观察到神经性疼痛。与此一致的是,在周围神经病的动物模型中,如果在产后第四个星期之前产生损伤,则对机械刺激不存在超敏反应(Howard等人,2005; Rule and Eisenach,2006)。小胶质细胞对损伤的反应可能是新生儿和成人对神经损伤的行为结果之间差异的一个可能因素。

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