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An Improved Model of Heat-Induced Hyperalgesia—Repetitive Phasic Heat Pain Causing Primary Hyperalgesia to Heat and Secondary Hyperalgesia to Pinprick and Light Touch

机译:一种热致痛觉过敏的改进模型-反复性阵发性热痛引起原发性痛觉过敏导致发热继发性痛觉过敏导致针刺和轻触

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摘要

This study tested a modified experimental model of heat-induced hyperalgesia, which improves the efficacy to induce primary and secondary hyperalgesia and the efficacy-to-safety ratio reducing the risk of tissue damage seen in other heat pain models. Quantitative sensory testing was done in eighteen healthy volunteers before and after repetitive heat pain stimuli (60 stimuli of 48°C for 6 s) to assess the impact of repetitive heat on somatosensory function in conditioned skin (primary hyperalgesia area) and in adjacent skin (secondary hyperalgesia area) as compared to an unconditioned mirror image control site. Additionally, areas of flare and secondary hyperalgesia were mapped, and time course of hyperalgesia determined. After repetitive heat pain conditioning we found significant primary hyperalgesia to heat, and primary and secondary hyperalgesia to pinprick and to light touch (dynamic mechanical allodynia). Acetaminophen (800 mg) reduced pain to heat or pinpricks only marginally by 11% and 8%, respectively (n.s.), and had no effect on heat hyperalgesia. In contrast, the areas of flare (−31%) and in particular of secondary hyperalgesia (−59%) as well as the magnitude of hyperalgesia (−59%) were significantly reduced (all p<0.001). Thus, repetitive heat pain induces significant peripheral sensitization (primary hyperalgesia to heat) and central sensitization (punctate hyperalgesia and dynamic mechanical allodynia). These findings are relevant to further studies using this model of experimental heat pain as it combines pronounced peripheral and central sensitization, which makes a convenient model for combined pharmacological testing of analgesia and anti-hyperalgesia mechanisms related to thermal and mechanical input.
机译:这项研究测试了一种热致痛觉过敏的改良实验模型,该模型可提高诱导原发性和继发性痛觉过敏的功效,其功效与安全性之比可降低在其他热痛模型中看到的组织损伤风险。在重复性热痛刺激(60刺激性48°C刺激6 s)之前和之后,对18名健康志愿者进行了定量感官测试,以评估重复性热对条件性皮肤(原发性痛觉过敏区域)和邻近皮肤中体感功能的影响(与无条件镜像控制部位相比)。另外,绘制了耀斑和继发性痛觉过敏区域,并确定了痛觉过敏的时程。经过反复的热痛调节后,我们发现明显的原发性热痛觉过敏对热,原发性和继发性痛觉过敏对针刺和轻触(动态机械性异常性疼痛)。对乙酰氨基酚(800毫克)分别仅轻微地减少了11%和8%的热痛或针刺痛(n.s.),并且对热痛觉过敏没有影响。相比之下,耀斑面积(-31%)尤其是继发性痛觉过敏的面积(-59%)以及痛觉过敏的程度(-59%)显着降低(所有p <0.001)。因此,反复的热痛会引起明显的外周过敏(对热的主要痛觉过敏)和中枢过敏(点状痛觉过敏和动态机械性异常性疼痛)。这些发现与使用这种实验性热痛模型的进一步研究有关,因为它结合了明显的外周和中枢敏化作用,为结合热和机械输入的止痛和抗痛觉过敏机理的组合药理学测试提供了方便的模型。

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