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Nociceptor activation and protein extravasation induced by inflammatory mediators in human skin.

机译:人皮肤中炎症介质诱导的伤害感受器激活和蛋白质外渗。

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Protein extravasation (PE) is known to play an important role in inflammatory conditions. In this study we used dermal microdialysis to apply inflammatory mediators (histamine, bradykinin, serotonin) to human skin. Locally induced PE was compared to pain ratings and axon reflex erythema measured simultaneously. Linear microdialysis capillaries (outer diameter 0.4 mm; cut-off 3000 kDa) were inserted intracutaneously at a length of 1.5 cm in the volar forearm of healthy volunteers. The capillaries were perfused with Ringer's solution at a constant flow rate of 4 microl/min. The perfusate was sampled at 15-min intervals and was analysed for total protein concentration. After a baseline of 60 min, the perfusion was switched to inflammatory mediators for 30 min and then back to vehicle again. Sensations evoked by the stimulation were assessed on a visual analogue scale and visible axon reflex erythema was measured planimetrically.Dose-dependent increases in PE could be assessed for all inflammatory mediators tested. Bradykinin (10(-7)M) induced a significant PE, whereas serotonin was effective only at a concentration of 10(-3)M. While serotonin in lower concentrations induced moderate burning pain and an axon reflex flare but no PE, bradykinin provoked PE without pain or axon reflex flare at a concentration of 10(-7)M. Application of histamine similarly evoked PE at lower concentrations as compared to the induction of itch sensation and axon reflex flare.It is concluded that there is no link between nociceptor activation and protein extravasation induced by inflammatory mediators in healthy human skin. Copyright 2001 European Federation of Chapters of the International Association for the Study of Pain.
机译:众所周知,蛋白质外渗(PE)在炎症中起重要作用。在这项研究中,我们使用了皮肤微透析技术将炎症介质(组胺,缓激肽,血清素)应用于人体皮肤。将局部诱发的PE与同时评估的疼痛等级和轴突反射性红斑进行比较。将线性微透析毛细血管(外径0.4 mm;截断值3000 kDa)以1.5 cm的长度皮内插入健康志愿者的掌前臂中。毛细管以4微升/分钟的恒定流速灌注林格氏液。每隔15分钟取样一次灌注液,并分析总蛋白浓度。在基线60分钟后,将灌注切换至炎症介质30分钟,然后再次恢复至溶媒。刺激引起的感觉在视觉模拟量表上进行评估,并通过轴测法测量可见的轴突反射性红斑。可以评估所测试的所有炎性介质中PE的剂量依赖性增加。缓激肽(10(-7)M)引起明显的PE,而血清素仅在10(-3)M浓度下有效。较低浓度的5-羟色胺会引起中度烧灼痛和轴突反射性耀斑,但没有PE,缓激肽在浓度为10(-7)M时会引起PE疼痛或轴突反射性耀斑。与诱导瘙痒感和轴突反射耀斑相比,组胺的应用同样可以诱发较低的PE。结论:在健康的人皮肤中,伤害感受器激活与炎症介质诱导的蛋白质外渗之间没有联系。国际疼痛研究协会欧洲分会2001年版权所有。

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