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Sustained sensitization and recruitment of rat cutaneous nociceptors by bradykinin and a novel theory of its excitatory action

机译:缓激肽对大鼠皮肤伤害感受器的持续增敏和募集及其兴奋作用的新理论

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摘要

class="enumerated" style="list-style-type:decimal">Excitation and sensitization to heat of nociceptors by bradykinin (BK) were examined using an isolated rat skin-saphenous nerve preparation.A total of 52 C-fibres was tested: 42 were mechano-heat sensitive (CMH) and 40 % of them were excited and sensitized to heat by BK superfusion (10−5m, 5 min) of their receptive fields; heat responses were augmented by more than five times and heat thresholds dropped to 36.4 °C, on average.Sixty per cent of the CMH did not respond to BK itself, but 3/4 of these units showed an increase in their heat responses by more than 100 % following BK exposure.Ten high-threshold mechanosensitive C-fibres did not discharge upon BK application but following this five of them responded to heat in a well-graded manner.In all fibres, the sensitizing effect of BK was abolished within 9 min or less of wash-out, and it could be reproduced several times at equal magnitude, whereas the excitatory effect of BK regularly showed profound tachyphylaxis.Sustained superfusion (20 min) of BK induced a desensitizing excitatory response while superimposed heat responses showed constant degrees of sensitization.The large extent and high prevalence of BK-induced sensitization (almost 80 % of all fibres tested) and de novo recruitment of heat sensitivity suggest a prominent role of BK not only in hyperalgesia but also in sustained inflammatory pain which may be driven by body or even lower local temperatures acting on sensitized nociceptors.Based on the latter assumption, a hypothesis is put forward that excludes a direct excitatory effect of BK on nociceptors, but assumes a temperature-controlled activation as a result of rapid and profound sensitization.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 用分离的大鼠皮肤隐神经制剂检查了缓激肽(BK)对伤害感受器的刺激和热敏感性。 总共测试了52种C纤维:42种对机械热敏感(CMH) BK的融合(10 −5 m,5分钟)使其中的40%受到刺激并对热敏感;热响应提高了五倍以上,平均热阈值降至36.4°C。 60%的CMH对BK本身没有响应,但是其中3/4的CMH显示BK暴露后,它们的热响应增加了100%以上。 十种高阈值机械敏感性C纤维在应用BK时并未释放,但在这五种之后,它们中的五种对热量的响应均达到了良好的等级 在所有纤维中,BK的敏化作用在洗脱后9分钟或更短时间内就消失了,并且可以等量复制多次,而BK的兴奋作用通常表现出极强的速激肽抑制作用 持续的BK灌注(20分钟)引起脱敏的兴奋性反应,而叠加的热反应则显示出恒定的致敏度。 BK引起的致敏作用的程度和发生率很高(几乎所有纤维的80%)和从头开始收集热敏性提示BK不仅在痛觉过敏中,而且在持续炎症性疼痛中起着重要的作用,这种炎症性疼痛可能是由机体甚至更低的局部温度作用于敏化伤害感受器所驱动。 基于后一种假设,提出了一个假设排除了BK对伤害感受器的直接兴奋作用,但由于迅速而深刻的敏化作用而假定了温度控制的激活作用。

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