首页> 外文期刊>European journal of pain : >The neurokinin-1 receptor antagonist RP 67580 reduces the sensitization of primary afferents by substance P in the rat.
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The neurokinin-1 receptor antagonist RP 67580 reduces the sensitization of primary afferents by substance P in the rat.

机译:神经激肽-1受体拮抗剂RP 67580降低了大鼠中P物质对原发传入神经的敏感性。

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摘要

The inflammatory mediator substance P (SP) produces a variety of biological effects in several tissues by binding to the tachykinin receptor neurokinin 1 (NK1) and, to a lesser extent, by binding to the neurokinin 2 receptor (NK2). To assess the sensitizing effect of SP on articular afferent fibres the NK1receptor antagonist RP 67580 was applied in normal and acutely inflamed rat knee joints.Altogether 38 fine afferent nerve fibres from the rat knee with conduction velocities of 0.71-13.5 m/s were recorded as single units, during non-noxious and noxious joint rotations. SP, injected i.a. as a bolus close to the knee joint, was able to sensitize 45.5% (10 of 22) of the units recorded from normal joints and 33.3% (five of 15) of afferents from inflamed joints. The following i.a. application of RP 67580 in a range of 20-200 nmol antagonized in a dose-dependent manner the sensitizing effect of SP in a large proportion of slowly conducting articular afferents from normal (66.7%) and inflamed (46.2%) knee joints. Subsequent SP application enhanced the afferent sensitivity further. The electrophysiological results presented here further support the suggestion that the sensitization of afferents by SP in the rat knee joint is mediated mainly by the NK1 receptor, which is probably located on the primary afferents. Copyright 2001 European Federation of Chapters of the International Association for the Study of Pain.
机译:炎症介质P(SP)通过与速激肽受体神经激肽1(NK1)结合,并在较小程度上通过与神经激肽2受体(NK2)结合,在多种组织中产生多种生物学作用。为了评估SP对关节传入纤维的敏化作用,将NK1受体拮抗剂RP 67580用于正常和急性发炎的大鼠膝关节。记录总共38条来自大鼠膝盖的传入神经纤维,传导速度为0.71-13.5 m / s,记录为非有害和有害联合旋转中的单个单位。 SP,注射i.a.作为靠近膝关节的推注,能够敏化从正常关节记录的单位的45.5%(22个中的10个)和从发炎的关节中传入的33.3%(15个中的五个)。以下i.a. RP 67580在20-200 nmol范围内的剂量依赖性拮抗SP对大部分正常(66.7%)和发炎(46.2%)膝关节的缓慢传导关节传入的SP的敏化作用。随后的SP应用进一步提高了传入灵敏度。此处提出的电生理结果进一步支持了这样的建议,即大鼠膝关节中SP传入的敏化作用主要是由NK1受体介导的,而NK1受体可能位于初级传入上。国际疼痛研究协会欧洲分会2001年版权所有。

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