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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Time course and nerve growth factor dependence of inflammation-induced alterations in electrophysiological membrane properties in nociceptive primary afferent neurons.
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Time course and nerve growth factor dependence of inflammation-induced alterations in electrophysiological membrane properties in nociceptive primary afferent neurons.

机译:伤害性原发传入神经元中炎症诱导的电生理膜特性变化的时程和神经生长因子依赖性。

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摘要

Novel findings of changes in nociceptive dorsal root ganglion (DRG) neurons during hindlimb inflammation induced by complete Freund's adjuvant (CFA) injections in the hindpaw and hindleg are reported. These include increased maximum fiber following frequency in nociceptive C- and Adelta-fiber units by 2.7 and 3 times, respectively, and increased incidence of ongoing (spontaneous) activity by 3.3 times (to 54%) and 2.4 times (to 27%), respectively. These changes and the CFA-induced changes in somatic action potential (AP) configuration in nociceptive neurons (Djouhri and Lawson, 1999) were incomplete 24 hr after CFA. The nerve growth factor (NGF) dependence of the inflammation-induced changes was examined by injecting a synthetic NGF sequestering protein [tyrosine receptor kinase A Ig2 (trkA Ig2)] with CFA and subsequently into the CFA injection sites. NGF sequestration prevented some CFA-induced changes in nociceptive neurons including: the increased fiber following frequency (C and Adelta), the increased proportions of units with ongoing activity (C and Adelta), the decreased AP duration (C and Adelta), but not the decreased afterhyperpolarization (AHP) durations (C, Adelta, and Aalpha/beta) (Djouhri and Lawson, 1999). AP variables of nociceptive units with spontaneous activity were examined. The time course of electrophysiological changes in nociceptive units is consistent with processes involving altered protein expression and/or retrograde transport of factors. These results (1) implicate NGF in regulating inflammation-induced decreases in AP duration and in increases in firing rate and spontaneous activity but not in decreases in AHP duration and (2) suggest clinical advantages of reducing NGF in some inflammatory pain states.
机译:据报道,在后足和后肢完全注射弗氏佐剂(CFA)后,后肢发炎期间,伤害性背根神经节(DRG)神经元发生变化,发现了新发现。其中包括伤害性C纤维和Adelta纤维单位的最大纤维跟随频率分别增加2.7和3倍,进行中(自发)活动的发生率增加3.3倍(至54%)和2.4倍(至27%),分别。这些变化和伤害性神经元中CFA诱导的体细胞动作电位(AP)构型变化(Djouhri和Lawson,1999)在CFA后24小时仍未完成。通过将合成的NGF螯合蛋白[酪氨酸受体激酶A Ig2(trkA Ig2)]与CFA注射在一起,然后将其注射到CFA注射部位,来检查炎症诱导的变化对神经生长因子(NGF)的依赖性。 NGF螯合阻止了CFA引起的伤害感受神经元的某些变化,包括:纤维跟随频率增加(C和Adelta),具有持续活动的单位比例增加(C和Adelta),AP持续时间减少(C和Adelta),但没有超极化(AHP)后持续时间(C,Adelta和Aalpha / beta)的下降(Djouhri和Lawson,1999年)。检查具有自发活动的伤害感受单元的AP变量。伤害感受单元的电生理变化的时间过程与涉及蛋白质表达改变和/或因子逆行转运的过程一致。这些结果(1)暗示NGF可以调节炎症诱导的AP持续时间的减少,并能提高放电率和自发活动,但不能降低AHP持续时间;(2)提示在某些炎症性疼痛状态下减少NGF的临床优势。

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