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白细胞介素-1β在关节炎性疼痛中的作用:主要参与大鼠抗原诱导性关节炎的热痛觉过敏,而非机械性痛觉过敏。

The role of interleukin-1β in arthritic pain: main involvement in thermal, but not mechanical, hyperalgesia in rat antigen-induced arthritis.

作者信息

Ebbinghaus Matthias, Uhlig Benjamin, Richter Frank, von Banchet Gisela Segond, Gajda Mieczyslaw, Bräuer Rolf, Schaible Hans-Georg

机构信息

Jena University Hospital-Friedrich Schiller University of Jena, Jena, Germany.

出版信息

Arthritis Rheum. 2012 Dec;64(12):3897-907. doi: 10.1002/art.34675.

Abstract

OBJECTIVE

Interleukin-1β (IL-1β) is considered a pronociceptive cytokine, but its role in the generation of arthritic pain is unknown. The aim of this study was to investigate the role of IL-1β in arthritic pain and to explore the antinociceptive potential of the IL-1 receptor type I (IL-1RI) antagonist anakinra.

METHODS

Antigen-induced arthritis (AIA) was induced in rats. Expression of IL-1RI in the dorsal root ganglia (DRGs) was determined, and the effects of anakinra on inflammation, pain-related behavior, and receptor expression were assessed. In cultured DRG neurons, the effect of IL-1β on the expression of the transient receptor potential vanilloid 1 (TRPV-1) ion channel was examined. Recordings of action potentials from joint nociceptors were made after intraarticular injection of IL-1β into the rat knee joints.

RESULTS

AIA generated pronounced and persistent mechanical and thermal hyperalgesia, and IL-1RI expression in the lumbar DRGs was significantly up-regulated. Treatment with anakinra did not significantly reduce the severity of arthritis or mechanical hyperalgesia, but did result in a pronounced reduction in thermal hyperalgesia. In cultured DRG neurons, IL-1β up-regulated the expression of TRPV-1, a major transduction molecule involved in thermal hyperalgesia. During AIA, anakinra treatment down-regulated the expression of TRPV-1, consistent with the pronounced reduction in thermal hyperalgesia. IL-1β increased the mechanosensitivity of C-fibers of the joint, but reduced the mechanosensitivity of Aδ-fibers, thus having opposite effects on these mechanonociceptive nerve fibers.

CONCLUSION

In the context of arthritic knee pain, IL-1β and IL-1 receptors appear to be involved in thermal, rather than mechanical, hyperalgesia. Therefore, neutralization of IL-1β may be mainly antinociceptive in disease states characterized by thermal hyperalgesia, but not in disease states mainly characterized by mechanical hyperalgesia.

摘要

目的

白细胞介素-1β(IL-1β)被认为是一种促痛性细胞因子,但其在关节炎性疼痛产生中的作用尚不清楚。本研究的目的是探讨IL-1β在关节炎性疼痛中的作用,并探索I型白细胞介素-1受体(IL-1RI)拮抗剂阿那白滞素的镇痛潜力。

方法

在大鼠中诱导抗原诱导性关节炎(AIA)。测定背根神经节(DRG)中IL-1RI的表达,并评估阿那白滞素对炎症、疼痛相关行为和受体表达的影响。在培养的DRG神经元中,检测IL-1β对瞬时受体电位香草酸亚型1(TRPV-1)离子通道表达的影响。向大鼠膝关节内注射IL-1β后,记录关节伤害感受器的动作电位。

结果

AIA产生明显且持续的机械性和热性痛觉过敏,并且腰段DRG中IL-1RI的表达显著上调。用阿那白滞素治疗并没有显著降低关节炎的严重程度或机械性痛觉过敏,但确实导致热性痛觉过敏明显减轻。在培养的DRG神经元中,IL-1β上调TRPV-1的表达,TRPV-1是参与热性痛觉过敏的主要转导分子。在AIA期间,阿那白滞素治疗下调TRPV-1的表达,这与热性痛觉过敏的明显减轻一致。IL-1β增加关节C纤维的机械敏感性,但降低Aδ纤维的机械敏感性,因此对这些机械性伤害感受神经纤维有相反的作用。

结论

在膝关节炎性疼痛的背景下,IL-1β和IL-1受体似乎参与热性而非机械性痛觉过敏。因此,在以热性痛觉过敏为特征的疾病状态下,中和IL-1β可能主要具有镇痛作用,但在主要以机械性痛觉过敏为特征的疾病状态下则不然。

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