Oxytocin ameliorates bone cancer pain by suppressing toll-like receptor 4 and proinflammatory cytokines in rat spinal cord.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Journal of neurogenetics Pub Date : 2020-03-01 Epub Date: 2020-03-02 DOI:10.1080/01677063.2019.1711077
Xiaping Mou, Ji Fang, An Yang, Gang Du
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引用次数: 11

Abstract

Bone cancer pain is considered to be mechanistically unique compared with inflammatory or neuropathic pain states. Toll-like receptor 4 (TLR4) is a transmembrane receptor protein which has been reported to be involved in neuropathic pain. However, the role of TLR4 in bone cancer pain is still unclear. Therefore, the aim of this study is to investigate the hypothesis that oxytocin may ameliorate bone cancer pain by suppressing TLR4 in spinal cord. Behavioral analysis and molecular biological experiments were carried out. Our data demonstrated that intrathecally delivery of oxytocin significantly ameliorated the mechanical allodynia and thermal hyperalgesia in bone cancer pain rats. Moreover, oxytocin suppressed the up-regulation of TLR4 and proinflammatory cytokines TNFα and IL-1β in spinal cord of bone cancer pain rats. Therefore, we concluded that intrathecal administration of oxytocin relieves bone cancer pain by suppressing the up-regulation of TLR4, TNFα and IL-1β in spinal cord. Oxytocin possesses analgesic efficacy against bone cancer pain and deserves further to confirm its effectiveness in clinically relevant of cancer pain.

催产素通过抑制大鼠脊髓toll样受体4和促炎细胞因子改善骨癌疼痛。
与炎性或神经性疼痛状态相比,骨癌疼痛被认为在机制上是独特的。toll样受体4 (TLR4)是一种跨膜受体蛋白,已被报道参与神经性疼痛。然而,TLR4在骨癌疼痛中的作用尚不清楚。因此,本研究的目的是探讨催产素可能通过抑制脊髓TLR4来改善骨癌疼痛的假设。进行行为分析和分子生物学实验。我们的数据表明,鞘内注入催产素可显著改善骨癌痛大鼠的机械异常性痛和热痛觉过敏。此外,催产素抑制了骨癌痛大鼠脊髓中TLR4和促炎因子TNFα、IL-1β的上调。因此,我们认为鞘内注射催产素通过抑制脊髓中TLR4、TNFα和IL-1β的上调来缓解骨癌疼痛。催产素对骨癌性疼痛具有镇痛作用,其在癌痛相关临床中的有效性有待进一步证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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