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首页> 外文期刊>Life sciences >The sensitization of peripheral C-fibers to lysophosphatidic acid in bone cancer pain.
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The sensitization of peripheral C-fibers to lysophosphatidic acid in bone cancer pain.

机译:骨癌疼痛中外周C纤维对溶血磷脂酸的敏感性。

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AIMS: Lysophosphatidic acid (LPA) is released from injured tissue and cancer cells and is involved in the induction of neuropathic pain. The present study explores whether LPA plays a role in the development of osteocarcinoma-induced pain. MAIN METHODS: The bone cancer model was established using the Walker 256 mammary gland carcinoma cell line, and cancer-related behavioral and physiological changes were observed using von Frey, X-ray and immunohistochemical methods. The role of LPA in the bone cancer model and related mechanisms were examined by using in vitro single fiber recording and western blot. KEY FINDINGS: Rats exhibited severe hyperalgesia 2weeks after the cancer cell implantation. Several changes were observed at this time point including: ipsilateral dorsal root ganglion (DRG) neurons were labeled by injured neurons marker ATF3; LPA(1) receptor expression in DRG neurons was increased; sural C-fibers were more sensitive to LPA stimuli, and this response could be blocked by LPA receptor and substance P receptor antagonists. SIGNIFICANCE: These data indicate that LPA is involved in the induction of bone cancer pain through mechanisms of peripheral C-fibers sensitization. LPA and its downstream molecules possibly are promising therapeutic targets for treatment of cancer pain.
机译:目的:溶血磷脂酸(LPA)从受伤的组织和癌细胞中释放出来,并参与神经性疼痛的诱导。本研究探讨了LPA是否在骨癌诱发的疼痛的发展中起作用。主要方法:使用Walker 256乳腺癌细胞系建立骨癌模型,并使用von Frey,X射线和免疫组织化学方法观察与癌症相关的行为和生理变化。 LPA在骨癌模型中的作用及相关机制通过体外单纤维记录和蛋白质印迹进行了研究。主要发现:癌细胞植入后2周,大鼠表现出严重的痛觉过敏。在这一时间点观察到了一些变化,包括:用受伤的神经元标记ATF3标记同侧背根神经节(DRG)神经元; LPA(1)受体在DRG神经元中的表达增加;腓肠C纤维对LPA刺激更为敏感,该反应可能被LPA受体和P物质受体拮抗剂所阻断。意义:这些数据表明,LPA通过外周C纤维致敏机制参与了骨癌疼痛的诱导。 LPA及其下游分子可能是有望治疗癌症疼痛的治疗靶标。

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