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脊髓αB-晶体蛋白参与大鼠骨癌痛维持的证据。

Evidence of the involvement of spinal αB-crystallin in the maintenance of bone cancer pain in rats.

机构信息

Department of Anesthesiology, Kunshan First People's Hospital Affiliated to Jiangsu University, Kunshan, 215000, Jiangsu, People's Republic of China.

Department of Otorhinolaryngology, Xinhua Hospital Affiliated to Jiaotong University School of Medicine, Shanghai, 200092, People's Republic of China.

出版信息

Pharmacol Rep. 2020 Feb;72(1):208-213. doi: 10.1007/s43440-019-00052-7. Epub 2020 Jan 8.

Abstract

BACKGROUND

αB-crystallin (CRYAB) is a small heat shock protein that is able to inhibit neuroinflammatory responses under various pathological conditions. Some studies have proven that neuroinflammatory mechanisms play important roles in bone cancer pain (BCP). However, whether CRYAB participates in the maintenance of BCP has not yet been examined.

METHODS

Walker256 tumour cells were inoculated into the tibia to induce a rat model of BCP. Von Frey hairs were used to measure mechanical allodynia. Immunohistochemistry and western blotting were used to examine the expression level of CRYAB in the spinal dorsal horn.

RESULTS

The gradual development of mechanical allodynia was induced by the injection of Walker256 cells into the tibia. The downregulation of spinal CRYAB expression was found in BCP rats. The intrathecal administration of CRYAB (from days 9 to 15 post-inoculation) dose-dependently alleviated mechanical allodynia in BCP rats. Additionally, there were concomitant increases in spinal CRYAB expression and decreases in TNF-α expression.

CONCLUSIONS

Spinal CRYAB may participate in the maintenance of BCP in rats. The findings will help to identify new drugs for the management of BCP.

摘要

背景

αB-晶状体蛋白(CRYAB)是一种小热休克蛋白,能够在各种病理条件下抑制神经炎症反应。一些研究已经证明,神经炎症机制在骨癌痛(BCP)中发挥重要作用。然而,CRYAB 是否参与 BCP 的维持尚未得到检验。

方法

将 Walker256 肿瘤细胞接种到胫骨中,以诱导大鼠 BCP 模型。使用 Von Frey 毛发测量机械性痛觉过敏。免疫组织化学和 Western blot 用于检测脊髓背角中 CRYAB 的表达水平。

结果

向胫骨内注射 Walker256 细胞逐渐诱导出机械性痛觉过敏。BCP 大鼠脊髓 CRYAB 表达下调。鞘内给予 CRYAB(接种后第 9 至 15 天)剂量依赖性地缓解 BCP 大鼠的机械性痛觉过敏。此外,脊髓 CRYAB 表达增加,TNF-α 表达减少。

结论

脊髓 CRYAB 可能参与大鼠 BCP 的维持。这些发现将有助于确定用于管理 BCP 的新药。

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