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(-)-表没食子儿茶素没食子酸酯的抗痛觉过敏作用与脊髓中 CX3CL1 趋化因子表达减少有关。

(-)-Epigallocatechin-3-Gallate Antihyperalgesic Effect Associates With Reduced CX3CL1 Chemokine Expression in Spinal Cord.

机构信息

Research Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, Universitat de Girona, Girona, Spain.

Department of Physical Therapy, EUSES - Universitat de Girona, Girona, Spain.

出版信息

Phytother Res. 2017 Feb;31(2):340-344. doi: 10.1002/ptr.5753. Epub 2016 Nov 29.

DOI:10.1002/ptr.5753
PMID:27896922
Abstract

(-)-Epigallocatechin-3-gallate (EGCG) is a major polyphenol in green tea with beneficial effects on the neuropathic pain alleviation in animal models. Because chemokine fractalkine (CX3CL1) has been suggested as an important signal during neuropathic pain development, this study aimed to investigate whether CX3CL1 expression may be modulated by EGCG treatment reducing hyperalgesia in chronic constriction injured mice. To this end, Balb/c mice were subjected to a chronic constriction injury of sciatic nerve (CCI) and treated with EGCG or vehicle once a day during the first week following surgery. Thermal hyperalgesia was tested at 7 and 14 days post-surgery, and the expression of CX3CL1 and its mRNA were analyzed in spinal cord at the end of the experimental period. Results revealed that EGCG treatment significantly reduced thermal hyperalgesia in CCI-injured mice at short time, and this antihyperalgesic effect was associated with a down-regulation of CX3CL1 protein expression in the spinal cord. On the other hand, EGCG treatment did not affect the CX3CL1 transcription. Overall, our results suggest a new role of EGCG-treatment in an experimental model of neuropathic pain as a mediator of nociceptive signaling cross talk between neurons and glial cells in the dorsal horn of the spinal cord. Copyright © 2016 John Wiley & Sons, Ltd.

摘要

(-)-表没食子儿茶素没食子酸酯(EGCG)是绿茶中的一种主要多酚,对动物模型中的神经病理性疼痛缓解有有益作用。由于趋化因子 fractalkine(CX3CL1)已被认为是神经病理性疼痛发展过程中的重要信号,因此本研究旨在探讨 EGCG 治疗是否可能通过调节 CX3CL1 表达来减轻慢性缩窄性损伤小鼠的痛觉过敏。为此,Balb/c 小鼠接受坐骨神经慢性缩窄性损伤(CCI),并在手术后的第一周每天接受 EGCG 或载体治疗。术后 7 和 14 天测试热痛觉过敏,实验结束时分析脊髓中 CX3CL1 及其 mRNA 的表达。结果表明,EGCG 治疗可显著减轻 CCI 损伤小鼠的短期热痛觉过敏,这种抗痛觉过敏作用与脊髓中 CX3CL1 蛋白表达下调有关。另一方面,EGCG 治疗并不影响 CX3CL1 的转录。总体而言,我们的研究结果表明,EGCG 治疗在神经病理性疼痛的实验模型中具有新的作用,作为背角神经元和神经胶质细胞之间伤害性信号串扰的介体。版权所有 © 2016 年 John Wiley & Sons, Ltd.

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