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腹腔给予 Met-RANTES 可减轻小鼠神经病理性疼痛模型中的炎症和痛觉反应。

Peritoneal administration of Met-RANTES attenuates inflammatory and nociceptive responses in a murine neuropathic pain model.

机构信息

Department of Anesthesiology, Transgenic & Molecular Immunogenetics Laboratory, Chang Gung Memorial Hospital, Linkou,Taiwan, ROC.

出版信息

J Pain. 2013 Jan;14(1):24-35. doi: 10.1016/j.jpain.2012.09.015. Epub 2012 Nov 23.

DOI:10.1016/j.jpain.2012.09.015
PMID:23183003
Abstract

UNLABELLED

The C-C motif chemokine ligand 5 (CCL5; also known as regulated on activation, normal T expressed and secreted, or RANTES) is a member of the CC family of chemokines that specifically attract and activate leukocytes to sites of inflammation. Although CCL5 has been implicated in the processing of pain, its detailed mechanisms of action are still unknown. In this study, we investigated the potential of the Met-RANTES, a selective CCL5 receptor antagonist, via peritoneal administration to modulate the recruitment of inflammatory cells in injured sites and attenuate nociceptive responses in a neuropathic pain model in mice. Nociceptive sensitization, immune cell infiltration, multiple cytokine secretion, and opioid peptide expression in damaged nerves were studied. Our results indicated that Met-RANTES-treated mice had less behavioral hypersensitivity after partial sciatic nerve ligation. Macrophage infiltration, pro-inflammatory cytokine (TNFα, IL-1β, IL-6, and IFNγ) protein secretion, and enkephalin, β-endorphin, and dynorphin mRNA expression in damaged nerves following partial sciatic nerve ligation were significantly decreased, and anti-inflammatory cytokine (IL-10) protein was significantly increased in Met-RANTES-treated mice. These results suggest that CCL5 is capable of regulating the microenvironment that controls behavioral hypersensitivity at the level of the peripheral injured site in a murine chronic neuropathic pain model.

PERSPECTIVE

The present study identifies the potent pro-inflammatory potential of CCL5 and verifies the possible role of selective CCL5 receptor inhibitor in a murine neuropathic pain model.

摘要

未标记

C-C 基序趋化因子配体 5(CCL5;也称为活化调节正常 T 细胞表达和分泌,或 RANTES)是趋化因子 CC 家族的成员,其特异性吸引并激活白细胞到炎症部位。尽管 CCL5 与疼痛处理有关,但其详细的作用机制尚不清楚。在这项研究中,我们通过腹腔给药研究了选择性 CCL5 受体拮抗剂 Met-RANTES 的潜力,以调节损伤部位炎症细胞的募集,并减轻小鼠神经病理性疼痛模型中的伤害性反应。研究了伤害性感受敏化、免疫细胞浸润、多种细胞因子分泌和损伤神经中的阿片肽表达。我们的结果表明,在部分坐骨神经结扎后,给予 Met-RANTES 的小鼠行为敏感性较低。巨噬细胞浸润、促炎细胞因子(TNFα、IL-1β、IL-6 和 IFNγ)蛋白分泌以及损伤神经中脑啡肽、β-内啡肽和强啡肽 mRNA 表达在部分坐骨神经结扎后明显减少,而抗炎细胞因子(IL-10)蛋白在 Met-RANTES 治疗的小鼠中明显增加。这些结果表明,CCL5 能够调节小鼠慢性神经病理性疼痛模型中损伤部位外周水平控制行为敏感性的微环境。

观点

本研究确定了 CCL5 的强烈促炎潜力,并验证了选择性 CCL5 受体抑制剂在小鼠神经病理性疼痛模型中的可能作用。

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