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三氟淫羊藿素通过α7烟碱型乙酰胆碱受体介导的BDNF/TrkB/KCC2信号通路的阻断抑制小胶质细胞激活,从而改善 spared神经损伤诱导的大鼠脊髓神经性疼痛。 (注:这里“spared nerve injury”原文可能有误,推测是“spared nerve injury”应是“spared nerve injury”,即“保留神经损伤” ,可根据实际情况调整。)

Trifluoro-icaritin ameliorates spared nerve injury-induced neuropathic pain by inhibiting microglial activation through α7nAChR-mediated blockade of BDNF/TrkB/KCC2 signaling in the spinal cord of rats.

作者信息

Jia Dandan, Liu Guangsen, Sun Yalan, Hu Zhiping, Huang Zhihua, Huang Cheng

机构信息

Department of Physiology, School of Basic Medicine Sciences, Gannan Medical University, Ganzhou 341000, PR China.

Pain Medicine Research Institute, Gannan Medical University, Ganzhou 341000, PR China.

出版信息

Biomed Pharmacother. 2023 Jan;157:114001. doi: 10.1016/j.biopha.2022.114001. Epub 2022 Nov 11.

Abstract

Neuropathic pain is still a serious and unsolved health problem. Activation of α7 nicotinic acetylcholine receptor (α7nAChR) is known to modulate neuropathic pain by inhibiting microglial activation and BDNF/TrkB/KCC2 signaling. We previously identified that trifluoro-icaritin (ICTF) has an attenuated effect on spared nerve injury (SNI)-induced neuropathic pain, but its potential mechanisms remain unknown. Here, the pain-related behaviors were determined by paw withdrawal threshold (PWT), CatWalk gait analysis, rotarod test, open field test and elevated plus maze test. The expression of pain-related signal molecules was evaluated by Western blot and immunofluorescence staining. The results showed that ICTF (5.0 mg/kg, i.p.) successfully relieved SNI-induced mechanical allodynia and anxiety-like behavior, we subsequently found there existed either positive or negative correlation between mechanical allodynia and gait parameters or rotating speed following ICTF treatment. Moreover, ICTF not only enhanced the expression of spinal α7nAChR, KCC2, CD206 and IL-10, but also decreased the levels of spinal BDNF, TrkB, CD11b, Iba-1, CD40 and IL-1β in SNI rats. Conversely, α7nAChR antagonist α-Bgtx (I.T.) effectively reversed the inhibitory effects of ICTF on SNI rats, resulting in a remarkable improvement of mechanical allodynia, activation of microglia. and suppression of α7nAChR-mediated BDNF/TrkB/KCC2 signaling. Additionally, exogenous BDNF (I.T.) dramatically abrogated both blockade of BDNF/TrkB/KCC2 cascade and alleviation of mechanical allodynia by ICTF treatment. Altogether, the study highlighted that ICTF could relieve SNI-induced neuropathic pain by suppressing microglial activation via α7nAChR-mediated inhibition of BDNF/TrkB/KCC2 signaling in the spinal cord, suggesting that ICTF may be served as a possible painkiller against neuropathic pain.

摘要

神经性疼痛仍然是一个严重且尚未解决的健康问题。已知激活α7烟碱型乙酰胆碱受体(α7nAChR)可通过抑制小胶质细胞激活和BDNF/TrkB/KCC2信号传导来调节神经性疼痛。我们之前发现三氟淫羊藿素(ICTF)对 spared nerve injury(SNI)诱导的神经性疼痛具有减轻作用,但其潜在机制仍不清楚。在此,通过 paw withdrawal threshold(PWT)、CatWalk步态分析、转棒试验、旷场试验和高架十字迷宫试验来确定疼痛相关行为。通过蛋白质免疫印迹和免疫荧光染色评估疼痛相关信号分子的表达。结果表明,ICTF(5.0mg/kg,腹腔注射)成功缓解了SNI诱导的机械性异常性疼痛和焦虑样行为,随后我们发现ICTF治疗后机械性异常性疼痛与步态参数或旋转速度之间存在正相关或负相关。此外,ICTF不仅增强了脊髓α7nAChR、KCC2、CD206和IL-10的表达,还降低了SNI大鼠脊髓中BDNF、TrkB、CD11b、Iba-1、CD40和IL-1β的水平。相反,α7nAChR拮抗剂α-Bgtx(鞘内注射)有效地逆转了ICTF对SNI大鼠的抑制作用,导致机械性异常性疼痛显著改善、小胶质细胞激活以及α7nAChR介导的BDNF/TrkB/KCC2信号传导受到抑制。此外,外源性BDNF(鞘内注射)显著消除了ICTF治疗对BDNF/TrkB/KCC2级联反应的阻断以及对机械性异常性疼痛的缓解。总之,该研究强调ICTF可通过α7nAChR介导的脊髓BDNF/TrkB/KCC2信号传导抑制来抑制小胶质细胞激活,从而缓解SNI诱导的神经性疼痛,表明ICTF可能作为一种治疗神经性疼痛的潜在止痛药。

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