Grape seed-derived procyanidins decreases neuropathic pain and nerve regeneration by suppression of toll-like receptor 4-myeloid differentiation factor-88 signaling.

IF 2.8 3区 医学 Q2 NEUROSCIENCES
Li Hu, Erdan An, ZhiPeng Zhu, Ying Cai, Xiaoyan Ye, Hongmei Zhou, Hejia Ge
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引用次数: 0

Abstract

Background: Recent studies have shown that peripheral nerve regeneration process is closely related to neuropathic pain. Toll-like receptor 4 (TLR4) signaling was involved in different types of pain and nerve regeneration. TLR4 induced the recruitment of myeloid differentiation factor-88 adaptor protein (MyD88) and NF-κB-depended transcriptional process in sensory neurons and glial cells, which produced multiple cytokines and promoted the induction and persistence of pain. Our study aimed to investigate procyanidins's effect on pain and nerve regeneration via TLR4-Myd88 signaling. Methods: Spinal nerve ligation (SNL) model was established to measure the analgesic effect of procyanidins. Anatomical measurement of peripheral nerve regeneration was measured by microscopy and growth associated protein 43 (GAP43) staining. Western blotting and/or immunofluorescent staining were utilized to detect TLR4, myeloid differentiation factor-88 adaptor protein (MyD88), ionized calcium-binding adapter molecule 1 (IBA1) and nuclear factor kappa-B-p65 (NF-κB-p65) expression, as well as the activation of astrocyte and microglia. The antagonist of TLR4 (LPS-RS-Ultra, LRU) were intrathecally administrated to assess the behavioral effects of blocking TLR4 signaling on pain and nerve regeneration. Result: Procyanidins reduced mechanical allodynia, thermal hyperalgesia and significantly suppressed the number of nerve fibers regenerated and the degree of myelination in SNL model. Compared with sham group, TLR4, MyD88, IBA1 and phosphorylation of NF-κB-p65 were upregulated in SNL rats which were reversed by procyanidins administration. Additionally, procyanidins also suppressed activation of spinal astrocytes and glial cells. Conclusion: Suppression of TLR4-MyD88 signaling contributes to the alleviation of neuropathic pain and reduction of nerve regeneration by procyanidins.

葡萄籽提取的原花青素通过抑制 TLR4-Myd88 信号传导,减轻神经病理性疼痛并促进神经再生
背景:最近的研究表明,外周神经再生过程与神经病理性疼痛密切相关。Toll样受体4(TLR4)信号转导参与了不同类型的疼痛和神经再生。TLR4诱导髓系分化因子-88适配蛋白(MyD88)的募集,以及感觉神经元和神经胶质细胞中依赖于NF-κB的转录过程,从而产生多种细胞因子,促进疼痛的诱发和持续。我们的研究旨在探讨原花青素通过TLR4-Myd88信号转导对疼痛和神经再生的影响:方法:建立脊神经结扎(SNL)模型来测量原花青素的镇痛效果。通过显微镜和生长相关蛋白43(GAP43)染色对周围神经再生进行解剖学测量。免疫印迹和/或免疫荧光染色用于检测TLR4、髓样分化因子-88适配蛋白(MyD88)、离子化钙结合适配分子1(IBA1)和核因子卡巴-B-p65(NF-κB-p65)的表达以及星形胶质细胞和小胶质细胞的活化。结果:原花青素能减轻SNL模型的机械异感和热痛,显著抑制神经纤维再生数量和髓鞘化程度。与假组相比,原花青素能逆转SNL大鼠TLR4、MyD88、IBA1和NF-κB-p65磷酸化的上调。此外,原花青素还能抑制脊髓星形胶质细胞和神经胶质细胞的活化:结论:原花青素抑制 TLR4-MyD88 信号传导有助于减轻神经病理性疼痛和减少神经再生。
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来源期刊
Molecular Pain
Molecular Pain 医学-神经科学
CiteScore
5.60
自引率
3.00%
发文量
56
审稿时长
6-12 weeks
期刊介绍: Molecular Pain is a peer-reviewed, open access journal that considers manuscripts in pain research at the cellular, subcellular and molecular levels. Molecular Pain provides a forum for molecular pain scientists to communicate their research findings in a targeted manner to others in this important and growing field.
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