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西红花酸可减轻小鼠坐骨神经分支选择性损伤诱导的神经性疼痛。

Crocetin attenuates spared nerve injury-induced neuropathic pain in mice.

作者信息

Wang Xiaolei, Zhang Guangqing, Qiao Yong, Feng Chang, Zhao Xin

机构信息

Department of Anesthesiology, The Second Hospital of Shandong University, 247 Bei Yuan Street, Jinan 250033, China.

ICU of LinYi Central Hospital, LinYi 276400, Shandong, China.

出版信息

J Pharmacol Sci. 2017 Dec;135(4):141-147. doi: 10.1016/j.jphs.2017.08.007. Epub 2017 Nov 24.

DOI:10.1016/j.jphs.2017.08.007
PMID:29217355
Abstract

Crocetin is the main component of saffron and exhibits anti-oxidative and anti-inflammatory effects. Neuroinflammation and oxidative stress have been recognized to play a crucial role in the pathogenesis of neuropathic pain. We investigated the effect of crocetin in a mouse model with neuropathic pain induced by spared nerve injury (SNI). Crocetin was intrathecally perfused at various doses for up to 12 days starting 3 days before the surgery. Behavioral tests were performed to determine pain sensitivity. The concentrations of proinflammatory cytokines tumor necrosis factor (TNF-α) and interleukin-1β (IL-1β) were measured to assess neuroinflammation. In addition, the enzymatic activity of superoxide dismutase (SOD) was measured to reveal the oxidative stress level. We found that repeated treatment with crocetin dose-dependently attenuated mechanical and thermal allodynia in SNI mice. In addition, treatment with high dose of crocetin reduced SNI-induced increase of TNF-α and IL-1β. Crocetin also restored the activity of mitochondrial MnSOD which was reduced in the sciatic nerve and the spinal cord of SNI mice. Collectively, our data demonstrate that crocetin effectively attenuates the neuropathic pain and significantly suppresses oxidative stress and neuroinflammation in the SNI mouse model, supporting the potential of crocetin in the treatment against neuropathic pain.

摘要

藏红花素是藏红花的主要成分,具有抗氧化和抗炎作用。神经炎症和氧化应激在神经性疼痛的发病机制中起着关键作用。我们研究了藏红花素对 spared nerve injury(SNI)诱导的神经性疼痛小鼠模型的影响。在手术前 3 天开始,以不同剂量鞘内灌注藏红花素,持续 12 天。进行行为测试以确定疼痛敏感性。测量促炎细胞因子肿瘤坏死因子(TNF-α)和白细胞介素-1β(IL-1β)的浓度以评估神经炎症。此外,测量超氧化物歧化酶(SOD)的酶活性以揭示氧化应激水平。我们发现,藏红花素重复治疗可剂量依赖性地减轻 SNI 小鼠的机械性和热性异常性疼痛。此外,高剂量藏红花素治疗可降低 SNI 诱导的 TNF-α和 IL-1β升高。藏红花素还恢复了 SNI 小鼠坐骨神经和脊髓中线粒体 MnSOD 的活性,而该活性在 SNI 小鼠中降低。总体而言,我们的数据表明,藏红花素可有效减轻神经性疼痛,并显著抑制 SNI 小鼠模型中的氧化应激和神经炎症,支持藏红花素在治疗神经性疼痛方面的潜力。

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