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解析 D3 促进脊髓损伤后的炎症消退、神经保护和功能恢复。

Resolvin D3 Promotes Inflammatory Resolution, Neuroprotection, and Functional Recovery After Spinal Cord Injury.

机构信息

Department of Neurosurgery, CHA University School of Medicine, CHA Bundang Medical Center, Seongnam-si, Gyeonggi-do, 13496, Republic of Korea.

Department of Biomedical Science, CHA University School of Medicine, Seongnam-si, Gyeonggi-do, Republic of Korea.

出版信息

Mol Neurobiol. 2021 Jan;58(1):424-438. doi: 10.1007/s12035-020-02118-7. Epub 2020 Sep 22.

Abstract

Resolvins, a new family from the endogenous specialized pro-resolving mediators (SPMs), promote the resolution of the inflammatory response. Resolvin D3 (RvD3), a docosahexaenoic acid (DHA) product, has been known to suppress the inflammatory response. However, the anti-inflammatory and neuroprotective effects of RvD3 are not known in a model of spinal cord injury (SCI). Here, we investigated the anti-inflammatory and neuroprotective effect of RvD3 in a mouse model of SCI. Processes associated with anti-inflammation and angiogenesis were studied in RAW 264.7 cells and the human brain endothelial cell line hCMEC/D3, respectively. Additionally, female C57BL/6 mice were subjected to moderate compression SCI (20-g weight compression for 1 min) followed by intrathecal injection of vehicle or RvD3 (1 μg/20 μL) at 1 h post-SCI. RvD3 decreased the lipopolysaccharide (LPS)-induced production of inflammatory mediators and nitric oxide (NO) in RAW 264.7 cells and promoted an angiogenic effect in the hCMEC/D3 cell line. Treatment with RvD3 improved locomotor recovery and reduced thermal hyperalgesia in SCI mice compared with vehicle treatment at 14 days post-SCI. Remarkably, RvD3-treated mice exhibited reduced expression of inflammatory cytokines (TNF-α, IL6, IL1β) and chemokines (CCL2, CCL3). Also, RvD3-treated mice exhibited increased expression of tight junction proteins such as zonula occludens (ZO)-1 and occludin. Furthermore, immunohistochemistry showed a decreased level of gliosis (GFAP, Iba-1) and neuroinflammation (CD68, TGF-β) and enhanced neuroprotection. These data provide evidence that intrathecal injection of RvD3 represents a promising therapeutic strategy to promote inflammatory resolution, neuroprotection, and neurological functional recovery following SCI.

摘要

解析素是内源性特异性促解决介质(SPM)的一个新家族,可促进炎症反应的解决。二十二碳六烯酸(DHA)产物解析素 D3(RvD3)已被证实可抑制炎症反应。然而,在脊髓损伤(SCI)模型中,RvD3 的抗炎和神经保护作用尚不清楚。在这里,我们研究了 RvD3 在 SCI 小鼠模型中的抗炎和神经保护作用。在 RAW 264.7 细胞和人脑血管内皮细胞系 hCMEC/D3 中分别研究了与抗炎和血管生成相关的过程。此外,雌性 C57BL/6 小鼠接受中度压迫性 SCI(20-g 重量压迫 1 分钟),然后在 SCI 后 1 小时通过鞘内注射载体或 RvD3(1μg/20μL)。RvD3 降低了脂多糖(LPS)诱导的 RAW 264.7 细胞中炎症介质和一氧化氮(NO)的产生,并在 hCMEC/D3 细胞系中促进了血管生成作用。与载体处理相比,RvD3 治疗在 SCI 后 14 天改善了运动功能恢复并减轻了热痛觉过敏。值得注意的是,RvD3 处理的小鼠表现出炎症细胞因子(TNF-α、IL6、IL1β)和趋化因子(CCL2、CCL3)表达减少。此外,RvD3 处理的小鼠表现出紧密连接蛋白(ZO-1 和闭合蛋白)表达增加。此外,免疫组织化学显示神经胶质增生(GFAP、Iba-1)和神经炎症(CD68、TGF-β)减少和神经保护增强。这些数据提供了证据,表明鞘内注射 RvD3 代表了一种有前途的治疗策略,可促进 SCI 后炎症解决、神经保护和神经功能恢复。

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