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虾青素对大鼠脊髓损伤模型的抗炎和抗氧化作用。

Anti-inflammatory and antioxidant effects of astaxanthin following spinal cord injury in a rat animal model.

机构信息

Department of Pharmacology, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.

Neurobiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Brain Res Bull. 2021 Dec;177:324-331. doi: 10.1016/j.brainresbull.2021.10.014. Epub 2021 Oct 22.

Abstract

Spinal cord injury (SCI) is a severely debilitating problem leading to substantial decrease in the quality of life. After spinal cord injury, inflammation and oxidative stress plays a key role in initiating the secondary injury cascades leading to progressive tissue degradation and extreme functional deficits. Given that the primary mechanical injuries to spinal cord are rarely repaired, the pharmacological interventions may improve the neurological outcomes caused by secondary injury. Astaxanthin (AST) is considered as a xanthophyll carotenoid with potent antioxidant and anti-inflammatory properties, which has various pharmacological activities. In the present study, we aimed to firstly assess the protective effect of AST, and then to define the AST mechanism of action on a rat model of SCI. Based on the results of von Frey test, AST treatment significantly alleviated the SCI-induced neuropathic pain compared with the control groups (P < 0.05). The expression analysis by western blot shows reduced expression levels of COX-2, TNF-α, IL-1β, and IL-6 following AST treatment (P < 0.05). The activity of antioxidant enzymes was evaluated using ELISA. Therefore, ELISA experiments showed a significant reduction in the level of oxidative stress in SCI rat following AST treatment (P < 0.05). Furthermore, histopathological evaluations revealed that myelinated white matter and motor neuron number were significantly preserved after treatment with AST (P < 0.05). In conclusion, our study shows that AST could improve SCI through anti-inflammatory and antioxidant effects which leads to decreased tissue damage and mechanical pain after SCI.

摘要

脊髓损伤(SCI)是一个严重的致残问题,导致生活质量大幅下降。脊髓损伤后,炎症和氧化应激在启动继发性损伤级联反应中起着关键作用,导致进行性组织退化和严重的功能缺陷。鉴于脊髓的主要机械损伤很少得到修复,药物干预可能会改善继发性损伤引起的神经功能预后。虾青素(AST)被认为是一种具有强大抗氧化和抗炎特性的叶黄素类胡萝卜素,具有多种药理活性。在本研究中,我们旨在首先评估 AST 的保护作用,然后确定 AST 在 SCI 大鼠模型中的作用机制。基于von Frey 测试的结果,AST 治疗组与对照组相比,SCI 诱导的神经性疼痛明显减轻(P<0.05)。Western blot 表达分析显示,AST 治疗后 COX-2、TNF-α、IL-1β 和 IL-6 的表达水平降低(P<0.05)。采用 ELISA 评估抗氧化酶的活性。因此,ELISA 实验显示,AST 治疗后 SCI 大鼠的氧化应激水平显著降低(P<0.05)。此外,组织病理学评估显示,AST 治疗后髓鞘白质和运动神经元数量明显保存(P<0.05)。总之,我们的研究表明,AST 通过抗炎和抗氧化作用改善 SCI,从而减少 SCI 后的组织损伤和机械性疼痛。

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