Suppr超能文献

白藜芦醇对 NF-κB 的抑制作用:实验性糖尿病神经病变神经保护的可能机制。

NF-kappaB inhibitory action of resveratrol: a probable mechanism of neuroprotection in experimental diabetic neuropathy.

机构信息

Molecular Neuropharmacology Laboratory, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Sector-67, S.A.S. Nagar, Punjab 160062, India.

出版信息

Biochem Biophys Res Commun. 2010 Apr 2;394(2):360-5. doi: 10.1016/j.bbrc.2010.03.014. Epub 2010 Mar 6.

Abstract

Resveratrol has shown array of biological actions, and is under clinical development for various disease conditions. The etiology of diabetic neuropathy revolves around oxidative stress, AGE formation, lipid peroxidation etc. All these stimulate inflammatory processes and NF-kappaB cascade is considered as one of the major players of inflammatory response. Activation of NF-kappaB results in elevated levels of inflammatory mediators. COX-2 and TNF-alpha activity have also been correlated with inflammatory damage in the pathophysiology of diabetic neuropathy (DN). Therefore we investigated the effect of resveratrol on NF-kappaB inflammatory cascade, COX-2, TNF-alpha and IL-6 levels in experimental DN. We found that resveratrol protected against various functional and behavioral deficits in diabetic neuropathy in line with our earlier published reports. In this study we found that the resveratrol treatment decreased the expression of p65 and IkappaB-alpha in treated rats. Treatment also ameliorated the elevated levels of TNF-alpha, IL-6 and COX-2. Resveratrol treatment produced significant decrease in nerve MDA levels in treated animals which may also be contributing to reduction in neuro-inflammation. This study confirms the NF-kappaB inhibitory activity and anti-inflammatory activity of resveratrol which may contribute to neuroprotection in diabetic neuropathy apart from its antioxidant effect.

摘要

白藜芦醇具有多种生物学作用,目前正在临床开发用于治疗各种疾病。糖尿病神经病变的病因围绕氧化应激、AGE 形成、脂质过氧化等。所有这些都会刺激炎症过程,NF-κB 级联反应被认为是炎症反应的主要参与者之一。NF-κB 的激活导致炎症介质水平升高。COX-2 和 TNF-α的活性也与糖尿病神经病变(DN)的病理生理学中的炎症损伤相关。因此,我们研究了白藜芦醇对实验性糖尿病神经病变中 NF-κB 炎症级联、COX-2、TNF-α和 IL-6 水平的影响。我们发现,白藜芦醇可预防糖尿病神经病变的各种功能和行为缺陷,这与我们之前发表的报告一致。在这项研究中,我们发现白藜芦醇治疗可降低治疗大鼠中 p65 和 IkappaB-α的表达。治疗还可改善 TNF-α、IL-6 和 COX-2 的升高水平。白藜芦醇治疗可显著降低治疗动物的神经 MDA 水平,这也可能有助于减少神经炎症。这项研究证实了白藜芦醇的 NF-κB 抑制活性和抗炎活性,除了其抗氧化作用外,还可能有助于糖尿病神经病变的神经保护。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验