Suppr超能文献

功能失调的核纤层蛋白作为埃默里-德赖富斯肌营养不良症中氧化应激的介质。

Dysfunctional lamins as mediators of oxidative stress in Emery-Dreifuss muscular dystrophy.

作者信息

Niebroj-Dobosz Irena, Sokołowska Beata, Madej-Pilarczyk Agnieszka, Marchel Michał, Hausmanowa-Petrusewicz Irena

出版信息

Folia Neuropathol. 2017;55(3):193-198. doi: 10.5114/fn.2017.70483.

Abstract

Deficit of lamin A/C or emerin causes genetically transmitted Emery-Dreifuss muscular dystrophy (EDMD). As lamins are considered to be mediators of oxidative stress, the antioxidant/oxidant status was examined. The total oxidant/antioxidant status in serum was examined in 29 cases of Emery-Dreifuss muscular dystrophy. The study included 12 autosomal-dominant laminopathies (AD-EDMD), 17 X-linked emerinopathies (X-EDMD) and 20 age-matched normal subjects. Total oxidant status (TOS) was reduced in all cases, and the total antioxidant capacity (TAC) was found to be decreased in the majority of the patients (in 82.8%). A relationship between TOS level and disease progression was noted. No correlation between TOS/TAC level and cardiological or neurological parameters was detected. The results of the study indicate disturbances of redox balance in EDMD patients. Determination of TOS/TAC might help to assess the progress of the disease and the potential effectiveness of antioxidant therapy.

摘要

核纤层蛋白A/C或emerin缺乏会导致遗传性埃默里-德赖富斯肌营养不良症(EDMD)。由于核纤层蛋白被认为是氧化应激的介质,因此对抗氧化/氧化状态进行了检测。对29例埃默里-德赖富斯肌营养不良症患者的血清总氧化/抗氧化状态进行了检测。该研究包括12例常染色体显性核纤层蛋白病(AD-EDMD)、17例X连锁emerin病(X-EDMD)以及20名年龄匹配的正常受试者。所有病例的总氧化状态(TOS)均降低,并且发现大多数患者(82.8%)的总抗氧化能力(TAC)下降。观察到TOS水平与疾病进展之间存在关联。未检测到TOS/TAC水平与心脏或神经学参数之间存在相关性。研究结果表明EDMD患者存在氧化还原平衡紊乱。TOS/TAC的测定可能有助于评估疾病进展以及抗氧化治疗的潜在效果。

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