Suppr超能文献

XJB-5-131 是一种温和的氧化磷酸化解偶联剂。

XJB-5-131 Is a Mild Uncoupler of Oxidative Phosphorylation.

机构信息

Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.

Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

J Huntingtons Dis. 2022;11(2):141-151. doi: 10.3233/JHD-220539.

Abstract

BACKGROUND

Mitochondria (MT) are energy "powerhouses" of the cell and the decline in their function from oxidative damage is strongly correlated in many diseases. To suppress oxygen damage, we have developed and applied XJB-5-131 as a targeted platform for neutralizing reactive oxygen species (ROS) directly in MT. Although the beneficial activity of XJB-5-131 is well documented, the mechanism of its protective effects is not yet fully understood.

OBJECTIVE

Here, we elucidate the mechanism of protection for XJB-5-131, a mitochondrial targeted antioxidant and electron scavenger.

METHODS

The Seahorse Flux Analyzer was used to probe the respiratory states of isolated mouse brain mitochondria treated with XJB-5-131 compared to controls.

RESULTS

Surprisingly, there is no direct impact of XJB-5-131 radical scavenger on the electron flow through the electron transport chain. Rather, XJB-5-131 is a mild uncoupler of oxidative phosphorylation. The nitroxide moiety in XJB-5-131 acts as a superoxide dismutase mimic, which both extracts or donates electrons during redox reactions. The electron scavenging activity of XJB-5-131 prevents the leakage of electrons and reduces formation of superoxide anion, thereby reducing ROS.

CONCLUSION

We show here that XJB-5-131 is a mild uncoupler of oxidative phosphorylation in MT. The mild uncoupling property of XJB-5-131 arises from its redox properties, which exert a protective effect by reducing ROS-induced damage without sacrificing energy production. Because mitochondrial decline is a common and central feature of toxicity, the favorable properties of XJB-5-131 are likely to be useful in treating Huntington's disease and a wide spectrum of neurodegenerative diseases for which oxidative damage is a key component. The mild uncoupling properties of XJB-5-131 suggest a valuable mechanism of action for the design of clinically effective antioxidants.

摘要

背景

线粒体(MT)是细胞的能量“动力源”,其功能的下降与许多疾病中的氧化损伤密切相关。为了抑制氧损伤,我们开发并应用了 XJB-5-131,作为直接在 MT 中中和活性氧(ROS)的靶向平台。尽管 XJB-5-131 的有益活性已有充分记录,但它的保护作用机制尚未完全了解。

目的

本文阐明了 XJB-5-131 的保护机制,XJB-5-131 是一种靶向线粒体的抗氧化剂和电子清除剂。

方法

使用 Seahorse 通量分析仪探测 XJB-5-131 处理的分离小鼠脑线粒体的呼吸状态与对照组相比。

结果

令人惊讶的是,XJB-5-131 自由基清除剂对电子在电子传递链中的流动没有直接影响。相反,XJB-5-131 是一种温和的氧化磷酸化解偶联剂。XJB-5-131 中的硝酮部分作为超氧化物歧化酶模拟物,在氧化还原反应中提取或捐赠电子。XJB-5-131 的电子清除活性可防止电子泄漏并减少超氧阴离子的形成,从而减少 ROS。

结论

我们在这里表明,XJB-5-131 是 MT 中氧化磷酸化的温和解偶联剂。XJB-5-131 的温和解偶联特性源于其氧化还原性质,通过减少 ROS 诱导的损伤而不牺牲能量产生来发挥保护作用。由于线粒体的衰退是毒性的一个常见和核心特征,因此 XJB-5-131 的有利特性可能有助于治疗亨廷顿病和广泛的神经退行性疾病,氧化损伤是这些疾病的关键组成部分。XJB-5-131 的温和解偶联特性为设计临床有效的抗氧化剂提供了有价值的作用机制。

相似文献

10
Huntington's Disease: Astrocytes Shift to Fatty Acid Metabolism.亨廷顿病:星形胶质细胞转向脂肪酸代谢。
Trends Endocrinol Metab. 2019 Sep;30(9):575-577. doi: 10.1016/j.tem.2019.07.019. Epub 2019 Aug 6.

本文引用的文献

8
Metabolic Targets of Coenzyme Q10 in Mitochondria.线粒体中辅酶Q10的代谢靶点
Antioxidants (Basel). 2021 Mar 26;10(4):520. doi: 10.3390/antiox10040520.

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