Suppr超能文献

脓毒症中的细胞色素c氧化酶功能障碍。

Cytochrome c oxidase dysfunction in sepsis.

作者信息

Levy Richard J, Deutschman Clifford S

机构信息

New York Medical College and Maria Fareri Children's Hospital at Westchester Medical Center, Valhalla, NY, USA.

出版信息

Crit Care Med. 2007 Sep;35(9 Suppl):S468-75. doi: 10.1097/01.CCM.0000278604.93569.27.

Abstract

Sepsis, the principal cause of death in critically ill patients, is associated with impaired oxygen extraction by tissues. One possible explanation is the development of mitochondrial dysfunction and ineffective oxygen utilization. This abnormality has been termed cytopathic hypoxia. This may be caused by an abnormality in the transport of electrons down the cytochrome chain on the mitochondrial inner membrane. In this article we review our studies on abnormalities in the function of complex IV (cytochrome oxidase), the final electron acceptor in this chain. In addition, we provide evidence that administration of cytochrome c may overcome these abnormalities and provide a novel therapeutic alternative.

摘要

脓毒症是重症患者死亡的主要原因,与组织氧摄取受损有关。一种可能的解释是线粒体功能障碍和氧利用效率低下的发展。这种异常被称为细胞病性缺氧。这可能是由于线粒体内膜上细胞色素链电子传递异常所致。在本文中,我们回顾了我们对该链中最终电子受体复合物IV(细胞色素氧化酶)功能异常的研究。此外,我们提供证据表明,给予细胞色素c可能克服这些异常,并提供一种新的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验