一氧化碳中毒猪幸存者模型脑线粒体损伤的研究。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-01-01 Epub Date: 2023-10-17 DOI:10.1007/s13181-023-00971-1
Constantine D Mavroudis, Alistair Lewis, John C Greenwood, Matthew Kelly, Tiffany S Ko, Rodrigo M Forti, Samuel S Shin, Frances S Shofer, Johannes K Ehinger, Wesley B Baker, Todd J Kilbaugh, David H Jang
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引用次数: 0

摘要

简介:一氧化碳(CO)是一种无色无味的气体,是美国环境中毒的主要原因,造成大量死亡和发病。CO中毒的机制是复杂的,包括缺氧、炎症和脑微血管段的白细胞螯合,导致活性氧物种增加。另一个重要途径是CO对线粒体的影响,特别是对细胞色素c氧化酶的影响,也称为复合物IV(CIV)。其中一个明显的差距是缺乏严格的实验模型,这些模型可以概括急性CO中毒早期的幸存者。这项初步研究的主要目的是利用我们先进的急性CO中毒猪平台开发一个临床相关的幸存者模型,以进行行为评估和MRI成像,这将允许未来开发生物标志物和治疗方法。方法:将4头猪(10 kg)分为两组:对照组(n = 2) 和CO(n = 2) 。CO组接受2000ppm的CO超过120分钟,然后对一只猪在室内空气中再氧化30分钟,对另一只猪再氧化150分钟。假手术组的两只猪接受室内空气150分钟。进行大脑微透析以获得大脑代谢状态的半实时测量。暴露后,对所有存活的动物进行24小时的神经行为评估和成像观察。在24小时结束时,立即采集新鲜的脑组织(皮层和海马)以测量线粒体呼吸。结果:在一项正在进行的初步研究中,CO组的动物在急性暴露期表现出大脑代谢和细胞功能的改变,在CO暴露结束后24小时可能出现持续的线粒体变化。结论:这项初步研究进一步建立了一个大型动物猪模型,调查CO中毒幸存者,以测量与临床医学相关的转化指标,包括基本的神经行为评估和暴露后的细胞测量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of Cerebral Mitochondrial Injury in a Porcine Survivor Model of Carbon Monoxide Poisoning.

Introduction: Carbon monoxide (CO) is a colorless and odorless gas that is a leading cause of environmental poisoning in the USA with substantial mortality and morbidity. The mechanism of CO poisoning is complex and includes hypoxia, inflammation, and leukocyte sequestration in brain microvessel segments leading to increased reactive oxygen species. Another important pathway is the effects of CO on the mitochondria, specifically at cytochrome c oxidase, also known as Complex IV (CIV). One of the glaring gaps is the lack of rigorous experimental models that may recapitulate survivors of acute CO poisoning in the early phase. The primary objective of this preliminary study is to use our advanced swine platform of acute CO poisoning to develop a clinically relevant survivor model to perform behavioral assessment and MRI imaging that will allow future development of biomarkers and therapeutics.

Methods: Four swine (10 kg) were divided into two groups: control (n = 2) and CO (n = 2). The CO group received CO at 2000 ppm for over 120 min followed by 30 min of re-oxygenation at room air for one swine and 150 min followed by 30 min of re-oxygenation for another swine. The two swine in the sham group received room air for 150 min. Cerebral microdialysis was performed to obtain semi real-time measurements of cerebral metabolic status. Following exposures, all surviving animals were observed for a 24-h period with neurobehavioral assessment and imaging. At the end of the 24-h period, fresh brain tissue (cortical and hippocampal) was immediately harvested to measure mitochondrial respiration.

Results: While a preliminary ongoing study, animals in the CO group showed alterations in cerebral metabolism and cellular function in the acute exposure phase with possible sustained mitochondrial changes 24 h after the CO exposure ended.

Conclusions: This preliminary research further establishes a large animal swine model investigating survivors of CO poisoning to measure translational metrics relevant to clinical medicine that includes a basic neurobehavioral assessment and post exposure cellular measures.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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