用1GHz快速扫描电子顺磁共振成像通过与羟胺探针反应捕获的小鼠肺中的活性氧自由基。

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Molecular Imaging and Biology Pub Date : 2024-06-01 Epub Date: 2023-10-11 DOI:10.1007/s11307-023-01860-3
Hanan B Elajaili, Lukas B Woodcock, Tanden A Hovey, George A Rinard, Samuel DeGraw, Autumn Canny, Nathan M Dee, Joseph P Y Kao, Eva S Nozik, Sandra S Eaton, Gareth R Eaton
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引用次数: 0

摘要

目的:氧化应激被认为是急性肺部疾病的关键,但缺乏监测肺部自由基的方法。我们的目标是开发低频电子顺磁共振(EPR)方法来监测导致疾病的自由基。程序:脂多糖诱导的急性呼吸窘迫综合征小鼠模型中产生的自由基与环状羟胺CPH(1-羟基-3-羧基-2,2,5,5-四甲基吡咯烷盐酸盐)和DCP-AM-H(4-乙酰氧基甲氧羰基-1-羟基-2,2,5-四甲基吡咯烷-3-羧酸)反应,转化为相应的氮氧化物自由基,CP•和DCP•。用采用快速扫描技术的1GHz EPR光谱仪/成像器对切除肺中的氮氧化物自由基的EPR信号进行成像。结果:羟胺和超氧化物反应生成的少量氮氧化物导致光谱和图像的信噪比较低。然而,由于氮氧化物的光谱性质是已知的,我们可以使用线形和超精细分裂的先验知识来拟合噪声数据,从而产生定义明确的光谱和图像。显示了含有(4.5±0.5)×1014 CP•和(9.9±1.0)×1014DCP•氮氧化物自旋的肺部样本的二维光谱空间图像。这些结果表明,在细胞中积累的探针比更容易从细胞中冲洗出来的探针提供更强的氮氧化物信号。结论:与羟胺探针CPH和DCP-AM-H反应形成的离体小鼠肺中的氮氧化物自由基可以在1GHz下成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Imaging Reactive Oxygen Radicals in Excised Mouse Lung Trapped by Reaction with Hydroxylamine Probes Using 1 GHz Rapid Scan Electron Paramagnetic Resonance.

Purpose: Oxidative stress is proposed to be critical in acute lung disease, but methods to monitor radicals in lungs are lacking. Our goal is to develop low-frequency electron paramagnetic resonance (EPR) methods to monitor radicals that contribute to the disease.

Procedures: Free radicals generated in a lipopolysaccharide-induced mouse model of acute respiratory distress syndrome reacted with cyclic hydroxylamines CPH (1-hydroxy-3-carboxy-2,2,5,5-tetramethylpyrrolidine hydrochloride) and DCP-AM-H (4-acetoxymethoxycarbonyl-1-hydroxy-2,2,5,5-tetramethylpyrrolidine-3-carboxylic acid), which were converted into the corresponding nitroxide radicals, CP• and DCP•. The EPR signals of the nitroxide radicals in excised lungs were imaged with a 1 GHz EPR spectrometer/imager that employs rapid scan technology.

Results: The small numbers of nitroxides formed by reaction of the hydroxylamine with superoxide result in low signal-to-noise in the spectra and images. However, since the spectral properties of the nitroxides are known, we can use prior knowledge of the line shape and hyperfine splitting to fit the noisy data, yielding well-defined spectra and images. Two-dimensional spectral-spatial images are shown for lung samples containing (4.5 ± 0.5) ×1014 CP• and (9.9 ± 1.0) ×1014 DCP• nitroxide spins. These results suggest that a probe that accumulates in cells gives a stronger nitroxide signal than a probe that is more easily washed out of cells.

Conclusion: The nitroxide radicals in excised mouse lungs formed by reaction with hydroxylamine probes CPH and DCP-AM-H can be imaged at 1 GHz.

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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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