共振拉曼光谱在啮齿类动物主动脉实验性缩窄模型中检测缺血。

IF 2.4 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Alyssa R Thomas, Kristen Lazelle, Julia Garcia Mancebo, Padraic Romfh, John N Kheir
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引用次数: 0

摘要

主动脉缩窄(CoA)可引起主动脉阻塞、缺血和死亡。共振拉曼光谱(RRS)无创测量组织氧合血红蛋白(ShbO2)和线粒体氧化还原状态(3RMR)。在大鼠主动脉周围放置金属丝,产生收缩压梯度。在阻塞前(手)和阻塞后(足)分别测定RRS-ShbO2和3RMR。在模型1 (n = 8)中,梯度迅速达到120 mmHg。在模型2 (n = 30)中,维持20 mmHg (n = 9)和40 mmHg (n = 12)梯度2小时。在模型1中,当收缩压梯度为80 mmHg或更高时,foot-ShbO2和3RMR发生显著变化(P = 0.004和P = 0.007)。在模型2中,40-mmHg梯度组1小时后,foot-ShbO2显著下降(P = 0.014), 3RMR显著升高(P = 0.008)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resonance Raman Spectroscopy Detects Ischemia in Experimental Coarctation of the Aorta in a Rodent Model.

Coarctation of the aorta (CoA) can cause aortic obstruction, ischemia, and death. Resonance Raman Spectroscopy (RRS) measures tissue oxyhemoglobin (ShbO2) and mitochondrial redox state (3RMR) non-invasively. Metal wire was placed around the aorta of Sprague Dawley rats to generate a systolic blood pressure (SBP) gradient. RRS-ShbO2 and 3RMR were measured pre- (hand) and post-obstruction (foot). In model 1 (n = 8), the gradient rapidly reached 120 mmHg. In model 2 (n = 30), gradients of 20 mmHg (n = 9) and 40 mmHg (n = 12) were maintained for 2 h. In model 1, foot-ShbO2 and 3RMR changed significantly (P = 0.004 and P = 0.007) at SBP gradients of 80-mmHg or above. In model 2, the 40-mmHg gradient group showed significant declines in foot-ShbO2 (P = 0.014) and increases in 3RMR (P = 0.008) by 1 h. Foot-ShbO2 and 3RMR correlated strongly with serum mixed venous saturation (ShbO2: r = 0.73, P < 0.0001; 3RMR: r = -0.55, P < 0.0001). RRS effectively detects ischemia caused by aortic obstruction in a CoA model.

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来源期刊
Journal of Cardiovascular Translational Research
Journal of Cardiovascular Translational Research CARDIAC & CARDIOVASCULAR SYSTEMS-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
6.10
自引率
2.90%
发文量
148
审稿时长
6-12 weeks
期刊介绍: Journal of Cardiovascular Translational Research (JCTR) is a premier journal in cardiovascular translational research. JCTR is the journal of choice for authors seeking the broadest audience for emerging technologies, therapies and diagnostics, pre-clinical research, and first-in-man clinical trials. JCTR''s intent is to provide a forum for critical evaluation of the novel cardiovascular science, to showcase important and clinically relevant aspects of the new research, as well as to discuss the impediments that may need to be overcome during the translation to patient care.
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