Open Access
19 April 2012 Optical imaging of tissue mitochondrial redox state in intact rat lungs in two models of pulmonary oxidative stress
Reyhaneh Sepehr, Kevin Staniszewski, Sepideh Maleki, Mahsa Ranji, Elizabeth R. Jacobs, Said Audi
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Abstract
Ventilation with enhanced fractions of O2 (hyperoxia) is a common and necessary treatment for hypoxemia in patients with lung failure, but prolonged exposure to hyperoxia causes lung injury. Ischemia-reperfusion (IR) injury of lung tissue is common in lung transplant or crush injury to the chest. These conditions are associated with apoptosis and decreased survival of lung tissue. The objective of this work is to use cryoimaging to evaluate the effect of exposure to hyperoxia and IR injury on lung tissue mitochondrial redox state in rats. The autofluorescent mitochondrial metabolic coenzymes nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) are electron carriers in ATP generation. These intrinsic fluorophores were imaged for rat lungs using low-temperature fluorescence imaging (cryoimaging). Perfused lungs from four groups of rats were studied: normoxia (control), control perfused with an mitochondrial complex IV inhibitor (potassium cyanide, KCN), rats exposed to hyperoxia (85% O2) for seven days, and from rats subjected to lung IR in vivo 24 hours prior to study. Each lung was sectioned sequentially in the transverse direction, and the images were used to reconstruct a three-dimensional (3-D) rendering. In KCN perfused lungs the respiratory chain was more reduced, whereas hyperoxic and IR lung tissue have a more oxidized respiratory chain than control lung tissue, consistent with previously measured mitochondrial dysfunction in both hyperoxic and IR lungs.
© 2012 Society of Photo-Optical Instrumentation Engineers (SPIE) 0091-3286/2012/$25.00 © 2012 SPIE
Reyhaneh Sepehr, Kevin Staniszewski, Sepideh Maleki, Mahsa Ranji, Elizabeth R. Jacobs, and Said Audi "Optical imaging of tissue mitochondrial redox state in intact rat lungs in two models of pulmonary oxidative stress," Journal of Biomedical Optics 17(4), 046010 (19 April 2012). https://doi.org/10.1117/1.JBO.17.4.046010
Published: 19 April 2012
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Cited by 41 scholarly publications.
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KEYWORDS
Lung

Tissues

Injuries

Tissue optics

Luminescence

Hyperoxia

Optical imaging

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