Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol

We used a mitochondria-penetrating nitroxide, mito-TEMPO, as a contrast probe for imaging of kidney dysfunction in mice, based on the redox-imbalance and oxidative stress in the renal tissues. Kidney dysfunction was triggered by hypercholesterolemia. The mice were divided in three groups: (i) on nor...

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Main Authors: Dessislava Lazarova, Sayaka Shibata, Itsuko Ishii, Genoveva Zlateva, Zhivko Zhelev, Ichio Aoki, Rumiana Bakalova
Format: Article
Language:English
Published: Taylor & Francis Group 2019-01-01
Series:Biotechnology & Biotechnological Equipment
Subjects:
Online Access:http://dx.doi.org/10.1080/13102818.2019.1573153
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author Dessislava Lazarova
Sayaka Shibata
Itsuko Ishii
Genoveva Zlateva
Zhivko Zhelev
Ichio Aoki
Rumiana Bakalova
author_facet Dessislava Lazarova
Sayaka Shibata
Itsuko Ishii
Genoveva Zlateva
Zhivko Zhelev
Ichio Aoki
Rumiana Bakalova
author_sort Dessislava Lazarova
collection DOAJ
description We used a mitochondria-penetrating nitroxide, mito-TEMPO, as a contrast probe for imaging of kidney dysfunction in mice, based on the redox-imbalance and oxidative stress in the renal tissues. Kidney dysfunction was triggered by hypercholesterolemia. The mice were divided in three groups: (i) on normal diet (ND; control); (ii) on cholesterol diet (CD); (iii) on cholesterol plus cholestyramine diet (CC). CD mice showed increased plasma levels of total cholesterol and non-HDL-cholesterol, as well as increased serum levels of blood urea nitrogen, uric acid and creatinine, compared to ND mice. CC mice showed slightly increased plasma levels of total cholesterol and HDL-cholesterol, but not non-HDL-cholesterol, compared to ND mice. The serum levels of blood urea nitrogen, uric acid and creatinine in CC mice were equal to those in ND mice. The MRI signal of mito-TEMPO in the kidneys was characterized by: high intensity and long life-time in CD mice, indicating a high oxidative capacity of renal tissues; poor intensity and short life-time in ND mice, indicating a high reducing capacity of renal tissues; moderate intensity and relatively short life-time in CC mice, which shows the protective effect of lipid-lowering agents against oxidative damage. The data suggest that hypercholesterolemia induces redox-imbalance and oxidative stress in kidneys and this process could be visualized using MRI and mito-TEMPO as a redox-sensitive contrast substance.
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spelling doaj.art-c2ed0ada69e44e6a9a510dc947734f902022-12-22T00:16:44ZengTaylor & Francis GroupBiotechnology & Biotechnological Equipment1310-28181314-35302019-01-0133129430110.1080/13102818.2019.15731531573153Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterolDessislava Lazarova0Sayaka Shibata1Itsuko Ishii2Genoveva Zlateva3Zhivko Zhelev4Ichio Aoki5Rumiana Bakalova6Sofia University “St. Kliment Ohridski”National Institute of Radiological Sciences (QST-NIRS)Chiba UniversitySofia University “St. Kliment Ohridski”Trakia UniversityNational Institute of Radiological Sciences (QST-NIRS)Sofia University “St. Kliment Ohridski”We used a mitochondria-penetrating nitroxide, mito-TEMPO, as a contrast probe for imaging of kidney dysfunction in mice, based on the redox-imbalance and oxidative stress in the renal tissues. Kidney dysfunction was triggered by hypercholesterolemia. The mice were divided in three groups: (i) on normal diet (ND; control); (ii) on cholesterol diet (CD); (iii) on cholesterol plus cholestyramine diet (CC). CD mice showed increased plasma levels of total cholesterol and non-HDL-cholesterol, as well as increased serum levels of blood urea nitrogen, uric acid and creatinine, compared to ND mice. CC mice showed slightly increased plasma levels of total cholesterol and HDL-cholesterol, but not non-HDL-cholesterol, compared to ND mice. The serum levels of blood urea nitrogen, uric acid and creatinine in CC mice were equal to those in ND mice. The MRI signal of mito-TEMPO in the kidneys was characterized by: high intensity and long life-time in CD mice, indicating a high oxidative capacity of renal tissues; poor intensity and short life-time in ND mice, indicating a high reducing capacity of renal tissues; moderate intensity and relatively short life-time in CC mice, which shows the protective effect of lipid-lowering agents against oxidative damage. The data suggest that hypercholesterolemia induces redox-imbalance and oxidative stress in kidneys and this process could be visualized using MRI and mito-TEMPO as a redox-sensitive contrast substance.http://dx.doi.org/10.1080/13102818.2019.1573153hypercholesterolemiakidney dysfunctionredox-imbalanceoxidative stressmagnetic resonance imagingcyclic nitroxides
spellingShingle Dessislava Lazarova
Sayaka Shibata
Itsuko Ishii
Genoveva Zlateva
Zhivko Zhelev
Ichio Aoki
Rumiana Bakalova
Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
Biotechnology & Biotechnological Equipment
hypercholesterolemia
kidney dysfunction
redox-imbalance
oxidative stress
magnetic resonance imaging
cyclic nitroxides
title Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
title_full Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
title_fullStr Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
title_full_unstemmed Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
title_short Imaging of redox-imbalance and oxidative stress in kidney in vivo, induced by dietary cholesterol
title_sort imaging of redox imbalance and oxidative stress in kidney in vivo induced by dietary cholesterol
topic hypercholesterolemia
kidney dysfunction
redox-imbalance
oxidative stress
magnetic resonance imaging
cyclic nitroxides
url http://dx.doi.org/10.1080/13102818.2019.1573153
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