The Nephroprotective Effect of Nitric Oxide during Extracorporeal Circulation: An Experimental Study
Autor: | Nikolay O. Kamenshchikov, Yuri K. Podoksenov, Boris N. Kozlov, Leonid N. Maslov, Alexander V. Mukhomedzyanov, Mark A. Tyo, Alexander M. Boiko, Natalya Yu. Margolis, Alla A. Boshchenko, Olga N. Serebryakova, Anna N. Dzyuman, Alexander S. Shirshin, Sergey N. Buranov, Victor D. Selemir |
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Jazyk: | angličtina |
Rok vydání: | 2024 |
Předmět: | |
Zdroj: | Biomedicines, Vol 12, Iss 6, p 1298 (2024) |
Druh dokumentu: | article |
ISSN: | 12061298 2227-9059 88935329 |
DOI: | 10.3390/biomedicines12061298 |
Popis: | This study aims to determine the effectiveness of administering 80 ppm nitric oxide in reducing kidney injury, mitochondrial dysfunction and regulated cell death in kidneys during experimental perfusion. Twenty-four sheep were randomized into four groups: two groups received 80 ppm NO conditioning with 90 min of cardiopulmonary bypass (CPB + NO) or 90 min of CPB and hypothermic circulatory arrest (CPB + CA + NO), while two groups received sham protocols (CPB and CPB + CA). Kidney injury was assessed using laboratory (neutrophil gelatinase-associated lipocalin, an acute kidney injury biomarker) and morphological methods (morphometric histological changes in kidney biopsy specimens). A kidney biopsy was performed 60 min after weaning from mechanical perfusion. NO did not increase the concentrations of inhaled NO2 and methemoglobin significantly. The NO-conditioning groups showed less severe kidney injury and mitochondrial dysfunction, with statistical significance in the CPB + NO group and reduced tumor necrosis factor-α expression as a trigger of apoptosis and necroptosis in renal tissue in the CPB + CA + NO group compared to the CPB + CA group. The severity of mitochondrial dysfunction in renal tissue was insignificantly lower in the NO-conditioning groups. We conclude that NO administration is safe and effective at reducing kidney injury, mitochondrial dysfunction and regulated cell death in kidneys during experimental CPB. |
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