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The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?

PURPOSE: Continuous oxygen therapy to compensate for decreased oxygen saturation in the blood is a life-saving treatment used in case lung involvement. Excess oxygen delivery was reported to be a common situation, in which about 50% of the patients showed hyperoxemia and 4% in severe hyperoxemia. In...

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Autores principales: Kilicarslan, Nermin, Demir, Aslan, Yeni, Sezgin, Cicek, Mehmet Cagatay, Saricetin, Aysun, Dirican, Melahat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707269/
https://www.ncbi.nlm.nih.gov/pubmed/36443608
http://dx.doi.org/10.1007/s11255-022-03416-w
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author Kilicarslan, Nermin
Demir, Aslan
Yeni, Sezgin
Cicek, Mehmet Cagatay
Saricetin, Aysun
Dirican, Melahat
author_facet Kilicarslan, Nermin
Demir, Aslan
Yeni, Sezgin
Cicek, Mehmet Cagatay
Saricetin, Aysun
Dirican, Melahat
author_sort Kilicarslan, Nermin
collection PubMed
description PURPOSE: Continuous oxygen therapy to compensate for decreased oxygen saturation in the blood is a life-saving treatment used in case lung involvement. Excess oxygen delivery was reported to be a common situation, in which about 50% of the patients showed hyperoxemia and 4% in severe hyperoxemia. In this work, we investigated the effects of hyperoxia on the rat kidneys and whether tadalafil has an effect to reduce this damage. MATERIALS AND METHODS: Three groups of 8 male rats each weighing 300–350 g were formed. The groups were divided into the control group, hyperoxia group, and hyperoxia and tadalafil administered group for 10 days. At the end of the 10th day, blood and kidney samples were taken for biochemical analysis (SOD and NO levels) and histopathological examination. RESULTS: While our findings showed that SOD levels were significantly different among the control and experimental groups and within the experimental groups, no statistical difference was found in terms of NO levels among the groups (Table 1). While the glomerular and tubular injury was higher in the Hyperoxia group and the Hyperoxia + Tadalafil group than in the control group (p < 0.001), as a result of the rate of severe glomerular and tubular injury in the hyperoxia group, was 62.5% and 43.8% and in the group given tadalafil was 43.8% and 31.3%, respectively (Table 2). CONCLUSIONS: Exposure to hyperoxia condition causes renal glomerular and tubular damage, and tadalafil does not show a protective effect on this damage according to this study’s dose and exposure time.
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spelling pubmed-97072692022-11-29 The danger of hyperoxia on the rat kidneys: is tadalafil a real shield? Kilicarslan, Nermin Demir, Aslan Yeni, Sezgin Cicek, Mehmet Cagatay Saricetin, Aysun Dirican, Melahat Int Urol Nephrol Urology - Original Paper PURPOSE: Continuous oxygen therapy to compensate for decreased oxygen saturation in the blood is a life-saving treatment used in case lung involvement. Excess oxygen delivery was reported to be a common situation, in which about 50% of the patients showed hyperoxemia and 4% in severe hyperoxemia. In this work, we investigated the effects of hyperoxia on the rat kidneys and whether tadalafil has an effect to reduce this damage. MATERIALS AND METHODS: Three groups of 8 male rats each weighing 300–350 g were formed. The groups were divided into the control group, hyperoxia group, and hyperoxia and tadalafil administered group for 10 days. At the end of the 10th day, blood and kidney samples were taken for biochemical analysis (SOD and NO levels) and histopathological examination. RESULTS: While our findings showed that SOD levels were significantly different among the control and experimental groups and within the experimental groups, no statistical difference was found in terms of NO levels among the groups (Table 1). While the glomerular and tubular injury was higher in the Hyperoxia group and the Hyperoxia + Tadalafil group than in the control group (p < 0.001), as a result of the rate of severe glomerular and tubular injury in the hyperoxia group, was 62.5% and 43.8% and in the group given tadalafil was 43.8% and 31.3%, respectively (Table 2). CONCLUSIONS: Exposure to hyperoxia condition causes renal glomerular and tubular damage, and tadalafil does not show a protective effect on this damage according to this study’s dose and exposure time. Springer Netherlands 2022-11-29 2023 /pmc/articles/PMC9707269/ /pubmed/36443608 http://dx.doi.org/10.1007/s11255-022-03416-w Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Urology - Original Paper
Kilicarslan, Nermin
Demir, Aslan
Yeni, Sezgin
Cicek, Mehmet Cagatay
Saricetin, Aysun
Dirican, Melahat
The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title_full The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title_fullStr The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title_full_unstemmed The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title_short The danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
title_sort danger of hyperoxia on the rat kidneys: is tadalafil a real shield?
topic Urology - Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707269/
https://www.ncbi.nlm.nih.gov/pubmed/36443608
http://dx.doi.org/10.1007/s11255-022-03416-w
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