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Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model

The potential renoprotective effects of vardenafil (VAR) have been evaluated in a very limited number of studies using acute kidney injury animal models other than contrast-induced nephropathy (CIN) with promising results, while avanafil (AVA) has not been evaluated in this respect before. The purpo...

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Autores principales: Zisis, Ioannis-Erineos, Georgiadis, Georgios, Docea, Anca Oana, Calina, Daniela, Cercelaru, Liliana, Tsiaoussis, John, Lazopoulos, Georgios, Sofikitis, Nikolaos, Tsatsakis, Aristidis, Mamoulakis, Charalampos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144719/
https://www.ncbi.nlm.nih.gov/pubmed/35629096
http://dx.doi.org/10.3390/jpm12050670
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author Zisis, Ioannis-Erineos
Georgiadis, Georgios
Docea, Anca Oana
Calina, Daniela
Cercelaru, Liliana
Tsiaoussis, John
Lazopoulos, Georgios
Sofikitis, Nikolaos
Tsatsakis, Aristidis
Mamoulakis, Charalampos
author_facet Zisis, Ioannis-Erineos
Georgiadis, Georgios
Docea, Anca Oana
Calina, Daniela
Cercelaru, Liliana
Tsiaoussis, John
Lazopoulos, Georgios
Sofikitis, Nikolaos
Tsatsakis, Aristidis
Mamoulakis, Charalampos
author_sort Zisis, Ioannis-Erineos
collection PubMed
description The potential renoprotective effects of vardenafil (VAR) have been evaluated in a very limited number of studies using acute kidney injury animal models other than contrast-induced nephropathy (CIN) with promising results, while avanafil (AVA) has not been evaluated in this respect before. The purpose of this study was to evaluate for the first time the potential renoprotective effect of VAR and AVA in a rat model of CIN. Twenty-five male Wistar rats were equally assigned into five groups: control, CIN, CIN+N-acetyl cysteine (NAC) (100 mg/kg/day) as a positive control, CIN+VAR (10 mg/kg/day) and CIN+AVA (50 mg/kg/day). CIN was induced by dehydration, inhibition of prostaglandin and nitric oxide synthesis as well as exposure to the contrast medium (CM). Serum Cr (sCr) levels were measured at 24 and 48 h after CIN induction. At 48 h of CM exposure, animals were sacrificed. Matrix metalloproteinase (MMP) 2 (MMP-2) and MMP-9, kidney injury molecule 1 (KIM-1) and cystatin-C (Cys-C) were measured on renal tissue. Histopathological findings were evaluated on kidney tissue. All treatment groups had close to normal kidney appearance. sCr levels subsided in all treatment groups compared to CIN group at 48 h following CIN induction. A significant decline in the levels of MMP-2, MMP-9, KIM-1 and Cys-C compared to CIN group was observed. These results provide emerging evidence that VAR and AVA may have the potential to prevent CIN.
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spelling pubmed-91447192022-05-29 Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model Zisis, Ioannis-Erineos Georgiadis, Georgios Docea, Anca Oana Calina, Daniela Cercelaru, Liliana Tsiaoussis, John Lazopoulos, Georgios Sofikitis, Nikolaos Tsatsakis, Aristidis Mamoulakis, Charalampos J Pers Med Article The potential renoprotective effects of vardenafil (VAR) have been evaluated in a very limited number of studies using acute kidney injury animal models other than contrast-induced nephropathy (CIN) with promising results, while avanafil (AVA) has not been evaluated in this respect before. The purpose of this study was to evaluate for the first time the potential renoprotective effect of VAR and AVA in a rat model of CIN. Twenty-five male Wistar rats were equally assigned into five groups: control, CIN, CIN+N-acetyl cysteine (NAC) (100 mg/kg/day) as a positive control, CIN+VAR (10 mg/kg/day) and CIN+AVA (50 mg/kg/day). CIN was induced by dehydration, inhibition of prostaglandin and nitric oxide synthesis as well as exposure to the contrast medium (CM). Serum Cr (sCr) levels were measured at 24 and 48 h after CIN induction. At 48 h of CM exposure, animals were sacrificed. Matrix metalloproteinase (MMP) 2 (MMP-2) and MMP-9, kidney injury molecule 1 (KIM-1) and cystatin-C (Cys-C) were measured on renal tissue. Histopathological findings were evaluated on kidney tissue. All treatment groups had close to normal kidney appearance. sCr levels subsided in all treatment groups compared to CIN group at 48 h following CIN induction. A significant decline in the levels of MMP-2, MMP-9, KIM-1 and Cys-C compared to CIN group was observed. These results provide emerging evidence that VAR and AVA may have the potential to prevent CIN. MDPI 2022-04-22 /pmc/articles/PMC9144719/ /pubmed/35629096 http://dx.doi.org/10.3390/jpm12050670 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zisis, Ioannis-Erineos
Georgiadis, Georgios
Docea, Anca Oana
Calina, Daniela
Cercelaru, Liliana
Tsiaoussis, John
Lazopoulos, Georgios
Sofikitis, Nikolaos
Tsatsakis, Aristidis
Mamoulakis, Charalampos
Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title_full Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title_fullStr Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title_full_unstemmed Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title_short Renoprotective Effect of Vardenafil and Avanafil in Contrast-Induced Nephropathy: Emerging Evidence from an Animal Model
title_sort renoprotective effect of vardenafil and avanafil in contrast-induced nephropathy: emerging evidence from an animal model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144719/
https://www.ncbi.nlm.nih.gov/pubmed/35629096
http://dx.doi.org/10.3390/jpm12050670
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