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Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality

Oxidative stress and multiple erythrocyte abnormalities have been observed in hypertension. We focused on the effects of angiotensin-converting enzyme 2 (ACE2) inhibition by MLN-4760 inhibitor on angiotensin peptides, oxidative stress parameters, and selected erythrocyte quality markers in spontaneo...

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Autores principales: Jasenovec, Tomas, Radosinska, Dominika, Kollarova, Marta, Balis, Peter, Zorad, Stefan, Vrbjar, Norbert, Bernatova, Iveta, Cacanyiova, Sona, Tothova, Lubomira, Radosinska, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788412/
https://www.ncbi.nlm.nih.gov/pubmed/36556410
http://dx.doi.org/10.3390/life12122045
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author Jasenovec, Tomas
Radosinska, Dominika
Kollarova, Marta
Balis, Peter
Zorad, Stefan
Vrbjar, Norbert
Bernatova, Iveta
Cacanyiova, Sona
Tothova, Lubomira
Radosinska, Jana
author_facet Jasenovec, Tomas
Radosinska, Dominika
Kollarova, Marta
Balis, Peter
Zorad, Stefan
Vrbjar, Norbert
Bernatova, Iveta
Cacanyiova, Sona
Tothova, Lubomira
Radosinska, Jana
author_sort Jasenovec, Tomas
collection PubMed
description Oxidative stress and multiple erythrocyte abnormalities have been observed in hypertension. We focused on the effects of angiotensin-converting enzyme 2 (ACE2) inhibition by MLN-4760 inhibitor on angiotensin peptides, oxidative stress parameters, and selected erythrocyte quality markers in spontaneously hypertensive rats (SHR). We also investigated the potential effects of polyphenolic antioxidant taxifolin when applied in vivo and in vitro following its incubation with erythrocytes. SHRs were divided into four groups: control, taxifolin-treated, MLN-4760-treated, and MLN-4760 with taxifolin. MLN-4760 administration increased the blood pressure rise independent of taxifolin treatment, whereas taxifolin decreased it in control SHRs. Body weight gain was also higher in ACE2-inhibited animals and normalized after taxifolin treatment. However, taxifolin did not induce any change in angiotensin peptide concentrations nor a clear antioxidant effect. We documented an increase in Na,K-ATPase enzyme activity in erythrocyte membranes of ACE2-inhibited SHRs after taxifolin treatment. In conclusion, ACE2 inhibition deteriorated some selected RBC properties in SHRs. Although taxifolin treatment did not improve oxidative stress markers, our data confirmed the blood pressure-lowering potential, anti-obesogenic effect, and some “erythroprotective” effects of this compound in both control and ACE2-inhibited SHRs. In vitro investigations documenting different effects of taxifolin on erythrocyte properties from control and ACE2-inhibited SHRs accentuated the irreplaceability of in vivo studies.
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spelling pubmed-97884122022-12-24 Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality Jasenovec, Tomas Radosinska, Dominika Kollarova, Marta Balis, Peter Zorad, Stefan Vrbjar, Norbert Bernatova, Iveta Cacanyiova, Sona Tothova, Lubomira Radosinska, Jana Life (Basel) Article Oxidative stress and multiple erythrocyte abnormalities have been observed in hypertension. We focused on the effects of angiotensin-converting enzyme 2 (ACE2) inhibition by MLN-4760 inhibitor on angiotensin peptides, oxidative stress parameters, and selected erythrocyte quality markers in spontaneously hypertensive rats (SHR). We also investigated the potential effects of polyphenolic antioxidant taxifolin when applied in vivo and in vitro following its incubation with erythrocytes. SHRs were divided into four groups: control, taxifolin-treated, MLN-4760-treated, and MLN-4760 with taxifolin. MLN-4760 administration increased the blood pressure rise independent of taxifolin treatment, whereas taxifolin decreased it in control SHRs. Body weight gain was also higher in ACE2-inhibited animals and normalized after taxifolin treatment. However, taxifolin did not induce any change in angiotensin peptide concentrations nor a clear antioxidant effect. We documented an increase in Na,K-ATPase enzyme activity in erythrocyte membranes of ACE2-inhibited SHRs after taxifolin treatment. In conclusion, ACE2 inhibition deteriorated some selected RBC properties in SHRs. Although taxifolin treatment did not improve oxidative stress markers, our data confirmed the blood pressure-lowering potential, anti-obesogenic effect, and some “erythroprotective” effects of this compound in both control and ACE2-inhibited SHRs. In vitro investigations documenting different effects of taxifolin on erythrocyte properties from control and ACE2-inhibited SHRs accentuated the irreplaceability of in vivo studies. MDPI 2022-12-07 /pmc/articles/PMC9788412/ /pubmed/36556410 http://dx.doi.org/10.3390/life12122045 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
Jasenovec, Tomas
Radosinska, Dominika
Kollarova, Marta
Balis, Peter
Zorad, Stefan
Vrbjar, Norbert
Bernatova, Iveta
Cacanyiova, Sona
Tothova, Lubomira
Radosinska, Jana
Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title_full Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title_fullStr Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title_full_unstemmed Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title_short Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality
title_sort effects of taxifolin in spontaneously hypertensive rats with a focus on erythrocyte quality
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9788412/
https://www.ncbi.nlm.nih.gov/pubmed/36556410
http://dx.doi.org/10.3390/life12122045
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