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Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression

The progression of an abdominal aortic aneurysm (AAA) is an important issue, especially as AAA is becoming more common, and potentially life-threatening. This study aimed to understand better the mechanisms underlying AAA progression. For this purpose, we have focused on assessing the selected bioma...

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Autores principales: Kasprzak, Magdalena P., Gryszczyńska, Bogna, Olasińska-Wiśniewska, Anna, Urbanowicz, Tomasz, Jawień, Andrzej, Krasiński, Zbigniew, Formanowicz, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451880/
https://www.ncbi.nlm.nih.gov/pubmed/37627563
http://dx.doi.org/10.3390/antiox12081568
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author Kasprzak, Magdalena P.
Gryszczyńska, Bogna
Olasińska-Wiśniewska, Anna
Urbanowicz, Tomasz
Jawień, Andrzej
Krasiński, Zbigniew
Formanowicz, Dorota
author_facet Kasprzak, Magdalena P.
Gryszczyńska, Bogna
Olasińska-Wiśniewska, Anna
Urbanowicz, Tomasz
Jawień, Andrzej
Krasiński, Zbigniew
Formanowicz, Dorota
author_sort Kasprzak, Magdalena P.
collection PubMed
description The progression of an abdominal aortic aneurysm (AAA) is an important issue, especially as AAA is becoming more common, and potentially life-threatening. This study aimed to understand better the mechanisms underlying AAA progression. For this purpose, we have focused on assessing the selected biomarkers whose potentially common denominator is the NRF2 (nuclear factor erythroid 2-related factor 2) transcription factor, that determines the selected antioxidant enzymes’ activation. The study group consisted of 44 AAA male patients (71.41 ± 7.80 years aged). They were divided into three groups based on the aneurism diameter: group I (below 55 mm), group II (between 55 and 70 mm), and group III (over 70 mm). The laboratory analyses of PON1 (paraoxonase-1), NRF2, and HO-1 (heme oxygenase 1) were performed based on commercial ELISA tests; Blb (bilirubin) and hsCRP (high sensitivity C-reactive protein) were assessed during routine morphology examinations after admission to the hospital. Multiple linear regression showed that both bilirubin and NRF2 determined the PON1 concentration in the entire study group. The correlations between the examined parameters within the three studied groups suggest the capitulation of NRF2-dependent antioxidant mechanisms to pro-inflammatory processes. We showed that HO-1 and hsCRP may play a crucial role in the development of inflammation aneurism progression. Moreover, in patients with medium-sized aneurysms, antioxidant mechanisms were depressed, and inflammatory processes began to dominate, which may lead to uncontrolled growth aneurysm rupture. Our study is one of the first to indicate that the chronically activated antioxidant pathway using NRF2 may be a source of reduction stress.
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spelling pubmed-104518802023-08-26 Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression Kasprzak, Magdalena P. Gryszczyńska, Bogna Olasińska-Wiśniewska, Anna Urbanowicz, Tomasz Jawień, Andrzej Krasiński, Zbigniew Formanowicz, Dorota Antioxidants (Basel) Article The progression of an abdominal aortic aneurysm (AAA) is an important issue, especially as AAA is becoming more common, and potentially life-threatening. This study aimed to understand better the mechanisms underlying AAA progression. For this purpose, we have focused on assessing the selected biomarkers whose potentially common denominator is the NRF2 (nuclear factor erythroid 2-related factor 2) transcription factor, that determines the selected antioxidant enzymes’ activation. The study group consisted of 44 AAA male patients (71.41 ± 7.80 years aged). They were divided into three groups based on the aneurism diameter: group I (below 55 mm), group II (between 55 and 70 mm), and group III (over 70 mm). The laboratory analyses of PON1 (paraoxonase-1), NRF2, and HO-1 (heme oxygenase 1) were performed based on commercial ELISA tests; Blb (bilirubin) and hsCRP (high sensitivity C-reactive protein) were assessed during routine morphology examinations after admission to the hospital. Multiple linear regression showed that both bilirubin and NRF2 determined the PON1 concentration in the entire study group. The correlations between the examined parameters within the three studied groups suggest the capitulation of NRF2-dependent antioxidant mechanisms to pro-inflammatory processes. We showed that HO-1 and hsCRP may play a crucial role in the development of inflammation aneurism progression. Moreover, in patients with medium-sized aneurysms, antioxidant mechanisms were depressed, and inflammatory processes began to dominate, which may lead to uncontrolled growth aneurysm rupture. Our study is one of the first to indicate that the chronically activated antioxidant pathway using NRF2 may be a source of reduction stress. MDPI 2023-08-05 /pmc/articles/PMC10451880/ /pubmed/37627563 http://dx.doi.org/10.3390/antiox12081568 Text en © 2023 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
Kasprzak, Magdalena P.
Gryszczyńska, Bogna
Olasińska-Wiśniewska, Anna
Urbanowicz, Tomasz
Jawień, Andrzej
Krasiński, Zbigniew
Formanowicz, Dorota
Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title_full Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title_fullStr Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title_full_unstemmed Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title_short Blb-NRF2-PON1 Cross-Talk in Abdominal Aortic Aneurysm Progression
title_sort blb-nrf2-pon1 cross-talk in abdominal aortic aneurysm progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451880/
https://www.ncbi.nlm.nih.gov/pubmed/37627563
http://dx.doi.org/10.3390/antiox12081568
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