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PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients

Pituitary adenylate cyclase activating polypeptide-38 (PACAP-38) is a multifunctional neuropeptide, which may play a role in cardioprotection. However, little is known about the presence of PACAP-38 in heart failure (HF) patients. The aim of our study was to measure the alterations of PACAP-38 like...

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Autores principales: Szabó, Dóra, Sárszegi, Zsolt, Polgár, Beáta, Sághy, Éva, Reglődi, Dóra, Tóth, Tünde, Onódi, Zsófia, Leszek, Przemyslaw, Varga, Zoltán V., Helyes, Zsuzsanna, Kemény, Ágnes, Ferdinandy, Péter, Tamás, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998504/
https://www.ncbi.nlm.nih.gov/pubmed/35409075
http://dx.doi.org/10.3390/ijms23073715
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author Szabó, Dóra
Sárszegi, Zsolt
Polgár, Beáta
Sághy, Éva
Reglődi, Dóra
Tóth, Tünde
Onódi, Zsófia
Leszek, Przemyslaw
Varga, Zoltán V.
Helyes, Zsuzsanna
Kemény, Ágnes
Ferdinandy, Péter
Tamás, Andrea
author_facet Szabó, Dóra
Sárszegi, Zsolt
Polgár, Beáta
Sághy, Éva
Reglődi, Dóra
Tóth, Tünde
Onódi, Zsófia
Leszek, Przemyslaw
Varga, Zoltán V.
Helyes, Zsuzsanna
Kemény, Ágnes
Ferdinandy, Péter
Tamás, Andrea
author_sort Szabó, Dóra
collection PubMed
description Pituitary adenylate cyclase activating polypeptide-38 (PACAP-38) is a multifunctional neuropeptide, which may play a role in cardioprotection. However, little is known about the presence of PACAP-38 in heart failure (HF) patients. The aim of our study was to measure the alterations of PACAP-38 like immunoreactivity (LI) in acute (n = 13) and chronic HF (n = 33) and to examine potential correlations between PACAP-38 and HF predictors (cytokines, NT-proBNP). Tissue PACAP-38 LI and PAC1 receptor levels were also investigated in heart tissue samples of patients with HF. Significantly higher plasma PACAP-38 LI was detected in patients with acute HF, while in chronic HF patients, a lower level of immunoreactivity was observed compared to healthy controls (n = 13). Strong negative correlation was identified between plasma PACAP-38 and NT-proBNP levels in chronic HF, as opposed to the positive connection seen in the acute HF group. Plasma IL-1 β, IL-2 and IL-4 levels were significantly lower in chronic HF, and IL-10 was significantly higher in patients with acute HF. PACAP-38 levels of myocardial tissues were lower in all end-stage HF patients and lower PAC1 receptor levels were detected in the primary dilated cardiomyopathy group compared to the controls. We conclude that PACAP-38 and PAC1 expression correlates with some biomarkers of acute and chronic HF; therefore, further studies are necessary to explore whether PACAP could be a suitable prognostic biomarker in HF patients.
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spelling pubmed-89985042022-04-12 PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients Szabó, Dóra Sárszegi, Zsolt Polgár, Beáta Sághy, Éva Reglődi, Dóra Tóth, Tünde Onódi, Zsófia Leszek, Przemyslaw Varga, Zoltán V. Helyes, Zsuzsanna Kemény, Ágnes Ferdinandy, Péter Tamás, Andrea Int J Mol Sci Article Pituitary adenylate cyclase activating polypeptide-38 (PACAP-38) is a multifunctional neuropeptide, which may play a role in cardioprotection. However, little is known about the presence of PACAP-38 in heart failure (HF) patients. The aim of our study was to measure the alterations of PACAP-38 like immunoreactivity (LI) in acute (n = 13) and chronic HF (n = 33) and to examine potential correlations between PACAP-38 and HF predictors (cytokines, NT-proBNP). Tissue PACAP-38 LI and PAC1 receptor levels were also investigated in heart tissue samples of patients with HF. Significantly higher plasma PACAP-38 LI was detected in patients with acute HF, while in chronic HF patients, a lower level of immunoreactivity was observed compared to healthy controls (n = 13). Strong negative correlation was identified between plasma PACAP-38 and NT-proBNP levels in chronic HF, as opposed to the positive connection seen in the acute HF group. Plasma IL-1 β, IL-2 and IL-4 levels were significantly lower in chronic HF, and IL-10 was significantly higher in patients with acute HF. PACAP-38 levels of myocardial tissues were lower in all end-stage HF patients and lower PAC1 receptor levels were detected in the primary dilated cardiomyopathy group compared to the controls. We conclude that PACAP-38 and PAC1 expression correlates with some biomarkers of acute and chronic HF; therefore, further studies are necessary to explore whether PACAP could be a suitable prognostic biomarker in HF patients. MDPI 2022-03-28 /pmc/articles/PMC8998504/ /pubmed/35409075 http://dx.doi.org/10.3390/ijms23073715 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
Szabó, Dóra
Sárszegi, Zsolt
Polgár, Beáta
Sághy, Éva
Reglődi, Dóra
Tóth, Tünde
Onódi, Zsófia
Leszek, Przemyslaw
Varga, Zoltán V.
Helyes, Zsuzsanna
Kemény, Ágnes
Ferdinandy, Péter
Tamás, Andrea
PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title_full PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title_fullStr PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title_full_unstemmed PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title_short PACAP-38 and PAC1 Receptor Alterations in Plasma and Cardiac Tissue Samples of Heart Failure Patients
title_sort pacap-38 and pac1 receptor alterations in plasma and cardiac tissue samples of heart failure patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998504/
https://www.ncbi.nlm.nih.gov/pubmed/35409075
http://dx.doi.org/10.3390/ijms23073715
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