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Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients
The vasoactive intestinal peptide (VIP) expression is lower in cardiac chagasic patients and is related to worse cardiac function. The reduction of VIP in patients with Chagas disease may be a result of its enhanced degradation. To test this hypothesis, the tryptase and chymase expression was evalua...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto de Medicina Tropical
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199123/ https://www.ncbi.nlm.nih.gov/pubmed/30365640 http://dx.doi.org/10.1590/S1678-9946201860057 |
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author | Pereira, Francielle Beltrão Dutra, Walderez O. Gollob, Kenneth J. Reis, Edna Afonso de Oliveira, Ana Laura Grossi Rocha, Manoel Otávio da Costa Menezes, Cristiane Alves da Silva |
author_facet | Pereira, Francielle Beltrão Dutra, Walderez O. Gollob, Kenneth J. Reis, Edna Afonso de Oliveira, Ana Laura Grossi Rocha, Manoel Otávio da Costa Menezes, Cristiane Alves da Silva |
author_sort | Pereira, Francielle Beltrão |
collection | PubMed |
description | The vasoactive intestinal peptide (VIP) expression is lower in cardiac chagasic patients and is related to worse cardiac function. The reduction of VIP in patients with Chagas disease may be a result of its enhanced degradation. To test this hypothesis, the tryptase and chymase expression was evaluated. We also related VIP levels with interleukin-17 (IL-17) expression since VIP may modulate IL-17 production. Plasma levels of chymase were higher in chagasic patients. Conversely, VIP/chymase and VIP/tryptase ratios were lower in chagasic patients when compared to non-infected individuals. Besides, the VIP/chymase ratio was lower in chagasic cardiac patients in comparison with the indeterminate group. A positive correlation between tryptase and chymase levels was observed in chagasic cardiac patients. In relation to IL-17, we observed a higher expression of this cytokine in the cardiac form of the disease than in the indeterminate form. IL-17/VIP ratio was higher in the cardiac form in comparison with non-infected or indeterminate form. These results suggest that the low levels of VIP observed in chagasic patients could be due to an increased production of chymase and/or to the additive effect of the interaction between chymase and tryptase in the cardiac form. Moreover, the decreased VIP expression may contribute to the increase of IL-17 in chagasic cardiac patients. |
format | Online Article Text |
id | pubmed-6199123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Instituto de Medicina Tropical |
record_format | MEDLINE/PubMed |
spelling | pubmed-61991232018-10-24 Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients Pereira, Francielle Beltrão Dutra, Walderez O. Gollob, Kenneth J. Reis, Edna Afonso de Oliveira, Ana Laura Grossi Rocha, Manoel Otávio da Costa Menezes, Cristiane Alves da Silva Rev Inst Med Trop Sao Paulo Original Article The vasoactive intestinal peptide (VIP) expression is lower in cardiac chagasic patients and is related to worse cardiac function. The reduction of VIP in patients with Chagas disease may be a result of its enhanced degradation. To test this hypothesis, the tryptase and chymase expression was evaluated. We also related VIP levels with interleukin-17 (IL-17) expression since VIP may modulate IL-17 production. Plasma levels of chymase were higher in chagasic patients. Conversely, VIP/chymase and VIP/tryptase ratios were lower in chagasic patients when compared to non-infected individuals. Besides, the VIP/chymase ratio was lower in chagasic cardiac patients in comparison with the indeterminate group. A positive correlation between tryptase and chymase levels was observed in chagasic cardiac patients. In relation to IL-17, we observed a higher expression of this cytokine in the cardiac form of the disease than in the indeterminate form. IL-17/VIP ratio was higher in the cardiac form in comparison with non-infected or indeterminate form. These results suggest that the low levels of VIP observed in chagasic patients could be due to an increased production of chymase and/or to the additive effect of the interaction between chymase and tryptase in the cardiac form. Moreover, the decreased VIP expression may contribute to the increase of IL-17 in chagasic cardiac patients. Instituto de Medicina Tropical 2018-10-22 /pmc/articles/PMC6199123/ /pubmed/30365640 http://dx.doi.org/10.1590/S1678-9946201860057 Text en https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Pereira, Francielle Beltrão Dutra, Walderez O. Gollob, Kenneth J. Reis, Edna Afonso de Oliveira, Ana Laura Grossi Rocha, Manoel Otávio da Costa Menezes, Cristiane Alves da Silva Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title | Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title_full | Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title_fullStr | Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title_full_unstemmed | Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title_short | Vasoactive intestinal peptide degradation might influence Interleukin-17 expression in cardiac chagasic patients |
title_sort | vasoactive intestinal peptide degradation might influence interleukin-17 expression in cardiac chagasic patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199123/ https://www.ncbi.nlm.nih.gov/pubmed/30365640 http://dx.doi.org/10.1590/S1678-9946201860057 |
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