Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation
Cardiac dysfunction is a major complication that precedes death after scorpion envenomation. Here, authors show that heart failure and mortality are caused by excessive acetylcholine release, which requires IL-1R-dependent PGE2 production. Dexamethasone treatment effectively inhibits cardiac dysfunc...
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2020-10-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-020-19232-8 |
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doaj-3824a55bb5ce42fc8ddfb1f913df0a2a2021-05-11T08:56:07ZengNature Publishing GroupNature Communications2041-17232020-10-0111111210.1038/s41467-020-19232-8Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomationMouzarllem B. Reis0Fernanda L. Rodrigues1Natalia Lautherbach2Alexandre Kanashiro3Carlos A. Sorgi4Alyne F. G. Meirelles5Carlos A. A. Silva6Karina F. Zoccal7Camila O. S. Souza8Simone G. Ramos9Alessandra K. Matsuno10Lenaldo B. Rocha11Helio C. Salgado12Luiz C. C. Navegantes13Ísis C. Kettelhut14Palmira Cupo15Luiz G. Gardinassi16Lúcia H. Faccioli17Departamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Neurociências e Ciências do Comportamento, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloCentro Universitário Barão de MauáDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloDepartamento de Patologia e Medicina Legal, Faculdade de Medicina de Ribeirão PretoDepartamento de Puericultura e Pediatria, Faculdade de Medicina de Ribeirão PretoInstituto de Ciências Biológicas e Naturais, Universidade Federal do Triângulo MineiroDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São PauloDepartamento de Puericultura e Pediatria, Faculdade de Medicina de Ribeirão PretoDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São PauloCardiac dysfunction is a major complication that precedes death after scorpion envenomation. Here, authors show that heart failure and mortality are caused by excessive acetylcholine release, which requires IL-1R-dependent PGE2 production. Dexamethasone treatment effectively inhibits cardiac dysfunction and mortality.https://doi.org/10.1038/s41467-020-19232-8 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mouzarllem B. Reis Fernanda L. Rodrigues Natalia Lautherbach Alexandre Kanashiro Carlos A. Sorgi Alyne F. G. Meirelles Carlos A. A. Silva Karina F. Zoccal Camila O. S. Souza Simone G. Ramos Alessandra K. Matsuno Lenaldo B. Rocha Helio C. Salgado Luiz C. C. Navegantes Ísis C. Kettelhut Palmira Cupo Luiz G. Gardinassi Lúcia H. Faccioli |
spellingShingle |
Mouzarllem B. Reis Fernanda L. Rodrigues Natalia Lautherbach Alexandre Kanashiro Carlos A. Sorgi Alyne F. G. Meirelles Carlos A. A. Silva Karina F. Zoccal Camila O. S. Souza Simone G. Ramos Alessandra K. Matsuno Lenaldo B. Rocha Helio C. Salgado Luiz C. C. Navegantes Ísis C. Kettelhut Palmira Cupo Luiz G. Gardinassi Lúcia H. Faccioli Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation Nature Communications |
author_facet |
Mouzarllem B. Reis Fernanda L. Rodrigues Natalia Lautherbach Alexandre Kanashiro Carlos A. Sorgi Alyne F. G. Meirelles Carlos A. A. Silva Karina F. Zoccal Camila O. S. Souza Simone G. Ramos Alessandra K. Matsuno Lenaldo B. Rocha Helio C. Salgado Luiz C. C. Navegantes Ísis C. Kettelhut Palmira Cupo Luiz G. Gardinassi Lúcia H. Faccioli |
author_sort |
Mouzarllem B. Reis |
title |
Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
title_short |
Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
title_full |
Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
title_fullStr |
Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
title_full_unstemmed |
Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
title_sort |
interleukin-1 receptor-induced pge2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2020-10-01 |
description |
Cardiac dysfunction is a major complication that precedes death after scorpion envenomation. Here, authors show that heart failure and mortality are caused by excessive acetylcholine release, which requires IL-1R-dependent PGE2 production. Dexamethasone treatment effectively inhibits cardiac dysfunction and mortality. |
url |
https://doi.org/10.1038/s41467-020-19232-8 |
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