Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury

Autores
Stringa, Pablo Luis; Toledano, Victor; Papa-Gobbi, Rodrigo; Arreola, Miguel; Largo, Carlota; Machuca, Mariana Alejandra; Aguirre, Luis A.; Rumbo, Martín; López-Collazo, Eduardo; Hernández Oliveros, Francisco
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Background: Galactomannan (GAL), a polysaccharide present on the cell wall of several fungi, has shown an ability to modulate inflammatory responses through the dectin-1 receptor in human macrophages. However, studies evaluating the modulatory properties of this polysaccharide in in vivo inflammatory scenarios are scarce. We hypothesized that GAL pretreatment would modulate local and remote damage related to intestinal reperfusion after an ischemic insult. Materials and methods: Adult male Balb/c mice were subjected to intestinal ischemia–reperfusion injury by reversible occlusion of the superior mesenteric artery, consisting of 45 min of ischemia followed by 3 or 24 h of reperfusion. Intragastric GAL (70 mg/kg) was administered 12 h before ischemia, and saline solution was used in the control animals. Jejunum, lung, and blood samples were taken for the analysis of histology, gene expression, plasma cytokine levels, and nitrosative stress. Results: Intestinal and lung histologic alterations were attenuated by GAL pretreatment, showing significant differences compared with nontreated animals. Interleukin 1β, monocyte chemoattractant protein 1, and IL-6 messenger RNA expression were considerably downregulated in the small intestine of the GAL group. In addition, GAL treatment significantly prevented plasma interleukin 6 and monocyte chemoattractant protein 1 upregulation and diminished nitrate and nitrite levels after 3 h of intestinal reperfusion. Conclusions: GAL pretreatment constitutes a novel and promising therapy to reduce local and remote damage triggered by intestinal ischemia–reperfusion injury. Further in vivo and in vitro studies to understand GAL's modulatory effects are warranted.
Facultad de Ciencias Veterinarias
Instituto de Estudios Inmunológicos y Fisiopatológicos
Materia
Medicina
Intestine
Reperfusion injury
Mesenteric ischemia
Digestive system surgical procedures
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/140922

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spelling Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion InjuryStringa, Pablo LuisToledano, VictorPapa-Gobbi, RodrigoArreola, MiguelLargo, CarlotaMachuca, Mariana AlejandraAguirre, Luis A.Rumbo, MartínLópez-Collazo, EduardoHernández Oliveros, FranciscoMedicinaIntestineReperfusion injuryMesenteric ischemiaDigestive system surgical proceduresBackground: Galactomannan (GAL), a polysaccharide present on the cell wall of several fungi, has shown an ability to modulate inflammatory responses through the dectin-1 receptor in human macrophages. However, studies evaluating the modulatory properties of this polysaccharide in <i>in vivo</i> inflammatory scenarios are scarce. We hypothesized that GAL pretreatment would modulate local and remote damage related to intestinal reperfusion after an ischemic insult. Materials and methods: Adult male Balb/c mice were subjected to intestinal ischemia–reperfusion injury by reversible occlusion of the superior mesenteric artery, consisting of 45 min of ischemia followed by 3 or 24 h of reperfusion. Intragastric GAL (70 mg/kg) was administered 12 h before ischemia, and saline solution was used in the control animals. Jejunum, lung, and blood samples were taken for the analysis of histology, gene expression, plasma cytokine levels, and nitrosative stress. Results: Intestinal and lung histologic alterations were attenuated by GAL pretreatment, showing significant differences compared with nontreated animals. Interleukin 1β, monocyte chemoattractant protein 1, and IL-6 messenger RNA expression were considerably downregulated in the small intestine of the GAL group. In addition, GAL treatment significantly prevented plasma interleukin 6 and monocyte chemoattractant protein 1 upregulation and diminished nitrate and nitrite levels after 3 h of intestinal reperfusion. Conclusions: GAL pretreatment constitutes a novel and promising therapy to reduce local and remote damage triggered by intestinal ischemia–reperfusion injury. Further <i>in vivo</i> and <i>in vitro</i> studies to understand GAL's modulatory effects are warranted.Facultad de Ciencias VeterinariasInstituto de Estudios Inmunológicos y Fisiopatológicos2020-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf232-240http://sedici.unlp.edu.ar/handle/10915/140922enginfo:eu-repo/semantics/altIdentifier/issn/1095-8673info:eu-repo/semantics/altIdentifier/issn/0022-4804info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jss.2019.10.027info:eu-repo/semantics/altIdentifier/pmid/31796217info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T11:04:28Zoai:sedici.unlp.edu.ar:10915/140922Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 11:04:29.196SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
title Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
spellingShingle Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
Stringa, Pablo Luis
Medicina
Intestine
Reperfusion injury
Mesenteric ischemia
Digestive system surgical procedures
title_short Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
title_full Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
title_fullStr Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
title_full_unstemmed Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
title_sort Galactomannan as a Potential Modulator of Intestinal Ischemia-Reperfusion Injury
dc.creator.none.fl_str_mv Stringa, Pablo Luis
Toledano, Victor
Papa-Gobbi, Rodrigo
Arreola, Miguel
Largo, Carlota
Machuca, Mariana Alejandra
Aguirre, Luis A.
Rumbo, Martín
López-Collazo, Eduardo
Hernández Oliveros, Francisco
author Stringa, Pablo Luis
author_facet Stringa, Pablo Luis
Toledano, Victor
Papa-Gobbi, Rodrigo
Arreola, Miguel
Largo, Carlota
Machuca, Mariana Alejandra
Aguirre, Luis A.
Rumbo, Martín
López-Collazo, Eduardo
Hernández Oliveros, Francisco
author_role author
author2 Toledano, Victor
Papa-Gobbi, Rodrigo
Arreola, Miguel
Largo, Carlota
Machuca, Mariana Alejandra
Aguirre, Luis A.
Rumbo, Martín
López-Collazo, Eduardo
Hernández Oliveros, Francisco
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Medicina
Intestine
Reperfusion injury
Mesenteric ischemia
Digestive system surgical procedures
topic Medicina
Intestine
Reperfusion injury
Mesenteric ischemia
Digestive system surgical procedures
dc.description.none.fl_txt_mv Background: Galactomannan (GAL), a polysaccharide present on the cell wall of several fungi, has shown an ability to modulate inflammatory responses through the dectin-1 receptor in human macrophages. However, studies evaluating the modulatory properties of this polysaccharide in <i>in vivo</i> inflammatory scenarios are scarce. We hypothesized that GAL pretreatment would modulate local and remote damage related to intestinal reperfusion after an ischemic insult. Materials and methods: Adult male Balb/c mice were subjected to intestinal ischemia–reperfusion injury by reversible occlusion of the superior mesenteric artery, consisting of 45 min of ischemia followed by 3 or 24 h of reperfusion. Intragastric GAL (70 mg/kg) was administered 12 h before ischemia, and saline solution was used in the control animals. Jejunum, lung, and blood samples were taken for the analysis of histology, gene expression, plasma cytokine levels, and nitrosative stress. Results: Intestinal and lung histologic alterations were attenuated by GAL pretreatment, showing significant differences compared with nontreated animals. Interleukin 1β, monocyte chemoattractant protein 1, and IL-6 messenger RNA expression were considerably downregulated in the small intestine of the GAL group. In addition, GAL treatment significantly prevented plasma interleukin 6 and monocyte chemoattractant protein 1 upregulation and diminished nitrate and nitrite levels after 3 h of intestinal reperfusion. Conclusions: GAL pretreatment constitutes a novel and promising therapy to reduce local and remote damage triggered by intestinal ischemia–reperfusion injury. Further <i>in vivo</i> and <i>in vitro</i> studies to understand GAL's modulatory effects are warranted.
Facultad de Ciencias Veterinarias
Instituto de Estudios Inmunológicos y Fisiopatológicos
description Background: Galactomannan (GAL), a polysaccharide present on the cell wall of several fungi, has shown an ability to modulate inflammatory responses through the dectin-1 receptor in human macrophages. However, studies evaluating the modulatory properties of this polysaccharide in <i>in vivo</i> inflammatory scenarios are scarce. We hypothesized that GAL pretreatment would modulate local and remote damage related to intestinal reperfusion after an ischemic insult. Materials and methods: Adult male Balb/c mice were subjected to intestinal ischemia–reperfusion injury by reversible occlusion of the superior mesenteric artery, consisting of 45 min of ischemia followed by 3 or 24 h of reperfusion. Intragastric GAL (70 mg/kg) was administered 12 h before ischemia, and saline solution was used in the control animals. Jejunum, lung, and blood samples were taken for the analysis of histology, gene expression, plasma cytokine levels, and nitrosative stress. Results: Intestinal and lung histologic alterations were attenuated by GAL pretreatment, showing significant differences compared with nontreated animals. Interleukin 1β, monocyte chemoattractant protein 1, and IL-6 messenger RNA expression were considerably downregulated in the small intestine of the GAL group. In addition, GAL treatment significantly prevented plasma interleukin 6 and monocyte chemoattractant protein 1 upregulation and diminished nitrate and nitrite levels after 3 h of intestinal reperfusion. Conclusions: GAL pretreatment constitutes a novel and promising therapy to reduce local and remote damage triggered by intestinal ischemia–reperfusion injury. Further <i>in vivo</i> and <i>in vitro</i> studies to understand GAL's modulatory effects are warranted.
publishDate 2020
dc.date.none.fl_str_mv 2020-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/140922
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dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/issn/0022-4804
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jss.2019.10.027
info:eu-repo/semantics/altIdentifier/pmid/31796217
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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Creative Commons Attribution 4.0 International (CC BY 4.0)
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Creative Commons Attribution 4.0 International (CC BY 4.0)
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