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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/140922
Ver los metadatos del registro completo
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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 http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://sedici.unlp.edu.ar/handle/10915/140922 |
url |
http://sedici.unlp.edu.ar/handle/10915/140922 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
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openAccess |
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http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
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application/pdf 232-240 |
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