VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages

The spontaneous non obese diabetic (NOD) mouse model of Sjögren's syndrome provides a valuable tool to study the onset and progression of both autoimmune response and secretory dysfunction. Vasoactive intestinal peptide (VIP) is a neuro and immunopeptide with prosecretory effect in salivary gla...

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Autores principales: Larocca, Luciana, Calafat, Mario José, Roca, Valeria Inés, Franchi, Ana María, Pérez Leirós, Claudia
Publicado: 2007
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VIP
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15675769_v7_n10_p1343_Larocca
http://hdl.handle.net/20.500.12110/paper_15675769_v7_n10_p1343_Larocca
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spelling paper:paper_15675769_v7_n10_p1343_Larocca2023-06-08T16:24:08Z VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages Larocca, Luciana Calafat, Mario José Roca, Valeria Inés Franchi, Ana María Pérez Leirós, Claudia IL-10 Macrophages Nitric oxide NOD mice PGE2 VIP interleukin 10 interleukin 10 antibody interleukin 12 lipopolysaccharide monoclonal antibody nitric oxide nitrite prostaglandin E2 prostaglandin synthase tumor necrosis factor alpha vasoactive intestinal polypeptide animal cell animal experiment animal model antiinflammatory activity article autoimmune disease cell secretion controlled study cytokine production drug mechanism female immunopharmacology mouse nonhuman nonobese diabetic mouse peritoneum macrophage priority journal salivary gland Sjoegren syndrome Animals Anti-Inflammatory Agents Dinoprostone Female Interferon Type II Interleukin-10 Interleukin-12 Lipopolysaccharides Macrophages, Peritoneal Mice Mice, Inbred BALB C Mice, Inbred NOD Nitric Oxide Nitrites Vasoactive Intestinal Peptide The spontaneous non obese diabetic (NOD) mouse model of Sjögren's syndrome provides a valuable tool to study the onset and progression of both autoimmune response and secretory dysfunction. Vasoactive intestinal peptide (VIP) is a neuro and immunopeptide with prosecretory effect in salivary glands and anti-inflammatory actions in various models of autoimmune disease. Our purpose was to analyze the response of peritoneal macrophages to an inflammatory stimulus during the decline of salivary secretion in NOD mice and the potential anti-inflammatory effect of VIP. We present evidence of an increased nitric oxide production by peritoneal macrophages of NOD mice in basal and lipopolysaccharide (LPS) + IFN-γ-stimulated conditions and a lower IL-10 response to LPS compared with normal BALB/c mice. VIP inhibited LPS-induced TNF-α, IL-12 and nitrites accumulation in NOD macrophages while it increased IL-10 production. VIP effect was prevented by an anti-IL-10 monoclonal antibody and it showed an additive effect on exogenously added IL-10 only in NOD mice. The inhibitory effect of VIP-induced IL-10 on nitrites was mediated by COX metabolites mostly in NOD cells as indomethacine inhibited both the increase in IL-10 and the reduction of nitrites exerted by VIP. We conclude that both PGE2 and VIP inhibit nitric oxide production and increase IL-10 induced by LPS in NOD macrophages and VIP effect is mediated through an increase of COX metabolites and IL-10. © 2007 Elsevier B.V. All rights reserved. Fil:Larocca, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Calafat, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Roca, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Franchi, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Leirós, C.P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2007 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15675769_v7_n10_p1343_Larocca http://hdl.handle.net/20.500.12110/paper_15675769_v7_n10_p1343_Larocca
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic IL-10
Macrophages
Nitric oxide
NOD mice
PGE2
VIP
interleukin 10
interleukin 10 antibody
interleukin 12
lipopolysaccharide
monoclonal antibody
nitric oxide
nitrite
prostaglandin E2
prostaglandin synthase
tumor necrosis factor alpha
vasoactive intestinal polypeptide
animal cell
animal experiment
animal model
antiinflammatory activity
article
autoimmune disease
cell secretion
controlled study
cytokine production
drug mechanism
female
immunopharmacology
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
salivary gland
Sjoegren syndrome
Animals
Anti-Inflammatory Agents
Dinoprostone
Female
Interferon Type II
Interleukin-10
Interleukin-12
Lipopolysaccharides
Macrophages, Peritoneal
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Nitric Oxide
Nitrites
Vasoactive Intestinal Peptide
spellingShingle IL-10
Macrophages
Nitric oxide
NOD mice
PGE2
VIP
interleukin 10
interleukin 10 antibody
interleukin 12
lipopolysaccharide
monoclonal antibody
nitric oxide
nitrite
prostaglandin E2
prostaglandin synthase
tumor necrosis factor alpha
vasoactive intestinal polypeptide
animal cell
animal experiment
animal model
antiinflammatory activity
article
autoimmune disease
cell secretion
controlled study
cytokine production
drug mechanism
female
immunopharmacology
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
salivary gland
Sjoegren syndrome
Animals
Anti-Inflammatory Agents
Dinoprostone
Female
Interferon Type II
Interleukin-10
Interleukin-12
Lipopolysaccharides
Macrophages, Peritoneal
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Nitric Oxide
Nitrites
Vasoactive Intestinal Peptide
Larocca, Luciana
Calafat, Mario José
Roca, Valeria Inés
Franchi, Ana María
Pérez Leirós, Claudia
VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
topic_facet IL-10
Macrophages
Nitric oxide
NOD mice
PGE2
VIP
interleukin 10
interleukin 10 antibody
interleukin 12
lipopolysaccharide
monoclonal antibody
nitric oxide
nitrite
prostaglandin E2
prostaglandin synthase
tumor necrosis factor alpha
vasoactive intestinal polypeptide
animal cell
animal experiment
animal model
antiinflammatory activity
article
autoimmune disease
cell secretion
controlled study
cytokine production
drug mechanism
female
immunopharmacology
mouse
nonhuman
nonobese diabetic mouse
peritoneum macrophage
priority journal
salivary gland
Sjoegren syndrome
Animals
Anti-Inflammatory Agents
Dinoprostone
Female
Interferon Type II
Interleukin-10
Interleukin-12
Lipopolysaccharides
Macrophages, Peritoneal
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Nitric Oxide
Nitrites
Vasoactive Intestinal Peptide
description The spontaneous non obese diabetic (NOD) mouse model of Sjögren's syndrome provides a valuable tool to study the onset and progression of both autoimmune response and secretory dysfunction. Vasoactive intestinal peptide (VIP) is a neuro and immunopeptide with prosecretory effect in salivary glands and anti-inflammatory actions in various models of autoimmune disease. Our purpose was to analyze the response of peritoneal macrophages to an inflammatory stimulus during the decline of salivary secretion in NOD mice and the potential anti-inflammatory effect of VIP. We present evidence of an increased nitric oxide production by peritoneal macrophages of NOD mice in basal and lipopolysaccharide (LPS) + IFN-γ-stimulated conditions and a lower IL-10 response to LPS compared with normal BALB/c mice. VIP inhibited LPS-induced TNF-α, IL-12 and nitrites accumulation in NOD macrophages while it increased IL-10 production. VIP effect was prevented by an anti-IL-10 monoclonal antibody and it showed an additive effect on exogenously added IL-10 only in NOD mice. The inhibitory effect of VIP-induced IL-10 on nitrites was mediated by COX metabolites mostly in NOD cells as indomethacine inhibited both the increase in IL-10 and the reduction of nitrites exerted by VIP. We conclude that both PGE2 and VIP inhibit nitric oxide production and increase IL-10 induced by LPS in NOD macrophages and VIP effect is mediated through an increase of COX metabolites and IL-10. © 2007 Elsevier B.V. All rights reserved.
author Larocca, Luciana
Calafat, Mario José
Roca, Valeria Inés
Franchi, Ana María
Pérez Leirós, Claudia
author_facet Larocca, Luciana
Calafat, Mario José
Roca, Valeria Inés
Franchi, Ana María
Pérez Leirós, Claudia
author_sort Larocca, Luciana
title VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
title_short VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
title_full VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
title_fullStr VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
title_full_unstemmed VIP limits LPS-induced nitric oxide production through IL-10 in NOD mice macrophages
title_sort vip limits lps-induced nitric oxide production through il-10 in nod mice macrophages
publishDate 2007
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15675769_v7_n10_p1343_Larocca
http://hdl.handle.net/20.500.12110/paper_15675769_v7_n10_p1343_Larocca
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