Changes in the pro-inflammatory cytokine production and peritoneal macrophage function in rats with chronic heart failure

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dc.contributor.authorBatista, M. L.
dc.contributor.authorSantos, Ronaldo Vagner Thomatieli dos [UNIFESP]
dc.contributor.authorCunha, L. M.
dc.contributor.authorMattos, K.
dc.contributor.authorOliveira, E. M.
dc.contributor.authorSeelaender, M. C. L.
dc.contributor.authorRosa, L. F. B. P. Costa
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.date.accessioned2016-01-24T12:41:13Z
dc.date.available2016-01-24T12:41:13Z
dc.date.issued2006-06-01
dc.description.abstractChronic heart failure (CHF) is a state of immune activation, and pro-inflammatory cytokines play an important role in its development and progression. Macrophages (M phi s), when activated, are the main source of pro-inflammatory cytokines. We measured interjeukin-6 (IL-6), interleukin (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha) production after lipopolysaccharide (LPS)-stimulation, as well as peritoneal M phi s migration, phagocytic capacity, chemotaxis index, and hydrogen peroxide production, in an attempt to clarify the role of this cell in an animal model of CHF. Ligature of the left coronary artery or sham operation was performed in adult Wistar rats. After 12 weeks, resident and total cell number, phagocytic capacity, chemotaxis index, and hydrogen peroxide production in M phi s were significantly higher in CHF than in control rats. the production of IL-6 and TNF-alpha was similarly significantly enhanced in CHF as compared with controls. M phi s obtained from CHF rats were more responsive to LPS, suggesting the existence, in vivo, of possible factor(s) modulating the production of pro-inflammatory cytokines. the results demonstrated that there is modification of peritoneal M phi s function along CHF development, possibly contributing to the pathophysiological process in the establishment of CHF. (c) 2006 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv São Paulo, Inst Biomed Sci, Mol Biol Cell Grp, BR-05508 São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Sch Sport & Phys Educ, Dept Biodynam Human Body Movement, BR-05508 São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, Paulista Sch Med, Res Ctr Psychobiol & Sports, BR-04023062 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Paulista Sch Med, Res Ctr Psychobiol & Sports, BR-04023062 São Paulo, Brazil
dc.description.sourceWeb of Science
dc.format.extent284-290
dc.identifierhttps://dx.doi.org/10.1016/j.cyto.2006.06.004
dc.identifier.citationCytokine. London: Academic Press Ltd Elsevier B.V., v. 34, n. 5-6, p. 284-290, 2006.
dc.identifier.doi10.1016/j.cyto.2006.06.004
dc.identifier.issn1043-4666
dc.identifier.urihttps://repositorio.unifesp.br/handle/11600/28947
dc.identifier.wosWOS:000240536700007
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofCytokine
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.rights.licensehttps://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.subjectChronic heart failureen
dc.subjectPeritoneal macrophagesen
dc.subjectChemotaxisen
dc.subjectHydrogen peroxideen
dc.subjectPro-inflammatory cytokinesen
dc.titleChanges in the pro-inflammatory cytokine production and peritoneal macrophage function in rats with chronic heart failureen
dc.typeinfo:eu-repo/semantics/article
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