Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/4032
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorFUKUDA, Thiago Y.-
dc.contributor.authorTANJI, Maury M.-
dc.contributor.authorSILVA, Suelen R.-
dc.contributor.authorSATO, Maria N.-
dc.contributor.authorPLAPLER, Helio-
dc.date.accessioned2014-01-28T22:20:31Z-
dc.date.available2014-01-28T22:20:31Z-
dc.date.issued2013-
dc.identifier.citationLASERS IN MEDICAL SCIENCE, v.28, n.5, p.1305-1313, 2013-
dc.identifier.issn0268-8921-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/4032-
dc.description.abstractTo evaluate the modulation of proinflammatory (interleukin-6, IL-6; tumor necrosis factor-alpha, TNF-alpha; and interferon-gamma, IFN-gamma) and anti-inflammatory cytokines (transforming growth factor-beta 1, TGF-beta 1) in the inflammation processes in vivo with low-level laser action, 50 isogenic mice were randomly distributed into three groups: control (no surgical procedure, n = 10), sham (surgical procedure with three standard cutaneous incisions, followed by an abdominal muscle incision and suture, n = 20), and laser (same procedure followed by laser exposure, n = 20). The sham group was divided into three subgroups: sham I (euthanasia and evaluation, 36 h after surgical procedure), sham II (euthanasia and evaluation, 60 h after surgical procedure), and sham III (euthanasia and evaluation, 84 h after surgical procedure). The laser group was also divided in three subgroups: laser I (a single laser session, 12 h after surgery), laser II (two laser sessions, 12 and 36 h after surgery), and laser III (three laser sessions, 12, 36, and 60 h after surgery). All animals in the laser groups received three points per session of continuous infrared laser (wavelength of 780 nm, power of 20 mW, fluency of 10 J/cm(2), exposure time of 20 s per point, and energy of 0.4 J). After euthanasia, spleen mononuclear cells were isolated and cultured for 48 h. Concentrations of IL-6, TNF-alpha, IFN-gamma, and TGF-beta 1 were obtained by enzyme-linked immunosorbent assay method. There was a significant difference between the IL-6 and TNF-alpha concentrations in the 60-and 84-h evaluations when the laser and sham groups were compared to the control group (p < 0.05), except for laser II in the TNF-alpha analysis (p > 0.05). The IFN-gamma concentration analysis showed a significant difference only in sham II when compared to the control group (p < 0.05). Thus, there was a modulatory effect of TNF-alpha and IFN-gamma in the laser group, particularly in the 60-h postoperative evaluation. There was no significant difference between the laser, sham, and control groups for TGF-beta 1 analysis (p > 0.05). The low-level laser application decreased the TNF-alpha and IFN-gamma release in vivo of spleen mononuclear cells in mice, especially after two exposure sessions. However, there was no modulation of the IL-6 and TGF-beta 1 release.-
dc.language.isoeng-
dc.publisherSPRINGER LONDON LTD-
dc.relation.ispartofLasers in Medical Science-
dc.rightsrestrictedAccess-
dc.subjectCytokines-
dc.subjectInflammation-
dc.subjectHealing-
dc.subjectLow-level laser therapy-
dc.subject.otherhe-ne-laser-
dc.subject.othermessenger-rna expression-
dc.subject.otherblood mononuclear-cells-
dc.subject.otherhuman peripheral-blood-
dc.subject.othertnf-alpha-
dc.subject.otherendothelial-cells-
dc.subject.otherin-vitro-
dc.subject.other650 nm-
dc.subject.otherirradiation-
dc.subject.othertherapy-
dc.titleInfrared low-level diode laser on inflammatory process modulation in mice: pro- and anti-inflammatory cytokines-
dc.typearticle-
dc.rights.holderCopyright SPRINGER LONDON LTD-
dc.identifier.doi10.1007/s10103-012-1231-z-
dc.identifier.pmid23179306-
dc.subject.wosEngineering, Biomedical-
dc.subject.wosSurgery-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalFUKUDA, Thiago Y.:Irmandade Santa Casa Misericordia Sao Paulo ISCMS, Phys Therapy Sect, Sao Paulo, Brazil; Fed Univ Sao Paulo UNIFESP, BR-04023062 Sao Paulo, Brazil-
hcfmusp.author.externalTANJI, Maury M.:FMUSP, Lab Med Invest Dermatol & Immunodeficiencies LIM, Sao Paulo, Brazil; Univ Grande ABC, Sao Paulo, Brazil-
hcfmusp.author.externalSILVA, Suelen R.:Univ Grande ABC, Sao Paulo, Brazil-
hcfmusp.author.externalPLAPLER, Helio:Fed Univ Sao Paulo UNIFESP, BR-04023062 Sao Paulo, Brazil-
hcfmusp.description.beginpage1305-
hcfmusp.description.endpage1313-
hcfmusp.description.issue5-
hcfmusp.description.volume28-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84884283261-
hcfmusp.origem.idWOS:000323742200012-
hcfmusp.publisher.cityLONDON-
hcfmusp.publisher.countryENGLAND-
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dc.description.indexMEDLINE-
hcfmusp.citation.scopus40-
hcfmusp.scopus.lastupdate2024-04-12-
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Artigos e Materiais de Revistas Científicas - FM/MDT
Departamento de Dermatologia - FM/MDT

Artigos e Materiais de Revistas Científicas - LIM/56
LIM/56 - Laboratório de Investigação em Dermatologia e Imunodeficiências


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