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Publicação:
Relationship between innate immune response toll-like receptor 4 (Tlr-4) and the pathophysiological process of obesity cardiomyopathy

dc.contributor.authorRizzi Alves, Pedro Henrique [UNESP]
dc.contributor.authorTogneri Ferron, Artur Junio [UNESP]
dc.contributor.authorCosta, Mariane Róvero [UNESP]
dc.contributor.authorHasimoto, Fabiana Kurokawa [UNESP]
dc.contributor.authorGregolin, Cristina Schmitt [UNESP]
dc.contributor.authorGarcia, Jéssica Leite [UNESP]
dc.contributor.authorDe Campos, Dijon Henrique Salomé [UNESP]
dc.contributor.authorCicogna, Antônio Carlos [UNESP]
dc.contributor.authorDe Mattei, Letícia [UNESP]
dc.contributor.authorMoreto, Fernando [UNESP]
dc.contributor.authorZanati Bazan, Silméia Garcia [UNESP]
dc.contributor.authorFrancisqueti-Ferron, Fabiane Valentini [UNESP]
dc.contributor.authorCorrêa, Camila Renata [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Mato Grosso
dc.date.accessioned2022-05-01T08:15:18Z
dc.date.available2022-05-01T08:15:18Z
dc.date.issued2021-01-01
dc.description.abstractBackground: Obesity is a chronic low-grade inflammation condition related to cardiac disorders. However, the mechanism responsible for obesity-related cardiac inflammation is unclear. The toll-like receptor 4 (TLR-4) belongs to a receptor of the transmembrane family responsible for the immune response whose activation stimulates the production of proinflammatory cytokines. Objective: To test whether the activation of the TLR-4 receptor participates in the obesity cardiomyopathy process, due to cytokine production through NF-ĸB activation. Methods: Male Wistar rats were randomized into two groups: The control group (C, n= 8 animals) that received standard diet/water and the obese group (OB, n= 8 animals) that were fed a high sugar-fat diet and water plus 25% of sucrose for 30 weeks. Nutritional analysis: Body weight, adiposity index, food, water, and caloric intake. Obesity-related disorders analysis: Plasma glucose, uric acid and triglycerides, HOMA-IR, systolic blood pressure, TNF-α in adipose tissue. Cardiac analysis included: TLR-4 and NF-ĸB protein expression, TNF-α and IL-6 levels. Comparison by unpaired Student’s t-test or Mann- Whitney test with a p-value < 0.05 as statistically significant. Results: The OB group showed obesity, high glucose, triglycerides, uric acid, HOMA, systolic blood pressure, and TNF-α in adipose tissue. OB group presented cardiac remodeling and diastolic dysfunction. TLR-4 and NF-ĸB expression and cytokine levels were higher in OB. Conclusion: Our findings conclude that, in an obesogenic condition, the inflammation derived from cardiac TLR-4 activation can be a mechanism able to lead to remodeling and cardiac dysfunction.en
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho Câmpus de Botucatu Faculdade de Medicina
dc.description.affiliationUniversidade Federal de Mato Grosso
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho Câmpus de Botucatu Faculdade de Medicina
dc.format.extent91-99
dc.identifierhttp://dx.doi.org/10.36660/abc.20190788
dc.identifier.citationArquivos Brasileiros de Cardiologia, v. 117, n. 1, p. 91-99, 2021.
dc.identifier.doi10.36660/abc.20190788
dc.identifier.issn1678-4170
dc.identifier.issn0066-782X
dc.identifier.scopus2-s2.0-85112622482
dc.identifier.urihttp://hdl.handle.net/11449/233402
dc.language.isoeng
dc.relation.ispartofArquivos Brasileiros de Cardiologia
dc.sourceScopus
dc.subjectAdipocytes
dc.subjectCardiovascular Diseases/physiopathology
dc.subjectCytokines
dc.subjectFatty Acid synthases
dc.subjectInflammation
dc.subjectNutrional Assessment
dc.subjectObesity
dc.titleRelationship between innate immune response toll-like receptor 4 (Tlr-4) and the pathophysiological process of obesity cardiomyopathyen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0001-7089-3033[2]
unesp.author.orcid0000-0002-3670-243X[6]
unesp.author.orcid0000-0002-4933-0604[7]
unesp.author.orcid0000-0002-0607-8189[11]
unesp.author.orcid0000-0003-2910-4308[12]
unesp.author.orcid0000-0001-8493-5329[13]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt

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