Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1
| Ano de defesa: | 2009 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso embargado |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal do Rio Grande do Norte
BR UFRN Programa de Pós-Graduação em Ciências Farmacêuticas Bioanálises e Medicamentos |
| Programa de Pós-Graduação: |
Não Informado pela instituição
|
| Departamento: |
Não Informado pela instituição
|
| País: |
Não Informado pela instituição
|
| Palavras-chave em Português: | |
| Link de acesso: | https://repositorio.ufrn.br/jspui/handle/123456789/13456 |
Resumo: | Inflammation has been pointed out as an important factor in development of chronic diseases, as diabetes. Hyperglycemia condition would be responsible by toll-like receptors, TLR2 and TLR4, and, consequently by local and systemic inflammation induction. Thus, the objective of present study was to evaluate type 1 Diabetes mellitus (T1DM) pro-inflammatory state through mRNA expression of TLRs 2 and 4 and proinflammatory cytokines IL-1β, IL-6 and TNF-α correlating to diabetic nephropathy. In order to achieve this objective, 76 T1DM patients and 100 normoglycemic (NG) subjects aged between 6 and 20 years were evaluated. T1DM subjects were evaluated as a total group DM1, and considering glycemic control (good glycemic control DM1G, and poor glycemic control DM1P) and considering time of diagnosis (before achieving 5 years of diagnosis DM1< 5yrs, and after achieving 5 years of diagnosis DM1 <5yrs). Metabolic control was evaluated by glucose and glycated hemoglobin concentrations; to assess renal function serum urea, creatinine, albumin, total protein and urinary albumin-to-creatinine ratio were determined and to evaluate hepatic function, AST and ALT serum activities were measured. Pro-inflammatory status was assessed by mRNA expression of TLRs 2 and 4 and the inflammatory cytokines IL-1β, IL-6 and TNF-α. Except for DM1G group (18.4%), DM1NC patients (81.6%) showed a poor glycemic control, with glycated hemoglobin (11,2%) and serum glucose (225,5 md/dL) concentrations significantly increased in relation to NG group (glucose: 76,5mg/dL and glycated hemoglobin: 6,9%). Significantly enhanced values of urea (20%) and ACR (20,8%) and diminished concentrations of albumin (5,7%) and total protein (13,6%) were found in T1DM patients, mainly associated to a poor glycemic control (DM1P increased values of urea: 20% and ACR:49%, and diminished of albumin: 13,6% and total protein:13,6%) and longer disease duration (DM1 <5yrs - increased values of urea: 20% and ACR:20,8%, and diminished of albumin: 14,3% and total protein:13,6%). As regarding pro-inflammatory status evaluation, significantly increased mRNA expressions were presented for TLR2 (37,5%), IL-1β (43%), IL-6 (44,4%) and TNF-α (15,6%) in T1DM patients in comparison to NG, mainly associated to DM1P (poor glycemic control TLR2: 82%, IL-1β: 36,8% increase) and DM1 <5yrs (longer time of diagnosis TLR2: 85,4%, IL-1β: 46,5% increased) groups. Results support the existence of an inflammatory state mediated by an increased expression of TLR2 and pro-inflammatory cytokines IL-1β, IL-6 and TNF-α in T1DM |
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Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1Diabetes mellitus tipo 1InflamaçãoTLR2CitocinasNefropatia diabéticaType 1 Diabetes mellitusInflammationTLR2CytokinesDiabetic nephropathyCNPQ::CIENCIAS DA SAUDE::FARMACIAInflammation has been pointed out as an important factor in development of chronic diseases, as diabetes. Hyperglycemia condition would be responsible by toll-like receptors, TLR2 and TLR4, and, consequently by local and systemic inflammation induction. Thus, the objective of present study was to evaluate type 1 Diabetes mellitus (T1DM) pro-inflammatory state through mRNA expression of TLRs 2 and 4 and proinflammatory cytokines IL-1β, IL-6 and TNF-α correlating to diabetic nephropathy. In order to achieve this objective, 76 T1DM patients and 100 normoglycemic (NG) subjects aged between 6 and 20 years were evaluated. T1DM subjects were evaluated as a total group DM1, and considering glycemic control (good glycemic control DM1G, and poor glycemic control DM1P) and considering time of diagnosis (before achieving 5 years of diagnosis DM1< 5yrs, and after achieving 5 years of diagnosis DM1 <5yrs). Metabolic control was evaluated by glucose and glycated hemoglobin concentrations; to assess renal function serum urea, creatinine, albumin, total protein and urinary albumin-to-creatinine ratio were determined and to evaluate hepatic function, AST and ALT serum activities were measured. Pro-inflammatory status was assessed by mRNA expression of TLRs 2 and 4 and the inflammatory cytokines IL-1β, IL-6 and TNF-α. Except for DM1G group (18.4%), DM1NC patients (81.6%) showed a poor glycemic control, with glycated hemoglobin (11,2%) and serum glucose (225,5 md/dL) concentrations significantly increased in relation to NG group (glucose: 76,5mg/dL and glycated hemoglobin: 6,9%). Significantly enhanced values of urea (20%) and ACR (20,8%) and diminished concentrations of albumin (5,7%) and total protein (13,6%) were found in T1DM patients, mainly associated to a poor glycemic control (DM1P increased values of urea: 20% and ACR:49%, and diminished of albumin: 13,6% and total protein:13,6%) and longer disease duration (DM1 <5yrs - increased values of urea: 20% and ACR:20,8%, and diminished of albumin: 14,3% and total protein:13,6%). As regarding pro-inflammatory status evaluation, significantly increased mRNA expressions were presented for TLR2 (37,5%), IL-1β (43%), IL-6 (44,4%) and TNF-α (15,6%) in T1DM patients in comparison to NG, mainly associated to DM1P (poor glycemic control TLR2: 82%, IL-1β: 36,8% increase) and DM1 <5yrs (longer time of diagnosis TLR2: 85,4%, IL-1β: 46,5% increased) groups. Results support the existence of an inflammatory state mediated by an increased expression of TLR2 and pro-inflammatory cytokines IL-1β, IL-6 and TNF-α in T1DMConselho Nacional de Desenvolvimento Científico e TecnológicoA inflamação tem sido descrita como um fator importante no desenvolvimento de doenças crônicas como o diabetes, e a condição da hiperglicemia seria a responsável pela ativação dos receptores toll-like (TLRs), TLR2 e TLR4, e, conseqüentemente, pela indução da inflamação local e sistêmica. Nesse sentido, o presente estudo teve como objetivo de avaliar o estado pró-inflamatório do Diabetes mellitus tipo 1 (DM1) através da expressão gênica de TLRs 2 e 4 e das citocinas pró-inflamatórias IL-1β, IL-6 e TNF- α, e correlacionar com o desenvolvimento da nefropatia diabética. Foram estudados 76 pacientes diabéticos tipo 1 e 100 indivíduos normoglicêmicos NG, na faixa etária de 6 a 20 anos. Os indivíduos diabéticos foram avaliados como um grupo total DM1, e subdivididos em função do controle glicêmico (diabéticos compensados DM1C, e não-compensados DM1NC) e em função do tempo de diagnóstico (diabéticos com menos de 5 anos de diagnóstico DM1< 5anos, e a partir de 5 anos de diagnóstico DM1 <5 anos). Para a avaliação do controle metabólico foram determinadas as concentrações de glicose e de hemoglobina glicada; para avaliar a função renal as concentrações séricas de uréia, creatinina, albumina, proteína total e a relação albumina/creatinina (RAC) urinária; e para função hepática a atividade sérica de AST e ALT. O estado pró-inflamatório foi avaliado a partir da expressão do mRNA dos TLRs 2 e 4, e das citocinas IL-1β, IL-6 e TNF-α. Com exceção do grupo DM1C (18,4%), os pacientes DM1NC (81,6%) apresentaram um controle glicêmico insatisfatório, com valores de mediana para glicose (225,5mg/dL) e hemoglobina glicada (11,2%) significativamente superiores ao grupo NG (glicose: 76,5mg/dL e hemoglobina glicada: 6,9%). Foram obtidos valores aumentados para a uréia sérica (20%) e RAC urinária (20,8%); e diminuídos para albumina (5,7%) e proteína total (13,6%) nos indivíduos diabéticos; e associados a um controle glicêmico insatisfatório (DM1NC aumento de 20% para uréia e 49% para RAC; e diminuição de 8,6% para albumina e 12,1% para proteína total) e a um maior tempo de diagnóstico (DM1 <5anos aumento de 20% para uréia e 20,8% para RAC; e diminuição de 14,3% para albumina e 13,6% para proteína total). No tocante à avaliação do estado pró-inflamatório, as expressões de mRNA se apresentaram elevadas para TLR2 (37,5%), IL-1β (43%), IL-6 (44,4%) e TNF-α (15,6%) nos indivíduos diabéticos em relação aos NG, sendo principalmente associadas aos grupos DM1NC (controle glicêmico insatisfatório TLR2: 82%, IL-1β: 43% de aumento) e DM1 <5 anos (maior tempo de diagnóstico TLR2: 85,4%, IL-1β: 46,5% de aumento). O conjunto de resultados suporta a existência de um quadro inflamatório mediado pelo aumento da expressão do TLR2 e das citocinas pró-inflamatórias IL-1β, IL-6 e TNF-α no diabetes tipo 1Universidade Federal do Rio Grande do NorteBRUFRNPrograma de Pós-Graduação em Ciências FarmacêuticasBioanálises e MedicamentosRezende, Adriana Augusto dehttp://lattes.cnpq.br/8016222352823817http://lattes.cnpq.br/4245215108740331Sales, Valéria Soraya de Fariashttp://lattes.cnpq.br/8525532896559374Hirata, Mario Hiroyukihttp://lattes.cnpq.br/8551642748793896Ururahy, Marcela Abbott Galvão2014-12-17T14:16:26Z2011-01-032014-12-17T14:16:26Z2009-03-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfapplication/pdfURURAHY, Marcela Abbott Galvão. Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1. 2009. 114 f. Dissertação (Mestrado em Bioanálises e Medicamentos) - Universidade Federal do Rio Grande do Norte, Natal, 2009.https://repositorio.ufrn.br/jspui/handle/123456789/13456porinfo:eu-repo/semantics/embargoedAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRN2019-05-26T05:22:38Zoai:repositorio.ufrn.br:123456789/13456Repositório InstitucionalPUBhttp://repositorio.ufrn.br/oai/repositorio@bczm.ufrn.bropendoar:2019-05-26T05:22:38Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
| dc.title.none.fl_str_mv |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| title |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| spellingShingle |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 Ururahy, Marcela Abbott Galvão Diabetes mellitus tipo 1 Inflamação TLR2 Citocinas Nefropatia diabética Type 1 Diabetes mellitus Inflammation TLR2 Cytokines Diabetic nephropathy CNPQ::CIENCIAS DA SAUDE::FARMACIA |
| title_short |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| title_full |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| title_fullStr |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| title_full_unstemmed |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| title_sort |
Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1 |
| author |
Ururahy, Marcela Abbott Galvão |
| author_facet |
Ururahy, Marcela Abbott Galvão |
| author_role |
author |
| dc.contributor.none.fl_str_mv |
Rezende, Adriana Augusto de http://lattes.cnpq.br/8016222352823817 http://lattes.cnpq.br/4245215108740331 Sales, Valéria Soraya de Farias http://lattes.cnpq.br/8525532896559374 Hirata, Mario Hiroyuki http://lattes.cnpq.br/8551642748793896 |
| dc.contributor.author.fl_str_mv |
Ururahy, Marcela Abbott Galvão |
| dc.subject.por.fl_str_mv |
Diabetes mellitus tipo 1 Inflamação TLR2 Citocinas Nefropatia diabética Type 1 Diabetes mellitus Inflammation TLR2 Cytokines Diabetic nephropathy CNPQ::CIENCIAS DA SAUDE::FARMACIA |
| topic |
Diabetes mellitus tipo 1 Inflamação TLR2 Citocinas Nefropatia diabética Type 1 Diabetes mellitus Inflammation TLR2 Cytokines Diabetic nephropathy CNPQ::CIENCIAS DA SAUDE::FARMACIA |
| description |
Inflammation has been pointed out as an important factor in development of chronic diseases, as diabetes. Hyperglycemia condition would be responsible by toll-like receptors, TLR2 and TLR4, and, consequently by local and systemic inflammation induction. Thus, the objective of present study was to evaluate type 1 Diabetes mellitus (T1DM) pro-inflammatory state through mRNA expression of TLRs 2 and 4 and proinflammatory cytokines IL-1β, IL-6 and TNF-α correlating to diabetic nephropathy. In order to achieve this objective, 76 T1DM patients and 100 normoglycemic (NG) subjects aged between 6 and 20 years were evaluated. T1DM subjects were evaluated as a total group DM1, and considering glycemic control (good glycemic control DM1G, and poor glycemic control DM1P) and considering time of diagnosis (before achieving 5 years of diagnosis DM1< 5yrs, and after achieving 5 years of diagnosis DM1 <5yrs). Metabolic control was evaluated by glucose and glycated hemoglobin concentrations; to assess renal function serum urea, creatinine, albumin, total protein and urinary albumin-to-creatinine ratio were determined and to evaluate hepatic function, AST and ALT serum activities were measured. Pro-inflammatory status was assessed by mRNA expression of TLRs 2 and 4 and the inflammatory cytokines IL-1β, IL-6 and TNF-α. Except for DM1G group (18.4%), DM1NC patients (81.6%) showed a poor glycemic control, with glycated hemoglobin (11,2%) and serum glucose (225,5 md/dL) concentrations significantly increased in relation to NG group (glucose: 76,5mg/dL and glycated hemoglobin: 6,9%). Significantly enhanced values of urea (20%) and ACR (20,8%) and diminished concentrations of albumin (5,7%) and total protein (13,6%) were found in T1DM patients, mainly associated to a poor glycemic control (DM1P increased values of urea: 20% and ACR:49%, and diminished of albumin: 13,6% and total protein:13,6%) and longer disease duration (DM1 <5yrs - increased values of urea: 20% and ACR:20,8%, and diminished of albumin: 14,3% and total protein:13,6%). As regarding pro-inflammatory status evaluation, significantly increased mRNA expressions were presented for TLR2 (37,5%), IL-1β (43%), IL-6 (44,4%) and TNF-α (15,6%) in T1DM patients in comparison to NG, mainly associated to DM1P (poor glycemic control TLR2: 82%, IL-1β: 36,8% increase) and DM1 <5yrs (longer time of diagnosis TLR2: 85,4%, IL-1β: 46,5% increased) groups. Results support the existence of an inflammatory state mediated by an increased expression of TLR2 and pro-inflammatory cytokines IL-1β, IL-6 and TNF-α in T1DM |
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2009 |
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2009-03-30 2011-01-03 2014-12-17T14:16:26Z 2014-12-17T14:16:26Z |
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info:eu-repo/semantics/masterThesis |
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publishedVersion |
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URURAHY, Marcela Abbott Galvão. Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1. 2009. 114 f. Dissertação (Mestrado em Bioanálises e Medicamentos) - Universidade Federal do Rio Grande do Norte, Natal, 2009. https://repositorio.ufrn.br/jspui/handle/123456789/13456 |
| identifier_str_mv |
URURAHY, Marcela Abbott Galvão. Associação do receptor toll-like 2 com o estado pró-inflamatório do diabetes tipo 1. 2009. 114 f. Dissertação (Mestrado em Bioanálises e Medicamentos) - Universidade Federal do Rio Grande do Norte, Natal, 2009. |
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