| Texto completo | |
| Autor(es): |
Gaisler-Silva, Fernanda
;
Cruz Junho, Carolina Victoria
;
Fredo-da-Costa, Izabelle
;
Christoffolete, Marcelo Augusto
;
Carneiro-Ramos, Marcela Sorelli
Número total de Autores: 5
|
| Tipo de documento: | Artigo Científico |
| Fonte: | CURRENT MOLECULAR MEDICINE; v. 22, n. 4, p. 9-pg., 2022-01-01. |
| Resumo | |
Background: Cardiovascular diseases correspond to the highest risk of sudden death worldwide, and obesity is largely related to be an increased risk factor. There is a higher prevalence of arterial hypertension in obese individuals, including the presence of cardiac hypertrophy. It is already known the role of toll-like receptors [TLR], mainly 2 and 4 in heart cells, as fundamental to the process of cardiac hypertrophy. Obesity has been studied as an activator of damage-associated molecular patterns [DAMPs], which use the TLR signaling pathway to increase the nuclear factor of inflammation, NF-kB, increasing cytokine expression in heart tissue. It's already known that FVB/N and C57BL/6 mouse strains have different behaviors in relation to metabolism, but the difference in cardiac tropism and innate immune system modulation are not clear. Methods: The present study aimed to evaluate the contribution of innate immune factors to cardiac hypertrophy induced by an experimental model of obesity comparing two mouse strains: C57BL/6 and FVB/N. Both strains were submitted to a high-fat diet containing 23% protein, 35.5% carbohydrate, and 35.9% fat for 68 days. Hearts were collected, weighed, and submitted to RT-qPCR, and the serum was analyzed by Bioplex. Results: We observed an increase in heart mass after 68 days in both strains. This was followed by an increase of alpha-actin only in C57BL/6 while ANF was increased in FVB/N. Gene expression of innate immune components and inflammatory cytokines were only increased in C57BL/6, but not in FVB/N. Conclusion: Based on the results obtained, we verified that C57BL/6 mice had a more robust action of innate immune system then FVB/N. (AU) | |
| Processo FAPESP: | 15/02052-3 - Estudo do papel do receptor TrkB no desenvolvimento de doença hepática gordurosa não alcoólica (DHGNA) em camundongos |
| Beneficiário: | Marcelo Augusto Christoffolete |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 15/19107-5 - TLR4 e sistema complemento: possível mecanismo chave na resposta hipertrófica do tecido cardíaco em quadro inflamatório sistêmico induzido por lesão isquêmica renal |
| Beneficiário: | Marcela Sorelli Carneiro Ramos |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 18/07811-8 - Estudo do papel da susceptibilidade ao desenvolvimento de doença hepática gordurosa não alcoólica (DHGNA) dependente do receptor neurotrophic tyrosine receptor kinase 2 truncado (Ntrk2.T1) em fígado de Camundongos C57Bl/6J superexpressando o receptor e em animais FVB/N knock-down condicional para o mesmo receptor |
| Beneficiário: | Marcelo Augusto Christoffolete |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 19/11077-0 - Alterações cardíacas induzidas por modelos de inflamação renal: participação do eixo Klotho/FGF-23 |
| Beneficiário: | Marcela Sorelli Carneiro Ramos |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |