Matches in SemOpenAlex for { <https://semopenalex.org/work/W2080841269> ?p ?o ?g. }
Showing items 1 to 98 of
98
with 100 items per page.
- W2080841269 endingPage "769" @default.
- W2080841269 startingPage "763" @default.
- W2080841269 abstract "Camundongos knouckout para o gene do receptor de lipoproteína de baixa densidade (LDLr−/−) são hiperlipidêmicos espontâneos e resistentes ao desenvolvimento de lesões neointimais. O presente estudo teve como objetivo determinar o fator que previne o processo inflamatório, as lesões neointimais cardiovasculares e a resistência insulínica nos camundongos LDLr−/−. Utilizaram-se três grupos experimentais de camundongos machos com três meses de idade: Grupo WT, camundongos selvagens; Grupo S, camundongos LDLr−/− que receberam ração padrão; Grupo HL, camundongos LDLr−/− que receberam ração hiperlipídica. Após 15 dias, o sangue foi coletado para análise plasmática dos lipídeos, glicose e insulina. O índice de Homa foi calculado para determinar a resistência à insulina. O coração e aorta foram removidos e processados histologicamente. Cortes histológicos do coração foram processados imunoistoquimicamente com anticorpo anti-CD40L para avaliar a presença de processo inflamatório. Cortes histológicos das artérias foram corados com hematoxilina/eosina e picrosírius red para avaliar alterações morfológicas e morfométricas. Os camundongos S foram resistentes ao processo inflamatório, caracterizado por baixa imunorreatividade para o CD40L, com níveis plasmáticos de HDL elevados, e não desenvolveram resistência insulínica, mesmo com hiperlipidemia moderada em relação aos WT. Os camundongos HL apresentaram uma hiperlipidemia grave, aumento na imunorreatividade cardíaca para o CD40L, pronunciadas alterações morfológicas na parede da aorta e resistência insulínica, associadas a um decréscimo nos níveis plasmáticos do HDL em relação aos S. Esta hiperlipidemia grave dos camundongos HL pode ser considerada o fator metabólico indutor do maior estresse oxidativo no sistema cardiovascular, aumentando a peroxidação lipídica da molécula de HDL e consequentemente sua remoção hepática, com consequente diminuição dos níveis plasmáticos do HDL. O nível plasmático elevado de HDL é o fator protetor contra o desenvolvimento de processos inflamatórios cardiovasculares e resistência insulínica nos camundongos LDLr−/−, impedindo o desenvolvimento das lesões neointimais. LDLr−/− mice are spontaneously hyperlipidemic and resistant to the development of neointimal lesions. This study aimed to determine the factor that prevents the inflammatory process and neointimal lesions and insulin resistance in LDLr−/− mice. Three groups of 3-month-old male mice were used: wild-type mice (WT group); LDLr−/− mice fed a standard diet (S group); and LDLr−/− mice fed a high-fat diet (HF group). After 15 days, blood was collected for analysis of plasma lipids, glucose and insulin. The HOMA index was calculated to determine insulin resistance. The heart and aorta were removed for histological study. Histological sections of the heart were processed immunohistochemically with anti-CD40L antibodies to evaluate the inflammatory process. Histological sections of the aorta were stained with hematoxylin/eosin and picrosirius red to assess morphological and morphometric alterations. The S mice were resistant to the inflammatory process, as shown by low immunoreactivity to CD40L, with high plasma HDL levels, and did not develop insulin resistance, even with moderate hyperlipidemia compared to WT. The HF mice showed severe hyperlipidemia, increased cardiac immunoreactivity to CD40L, pronounced morphological changes in the aortic wall and insulin resistance, associated with a decrease in plasma HDL levels, compared to S. This severe hyperlipidemia in the HF mice can be considered the major metabolic factor inducing oxidative stress in the cardiovascular system, increasing the lipid peroxidation of HDL and hence its removal by the liver, with consequent lowering of plasma HDL levels. High HDL plasma levels are a protective factor against the development of cardiovascular inflammation and insulin resistance in LDLr−/− mice, preventing the development of neointimal lesions." @default.
- W2080841269 created "2016-06-24" @default.
- W2080841269 creator A5000534493 @default.
- W2080841269 creator A5005123624 @default.
- W2080841269 creator A5022603485 @default.
- W2080841269 creator A5029215968 @default.
- W2080841269 creator A5031418401 @default.
- W2080841269 creator A5039550853 @default.
- W2080841269 creator A5053037711 @default.
- W2080841269 creator A5059563311 @default.
- W2080841269 creator A5075956815 @default.
- W2080841269 creator A5081499761 @default.
- W2080841269 creator A5081776374 @default.
- W2080841269 date "2011-10-01" @default.
- W2080841269 modified "2023-10-18" @default.
- W2080841269 title "Efeito anti-inflamatório da lipoproteína de alta densidade no sistema cardiovascular de camundongos hiperlipidêmicos" @default.
- W2080841269 cites W1827002599 @default.
- W2080841269 cites W1972450490 @default.
- W2080841269 cites W1976389091 @default.
- W2080841269 cites W1984194278 @default.
- W2080841269 cites W1988879418 @default.
- W2080841269 cites W1989249306 @default.
- W2080841269 cites W1990089345 @default.
- W2080841269 cites W2019904737 @default.
- W2080841269 cites W2022897423 @default.
- W2080841269 cites W2024864441 @default.
- W2080841269 cites W2038430913 @default.
- W2080841269 cites W2055502077 @default.
- W2080841269 cites W2059227051 @default.
- W2080841269 cites W2099536385 @default.
- W2080841269 cites W2107378767 @default.
- W2080841269 cites W2112187949 @default.
- W2080841269 cites W2115411470 @default.
- W2080841269 cites W2116404316 @default.
- W2080841269 cites W2120794924 @default.
- W2080841269 cites W2124091270 @default.
- W2080841269 cites W2129316761 @default.
- W2080841269 cites W2159087408 @default.
- W2080841269 cites W2163192960 @default.
- W2080841269 cites W2163289904 @default.
- W2080841269 cites W2186950905 @default.
- W2080841269 cites W2215629512 @default.
- W2080841269 cites W2285049207 @default.
- W2080841269 cites W2324841714 @default.
- W2080841269 cites W2043420525 @default.
- W2080841269 doi "https://doi.org/10.1016/s0870-2551(11)70024-5" @default.
- W2080841269 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22118127" @default.
- W2080841269 hasPublicationYear "2011" @default.
- W2080841269 type Work @default.
- W2080841269 sameAs 2080841269 @default.
- W2080841269 citedByCount "10" @default.
- W2080841269 countsByYear W20808412692015 @default.
- W2080841269 countsByYear W20808412692017 @default.
- W2080841269 countsByYear W20808412692018 @default.
- W2080841269 countsByYear W20808412692020 @default.
- W2080841269 countsByYear W20808412692021 @default.
- W2080841269 crossrefType "journal-article" @default.
- W2080841269 hasAuthorship W2080841269A5000534493 @default.
- W2080841269 hasAuthorship W2080841269A5005123624 @default.
- W2080841269 hasAuthorship W2080841269A5022603485 @default.
- W2080841269 hasAuthorship W2080841269A5029215968 @default.
- W2080841269 hasAuthorship W2080841269A5031418401 @default.
- W2080841269 hasAuthorship W2080841269A5039550853 @default.
- W2080841269 hasAuthorship W2080841269A5053037711 @default.
- W2080841269 hasAuthorship W2080841269A5059563311 @default.
- W2080841269 hasAuthorship W2080841269A5075956815 @default.
- W2080841269 hasAuthorship W2080841269A5081499761 @default.
- W2080841269 hasAuthorship W2080841269A5081776374 @default.
- W2080841269 hasBestOaLocation W20808412691 @default.
- W2080841269 hasConcept C153911025 @default.
- W2080841269 hasConcept C185592680 @default.
- W2080841269 hasConcept C86803240 @default.
- W2080841269 hasConceptScore W2080841269C153911025 @default.
- W2080841269 hasConceptScore W2080841269C185592680 @default.
- W2080841269 hasConceptScore W2080841269C86803240 @default.
- W2080841269 hasIssue "10" @default.
- W2080841269 hasLocation W20808412691 @default.
- W2080841269 hasLocation W20808412692 @default.
- W2080841269 hasLocation W20808412693 @default.
- W2080841269 hasOpenAccess W2080841269 @default.
- W2080841269 hasPrimaryLocation W20808412691 @default.
- W2080841269 hasRelatedWork W1531601525 @default.
- W2080841269 hasRelatedWork W1990781990 @default.
- W2080841269 hasRelatedWork W2319480705 @default.
- W2080841269 hasRelatedWork W2384464875 @default.
- W2080841269 hasRelatedWork W2606230654 @default.
- W2080841269 hasRelatedWork W2607424097 @default.
- W2080841269 hasRelatedWork W2748952813 @default.
- W2080841269 hasRelatedWork W2899084033 @default.
- W2080841269 hasRelatedWork W2948807893 @default.
- W2080841269 hasRelatedWork W2778153218 @default.
- W2080841269 hasVolume "30" @default.
- W2080841269 isParatext "false" @default.
- W2080841269 isRetracted "false" @default.
- W2080841269 magId "2080841269" @default.
- W2080841269 workType "article" @default.