Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UFPB |
Texto Completo: | https://repositorio.ufpb.br/jspui/handle/123456789/18324 |
Resumo: | Atherosclerosis is a progressive vascular inflammation, initiated by the retention of lowdensity lipoprotein (LDL), leading to oxidative stress, decrease nitric oxide (NO) bioavailability and vasodilation, increased vasoconstriction, and arterial obstruction due to the formation of atheroma plaques. Inorganic nitrates and probiotic microorganisms, from exogenous sources, have emerged as alternatives for the formation of NO, reduction in cholesterol levels, reduction of oxidative stress and reduction of atheroma plaques. Thus, pharmacological agents that are capable of improving vascular function are considered promising for combating atherosclerosis. The aim of the study was to evaluate the effects of the association of sodium nitrate (NaNO3) with Lactobacillus plantarum WJL on experimental atherosclerosis. Were used mice, male and female, from C57BL/6 and apoE-/-knockout strains for apolipoprotein E. The mice were divided into five experimental groups: c57 control (C), apoE-/- control (C), apoE-/- Nitrate (N), apoE-/- Probiotics (P) and apoE-/- association (P + N). At the end of the treatment, the animals were euthanized, the blood was collected to perform the total cholesterol test, and the aortic artery was collected for the study of vascular function and histological analysis. Vascular function was assessed by constructing concentration-response curves to acetylcholine (Ach) and also concentration-response curves to PHE. To evaluate the direct response to smooth muscle, concentration-response curves to PHE and relaxation with sodium nitroprusside (SNP) were performed. The apoE-/- C (male: 769±11; female: 816 ± 3.1) animals showed an increase of approximately nine times in cholesterol levels in relation to C57 C (male: 85±2.1; female: 76±26). The apoE-/- N (male: 679±41; fêmeas:619±92) animals showed a reduction in cholesterol levels when compared to apoE-/-C. In atherosclerotic lesions, a reduction in the formation of plaques was identified in apoE-/- P males (1.9±1.3 vs. apoE-/- C: 12±0.97).The apoE-/- C animals (males: Rmax: 91.0 ± 3.69 and EC50: 6.71 ± 0.25; females: Rmax: 83.3 ± 5.10 and EC50: 7.0 ± 0, 15) didn’t present endothelial dysfunction in relation to ACh relaxation when compared to C57 C (males Rmax: 88.8 ± 5.54 and EC50: 7.11 ± 0.12; females: Rmax: 73.2 ± 4.74 and EC50: 7.1 ± 0.27) The treated animals also didn’t present significant differences, apoE-/- P (males: Rmax: 90.2 ± 18.9 and EC50: 7.2 ± 0.24; females: Rmax : 85.9 ± 2.50 and EC50: 7.2 ± 0.29), apoE-/- N (males: Rmax: 99.5 ± 6.65 and EC50: 7.0 ± 0.12; females: Rmax: 84.8 ± 10.5 and EC50: 6.4 ± 0.22), apoE-/- P + N (males: Rmax: 81.1 ± 5.35 and EC50: 7.0 ± 0.10 ; females: Rmax: 83.6 ± 5.22 and EC50: 6.9 ± 0.23. In the PHE response curves, apoE-/- C (males: Rmax: 102 ± 1.41 and EC50: 7.3 ± 0.079; females: Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31) showed marked endothelial dysfunction with high contractile response when compared to C57 C (males: Rmax: 59.1 ± 5.39 and EC50: 7.0 ± 0.066; females: Rmax: 72.0 ± 10.3 and EC50: 7.2 ± 0.18). In males the dysfunction of the apoE-/- N animals (Rmax: 46.67 ± 4.27 and EC50: 6.7 ± 0.18) and apoE-/- P + N (Rmax: 62.2 ± 7.91 e EC50: 6.9 ± 0.048), were reversed by the treatments. In the absence of endothelium, we observed a reduction in apoE-/- N (Rmax: 90.0 ± 5.66 EC50: 7.3 ± 0.097) and apoE-/- P + N (Rmax: 105 ± 6.98 and EC50: 7.4 ± 0.04) compared to apoE-/- C (Rmax: 145 ± 8.86 and EC50: 7.7 ± 0.06). In females facing the PHE curve with functional endothelium, endothelial dysfunction was reversed in the apoE-/- P groups (Rmax: 67.2 ± 5.41 and EC50: 7.0 ± 0.13) and apoE-/- P + N (Rmax: 78.6 ± 5.05 and EC50: 7.2 ± 0.073) in relation to apoE -/- C (Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31). In the absence of endothelium, we observed an increase in sensitivity in the apoE-/- N groups (Rmax: 112 ± 7.46 and EC50: 7.9 ± 0.06) and apoE- /-P + N (Rmax: 104 ± 5.57 and EC50: 7.6 ± 0.07) compared to apoE-/- C (Rmax: 117 ± 13.3 and EC50: 6.5 ± 0.28). In response to NPS, we observed a lower sensitivity of vascular smooth muscle in apoE-/- N males (Rmax: 128 ± 12.0 and EC50: 7.6 ± 0.12 vs. apoE-/- C Rmax: 115 ± 7.5 and EC50: 8.3 ± 0.02) and apoE-/- P + N (Rmax: 138 ± 7.3 and EC50: 7.4 ± 0.08) While there were no significant differences in females, between controls C57 C (Rmax: 126 ± 5.5 and EC50: 7.4 ± 0.27) and apoE-/- C (Rmax: 133 ± 11 and EC50: 8.1 ± 0.43) and among the treated groups apoE-/- P (Rmax: 110 ± 3.5 and EC50: 7.6 ± 0.32), apoE-/- N (Rmax: 122 ± 12 and EC50: 7.2 ± 0.04) and apoE-/- N + P (Rmax: 108 ± 1.1 and EC50: 7.2 ± 0.11) in relation to apoE-/- C. It is possible to conclude that the association of NaNO3 and L. plantarum WJL reversed endothelial dysfunction in experimental atherosclerosis in both sexes. |
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Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticosDisfunção endotelialLactobacillus plantarum WJLNaNO3Endothelial dysfunctionCNPQ::CIENCIAS BIOLOGICASAtherosclerosis is a progressive vascular inflammation, initiated by the retention of lowdensity lipoprotein (LDL), leading to oxidative stress, decrease nitric oxide (NO) bioavailability and vasodilation, increased vasoconstriction, and arterial obstruction due to the formation of atheroma plaques. Inorganic nitrates and probiotic microorganisms, from exogenous sources, have emerged as alternatives for the formation of NO, reduction in cholesterol levels, reduction of oxidative stress and reduction of atheroma plaques. Thus, pharmacological agents that are capable of improving vascular function are considered promising for combating atherosclerosis. The aim of the study was to evaluate the effects of the association of sodium nitrate (NaNO3) with Lactobacillus plantarum WJL on experimental atherosclerosis. Were used mice, male and female, from C57BL/6 and apoE-/-knockout strains for apolipoprotein E. The mice were divided into five experimental groups: c57 control (C), apoE-/- control (C), apoE-/- Nitrate (N), apoE-/- Probiotics (P) and apoE-/- association (P + N). At the end of the treatment, the animals were euthanized, the blood was collected to perform the total cholesterol test, and the aortic artery was collected for the study of vascular function and histological analysis. Vascular function was assessed by constructing concentration-response curves to acetylcholine (Ach) and also concentration-response curves to PHE. To evaluate the direct response to smooth muscle, concentration-response curves to PHE and relaxation with sodium nitroprusside (SNP) were performed. The apoE-/- C (male: 769±11; female: 816 ± 3.1) animals showed an increase of approximately nine times in cholesterol levels in relation to C57 C (male: 85±2.1; female: 76±26). The apoE-/- N (male: 679±41; fêmeas:619±92) animals showed a reduction in cholesterol levels when compared to apoE-/-C. In atherosclerotic lesions, a reduction in the formation of plaques was identified in apoE-/- P males (1.9±1.3 vs. apoE-/- C: 12±0.97).The apoE-/- C animals (males: Rmax: 91.0 ± 3.69 and EC50: 6.71 ± 0.25; females: Rmax: 83.3 ± 5.10 and EC50: 7.0 ± 0, 15) didn’t present endothelial dysfunction in relation to ACh relaxation when compared to C57 C (males Rmax: 88.8 ± 5.54 and EC50: 7.11 ± 0.12; females: Rmax: 73.2 ± 4.74 and EC50: 7.1 ± 0.27) The treated animals also didn’t present significant differences, apoE-/- P (males: Rmax: 90.2 ± 18.9 and EC50: 7.2 ± 0.24; females: Rmax : 85.9 ± 2.50 and EC50: 7.2 ± 0.29), apoE-/- N (males: Rmax: 99.5 ± 6.65 and EC50: 7.0 ± 0.12; females: Rmax: 84.8 ± 10.5 and EC50: 6.4 ± 0.22), apoE-/- P + N (males: Rmax: 81.1 ± 5.35 and EC50: 7.0 ± 0.10 ; females: Rmax: 83.6 ± 5.22 and EC50: 6.9 ± 0.23. In the PHE response curves, apoE-/- C (males: Rmax: 102 ± 1.41 and EC50: 7.3 ± 0.079; females: Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31) showed marked endothelial dysfunction with high contractile response when compared to C57 C (males: Rmax: 59.1 ± 5.39 and EC50: 7.0 ± 0.066; females: Rmax: 72.0 ± 10.3 and EC50: 7.2 ± 0.18). In males the dysfunction of the apoE-/- N animals (Rmax: 46.67 ± 4.27 and EC50: 6.7 ± 0.18) and apoE-/- P + N (Rmax: 62.2 ± 7.91 e EC50: 6.9 ± 0.048), were reversed by the treatments. In the absence of endothelium, we observed a reduction in apoE-/- N (Rmax: 90.0 ± 5.66 EC50: 7.3 ± 0.097) and apoE-/- P + N (Rmax: 105 ± 6.98 and EC50: 7.4 ± 0.04) compared to apoE-/- C (Rmax: 145 ± 8.86 and EC50: 7.7 ± 0.06). In females facing the PHE curve with functional endothelium, endothelial dysfunction was reversed in the apoE-/- P groups (Rmax: 67.2 ± 5.41 and EC50: 7.0 ± 0.13) and apoE-/- P + N (Rmax: 78.6 ± 5.05 and EC50: 7.2 ± 0.073) in relation to apoE -/- C (Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31). In the absence of endothelium, we observed an increase in sensitivity in the apoE-/- N groups (Rmax: 112 ± 7.46 and EC50: 7.9 ± 0.06) and apoE- /-P + N (Rmax: 104 ± 5.57 and EC50: 7.6 ± 0.07) compared to apoE-/- C (Rmax: 117 ± 13.3 and EC50: 6.5 ± 0.28). In response to NPS, we observed a lower sensitivity of vascular smooth muscle in apoE-/- N males (Rmax: 128 ± 12.0 and EC50: 7.6 ± 0.12 vs. apoE-/- C Rmax: 115 ± 7.5 and EC50: 8.3 ± 0.02) and apoE-/- P + N (Rmax: 138 ± 7.3 and EC50: 7.4 ± 0.08) While there were no significant differences in females, between controls C57 C (Rmax: 126 ± 5.5 and EC50: 7.4 ± 0.27) and apoE-/- C (Rmax: 133 ± 11 and EC50: 8.1 ± 0.43) and among the treated groups apoE-/- P (Rmax: 110 ± 3.5 and EC50: 7.6 ± 0.32), apoE-/- N (Rmax: 122 ± 12 and EC50: 7.2 ± 0.04) and apoE-/- N + P (Rmax: 108 ± 1.1 and EC50: 7.2 ± 0.11) in relation to apoE-/- C. It is possible to conclude that the association of NaNO3 and L. plantarum WJL reversed endothelial dysfunction in experimental atherosclerosis in both sexes.NenhumaA aterosclerose é uma inflamação progressiva vascular, iniciada pela retenção de lipoproteína de baixa densidade (LDL), levando a um estresse oxidativo, redução na biodisponibilidade de óxido nítrico (NO) e da vasodilatação, aumento da vasoconstrição e obstrução arterial devido à formação de placas de ateroma. Nitratos inorgânicos e microrganismos probióticos, provenientes de fontes exógenas, surgiram como alternativas para a formação de NO, redução nos níveis de colesterol, diminuição do estresse oxidativo e redução das placas de ateroma. Deste modo, agentes farmacológicos que sejam capazes de melhorar a função vascular são considerados promissores para o combate à aterosclerose. O objetivo do estudo foi avaliar os efeitos da associação de nitrato de sódio (NaNO3) com Lactobacillus plantarum WJL na aterosclerose experimental. Foram utilizados camundongos, machos e fêmeas, das linhagens C57BL/6 e apoE-/- knockout para apolipoproteína E. Os camundongos foram divididos em cinco grupos experimentais: C57 controle negativo (c57C), apoE-/- controle positivo (apoE-/- C), apoE-/- nitrato (apoE-/-N), apoE-/- probióticos (apoE-/- P) e apoE-/- associação (P+N). Ao final do tratamento, os animais foram submetidos à eutanásia, o sangue foi coletado para a realização do teste de colesterol total, e a artéria aorta foi coletada para o estudo da função vascular e da análise histológica. A função vascular foi avaliada por meio da construção de curvas concentração-resposta à acetilcolina (ACh) e também curvas concentração-resposta à FEN. Para avaliar a resposta direta no músculo liso foram realizadas curvas concentração-resposta frente à FEN e posteriormente relaxamento com nitroprussiato de sódio (NPS). Os animais apoE-/-C (machos: 769±11; fêmeas: 816 ± 3,1) apresentaram incremento de aproximadamente nove vezes nos níveis de colesterol em relação ao C57 C (machos: 85±2,1; fêmeas: 76±2,6). Os animais apoE-/- N (machos 679±41; fêmeas: 619±92), apresentaram redução nos níveis de colesterol quando comparados ao apoE-/- C. Nas lesões ateroscleróticas foi identificada uma redução na formação de placas nos machos apoE-/- P (machos: 1,9±1,3 vs. apoE-/- C: 12±0,97). Os animais apoE-/- C (machos: Rmáx: 91,0 ± 3,69 e EC50: 6,71±0,25; fêmeas: Rmáx: 83,3 ± 5,10 e EC50: 7,0 ± 0,15) não apresentaram disfunção endotelial frente ao relaxamento à ACh quando comparados aos C57 C (machos Rmáx: 88,8 ± 5,54 e EC50: 7,11 ± 0,12; fêmeas: Rmáx: 73,2 ± 4,74 e EC50: 7,1 ± 0,27) Os animais tratados também não apresentaram diferenças significativas, apoE-/-P (machos: Rmáx: 90,2 ±18,9 e EC50: 7,2±0,24; fêmeas: Rmáx: 85,9 ±2,50 e EC50: 7,2±0,29), apoE-/- N (machos: Rmáx: 99,5 ±6,65 e EC50: 7,0±0,12; fêmeas: Rmáx: 84,8±10,5 e EC50: 6,4±0,22), apoE-/- P + N (machos: Rmáx: 81,1 ±5,35 e EC50: 7,0±0,10; fêmeas: Rmáx: 83,6±5,22 e EC50: 6,9±0,23. Já nas curvas resposta à FEN, os apoE-/- C (machos: Rmáx: 102±1,41 e EC50: 7,3±0,079; fêmeas: Rmáx: 101±6,10 e EC50: 6,6±0,31) demonstraram marcante disfunção endotelial com elevada resposta contrátil quando comparados aos C57 C (machos: Rmáx: 59,1±5,39 e EC50: 7,0±0,066; fêmeas: Rmáx: 72,0±10,3 e EC50: 7,2±0,18). Nos machos a disfunção dos animais apoE-/- N (Rmáx: 46,67±4,27e EC50: 6,7±0,18) e apoE-/- P + N (Rmáx: 62,2 ± 7,91e EC50: 6,9±0,048), foram revertidas pelos tratamentos. Já na ausência de endotélio, observamos redução nos apoE-/- N (Rmáx: 90,0 ±5,66 EC50: 7,3±0,097) e apoE-/- P + N (Rmáx: 105± 6,98 e EC50: 7,4±0,04) em comparação ao apoE-/-C Rmáx: 145±8,86 e EC50: 7,7±0,06). Nas fêmeas frente a curva de FEN com endotélio funcional, a disfunção endotelial foi revertida nos grupos apoE- /- P (Rmáx: 67,2±5,41 e EC50: 7,0 ±0,13) e apoE-/- P + N (Rmáx: 78,6±5,05 e EC50: 7,2±0,073) em relação ao apoE-/- C (Rmáx: 101±6,10 e EC50: 6,6±0,31). Já na ausência de endotélio, observamos aumento na sensibilidade nos grupos apoE-/- N ( Rmáx: 112 ±7,46 e EC50: 7,9±0,06) e apoE-/- P + N ( Rmáx: 104± 5,57 e EC50: 7,6±0,07) em comparação com o apoE-/- C (Rmáx: 117±13,3 e EC50: 6,5 ±0,28). Na resposta ao NPS, observamos menor sensibilidade do músculo liso vascular, nos machos apoE-/- N (Rmáx: 128±12 e EC50: 7,6±0,12 vs. apoE-/- C Rmáx: 115 ± 7,5 e EC50: 8,3±0,02) e nos apoE-/- P + N (Rmáx: 138 ± 7,3 e EC50: 7,4±0,08). Enquanto nas fêmeas não foram observadas diferenças significativas, entre os controles C57 C (Rmáx:126±5,5 e EC50: 7,4±0,27) e apoE-/-C (Rmáx: 133±11 e EC50: 8,1±0,43), e entre os grupos tratados apoE-/- P (Rmáx: 110±3,5 e EC50: 7,6±0,32), apoE-/-N (Rmáx: 122±12 e EC50: 7,2±0,04) e apoE-/- N+P (Rmáx: 108±1.1 e EC50: 7,2±0,11) em relação ao apoE-/-C. .É possível concluir que a associação de NaNO3 e L. plantarum WJL reverteu a disfunção endotelial na aterosclerose experimental em ambos os sexos.Universidade Federal da ParaíbaBrasilBiotecnologiaPrograma de Pós-Graduação em BiotecnologiaUFPBBraga, Valdir de Andradehttp://lattes.cnpq.br/0052252490653096Vidal, Ivynna Suellen Justino2020-11-01T01:20:48Z2020-04-162020-11-01T01:20:48Z2020-02-21info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesishttps://repositorio.ufpb.br/jspui/handle/123456789/18324porhttp://creativecommons.org/licenses/by-nd/3.0/br/info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFPBinstname:Universidade Federal da Paraíba (UFPB)instacron:UFPB2021-09-14T19:33:18Zoai:repositorio.ufpb.br:123456789/18324Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufpb.br/PUBhttp://tede.biblioteca.ufpb.br:8080/oai/requestdiretoria@ufpb.br|| diretoria@ufpb.bropendoar:2021-09-14T19:33:18Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB)false |
dc.title.none.fl_str_mv |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
title |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
spellingShingle |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos Vidal, Ivynna Suellen Justino Disfunção endotelial Lactobacillus plantarum WJL NaNO3 Endothelial dysfunction CNPQ::CIENCIAS BIOLOGICAS |
title_short |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
title_full |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
title_fullStr |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
title_full_unstemmed |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
title_sort |
Tratamento da aterosclerose em camundongos knockout para apolipoproteína E: associação de um doador de óxido nítrico e probióticos |
author |
Vidal, Ivynna Suellen Justino |
author_facet |
Vidal, Ivynna Suellen Justino |
author_role |
author |
dc.contributor.none.fl_str_mv |
Braga, Valdir de Andrade http://lattes.cnpq.br/0052252490653096 |
dc.contributor.author.fl_str_mv |
Vidal, Ivynna Suellen Justino |
dc.subject.por.fl_str_mv |
Disfunção endotelial Lactobacillus plantarum WJL NaNO3 Endothelial dysfunction CNPQ::CIENCIAS BIOLOGICAS |
topic |
Disfunção endotelial Lactobacillus plantarum WJL NaNO3 Endothelial dysfunction CNPQ::CIENCIAS BIOLOGICAS |
description |
Atherosclerosis is a progressive vascular inflammation, initiated by the retention of lowdensity lipoprotein (LDL), leading to oxidative stress, decrease nitric oxide (NO) bioavailability and vasodilation, increased vasoconstriction, and arterial obstruction due to the formation of atheroma plaques. Inorganic nitrates and probiotic microorganisms, from exogenous sources, have emerged as alternatives for the formation of NO, reduction in cholesterol levels, reduction of oxidative stress and reduction of atheroma plaques. Thus, pharmacological agents that are capable of improving vascular function are considered promising for combating atherosclerosis. The aim of the study was to evaluate the effects of the association of sodium nitrate (NaNO3) with Lactobacillus plantarum WJL on experimental atherosclerosis. Were used mice, male and female, from C57BL/6 and apoE-/-knockout strains for apolipoprotein E. The mice were divided into five experimental groups: c57 control (C), apoE-/- control (C), apoE-/- Nitrate (N), apoE-/- Probiotics (P) and apoE-/- association (P + N). At the end of the treatment, the animals were euthanized, the blood was collected to perform the total cholesterol test, and the aortic artery was collected for the study of vascular function and histological analysis. Vascular function was assessed by constructing concentration-response curves to acetylcholine (Ach) and also concentration-response curves to PHE. To evaluate the direct response to smooth muscle, concentration-response curves to PHE and relaxation with sodium nitroprusside (SNP) were performed. The apoE-/- C (male: 769±11; female: 816 ± 3.1) animals showed an increase of approximately nine times in cholesterol levels in relation to C57 C (male: 85±2.1; female: 76±26). The apoE-/- N (male: 679±41; fêmeas:619±92) animals showed a reduction in cholesterol levels when compared to apoE-/-C. In atherosclerotic lesions, a reduction in the formation of plaques was identified in apoE-/- P males (1.9±1.3 vs. apoE-/- C: 12±0.97).The apoE-/- C animals (males: Rmax: 91.0 ± 3.69 and EC50: 6.71 ± 0.25; females: Rmax: 83.3 ± 5.10 and EC50: 7.0 ± 0, 15) didn’t present endothelial dysfunction in relation to ACh relaxation when compared to C57 C (males Rmax: 88.8 ± 5.54 and EC50: 7.11 ± 0.12; females: Rmax: 73.2 ± 4.74 and EC50: 7.1 ± 0.27) The treated animals also didn’t present significant differences, apoE-/- P (males: Rmax: 90.2 ± 18.9 and EC50: 7.2 ± 0.24; females: Rmax : 85.9 ± 2.50 and EC50: 7.2 ± 0.29), apoE-/- N (males: Rmax: 99.5 ± 6.65 and EC50: 7.0 ± 0.12; females: Rmax: 84.8 ± 10.5 and EC50: 6.4 ± 0.22), apoE-/- P + N (males: Rmax: 81.1 ± 5.35 and EC50: 7.0 ± 0.10 ; females: Rmax: 83.6 ± 5.22 and EC50: 6.9 ± 0.23. In the PHE response curves, apoE-/- C (males: Rmax: 102 ± 1.41 and EC50: 7.3 ± 0.079; females: Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31) showed marked endothelial dysfunction with high contractile response when compared to C57 C (males: Rmax: 59.1 ± 5.39 and EC50: 7.0 ± 0.066; females: Rmax: 72.0 ± 10.3 and EC50: 7.2 ± 0.18). In males the dysfunction of the apoE-/- N animals (Rmax: 46.67 ± 4.27 and EC50: 6.7 ± 0.18) and apoE-/- P + N (Rmax: 62.2 ± 7.91 e EC50: 6.9 ± 0.048), were reversed by the treatments. In the absence of endothelium, we observed a reduction in apoE-/- N (Rmax: 90.0 ± 5.66 EC50: 7.3 ± 0.097) and apoE-/- P + N (Rmax: 105 ± 6.98 and EC50: 7.4 ± 0.04) compared to apoE-/- C (Rmax: 145 ± 8.86 and EC50: 7.7 ± 0.06). In females facing the PHE curve with functional endothelium, endothelial dysfunction was reversed in the apoE-/- P groups (Rmax: 67.2 ± 5.41 and EC50: 7.0 ± 0.13) and apoE-/- P + N (Rmax: 78.6 ± 5.05 and EC50: 7.2 ± 0.073) in relation to apoE -/- C (Rmax: 101 ± 6.10 and EC50: 6.6 ± 0.31). In the absence of endothelium, we observed an increase in sensitivity in the apoE-/- N groups (Rmax: 112 ± 7.46 and EC50: 7.9 ± 0.06) and apoE- /-P + N (Rmax: 104 ± 5.57 and EC50: 7.6 ± 0.07) compared to apoE-/- C (Rmax: 117 ± 13.3 and EC50: 6.5 ± 0.28). In response to NPS, we observed a lower sensitivity of vascular smooth muscle in apoE-/- N males (Rmax: 128 ± 12.0 and EC50: 7.6 ± 0.12 vs. apoE-/- C Rmax: 115 ± 7.5 and EC50: 8.3 ± 0.02) and apoE-/- P + N (Rmax: 138 ± 7.3 and EC50: 7.4 ± 0.08) While there were no significant differences in females, between controls C57 C (Rmax: 126 ± 5.5 and EC50: 7.4 ± 0.27) and apoE-/- C (Rmax: 133 ± 11 and EC50: 8.1 ± 0.43) and among the treated groups apoE-/- P (Rmax: 110 ± 3.5 and EC50: 7.6 ± 0.32), apoE-/- N (Rmax: 122 ± 12 and EC50: 7.2 ± 0.04) and apoE-/- N + P (Rmax: 108 ± 1.1 and EC50: 7.2 ± 0.11) in relation to apoE-/- C. It is possible to conclude that the association of NaNO3 and L. plantarum WJL reversed endothelial dysfunction in experimental atherosclerosis in both sexes. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-11-01T01:20:48Z 2020-04-16 2020-11-01T01:20:48Z 2020-02-21 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufpb.br/jspui/handle/123456789/18324 |
url |
https://repositorio.ufpb.br/jspui/handle/123456789/18324 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nd/3.0/br/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nd/3.0/br/ |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Universidade Federal da Paraíba Brasil Biotecnologia Programa de Pós-Graduação em Biotecnologia UFPB |
publisher.none.fl_str_mv |
Universidade Federal da Paraíba Brasil Biotecnologia Programa de Pós-Graduação em Biotecnologia UFPB |
dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da UFPB instname:Universidade Federal da Paraíba (UFPB) instacron:UFPB |
instname_str |
Universidade Federal da Paraíba (UFPB) |
instacron_str |
UFPB |
institution |
UFPB |
reponame_str |
Biblioteca Digital de Teses e Dissertações da UFPB |
collection |
Biblioteca Digital de Teses e Dissertações da UFPB |
repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB) |
repository.mail.fl_str_mv |
diretoria@ufpb.br|| diretoria@ufpb.br |
_version_ |
1801842961451843584 |