Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation

Detalhes bibliográficos
Autor(a) principal: Barbosa,C.R.
Data de Publicação: 2007
Outros Autores: Albuquerque,E.M.V., Faria,E.C., Oliveira,H.C.F., Castilho,L.N.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Medical and Biological Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2007000300007
Resumo: The metabolic effects of carbohydrate supplementation in mice have not been extensively studied. In rats, glucose- and fructose-rich diets induce hypertriacylglycerolemia. In the present study, we compared the metabolic responses to two monosaccharide supplementations in two murine models. Adult male Wistar rats (N = 80) and C57BL/6 mice (N = 60), after 3 weeks on a standardized diet, were submitted to dietary supplementation by gavage with glucose (G) or fructose (F) solutions (500 g/L), 8 g/kg body weight for 21 days. Glycemia was significantly higher in rats after fructose treatment (F: 7.9 vs 9.3 mM) and in mice (G: 6.5 vs 10 and F: 6.6 vs 8.9 mM) after both carbohydrate treatments. Triacylglycerolemia increased significantly 1.5 times in rats after G or F supplementation. Total cholesterol did not change with G treatment in rats, but did decrease after F supplementation (1.5 vs 1.4 mM, P < 0.05). Both supplementations in rats induced insulin resistance, as suggested by the higher Homeostasis Model Assessment Index. In contrast, mice showed significant decreases in triacylglycerol (G: 1.8 vs 1.4 and F: 1.9 vs 1.4 mM, P < 0.01) and total cholesterol levels (G and F: 2.7 vs 2.5 mM, P < 0.05) after both monosaccharide supplementations. Wistar rats and C57BL/6 mice, although belonging to the same family (Muridae), presented opposite responses to glucose and fructose supplementation regarding serum triacylglycerol, free fatty acids, and insulin levels after monosaccharide treatment. Thus, while Wistar rats developed features of plurimetabolic syndrome, C57BL/6 mice presented changes in serum biochemical profile considered to be healthier for the cardiovascular system.
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spelling Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementationGlucose or fructose supplementationTriacylglycerolemiaInsulin resistanceC57BL/6 miceWistar ratsThe metabolic effects of carbohydrate supplementation in mice have not been extensively studied. In rats, glucose- and fructose-rich diets induce hypertriacylglycerolemia. In the present study, we compared the metabolic responses to two monosaccharide supplementations in two murine models. Adult male Wistar rats (N = 80) and C57BL/6 mice (N = 60), after 3 weeks on a standardized diet, were submitted to dietary supplementation by gavage with glucose (G) or fructose (F) solutions (500 g/L), 8 g/kg body weight for 21 days. Glycemia was significantly higher in rats after fructose treatment (F: 7.9 vs 9.3 mM) and in mice (G: 6.5 vs 10 and F: 6.6 vs 8.9 mM) after both carbohydrate treatments. Triacylglycerolemia increased significantly 1.5 times in rats after G or F supplementation. Total cholesterol did not change with G treatment in rats, but did decrease after F supplementation (1.5 vs 1.4 mM, P < 0.05). Both supplementations in rats induced insulin resistance, as suggested by the higher Homeostasis Model Assessment Index. In contrast, mice showed significant decreases in triacylglycerol (G: 1.8 vs 1.4 and F: 1.9 vs 1.4 mM, P < 0.01) and total cholesterol levels (G and F: 2.7 vs 2.5 mM, P < 0.05) after both monosaccharide supplementations. Wistar rats and C57BL/6 mice, although belonging to the same family (Muridae), presented opposite responses to glucose and fructose supplementation regarding serum triacylglycerol, free fatty acids, and insulin levels after monosaccharide treatment. Thus, while Wistar rats developed features of plurimetabolic syndrome, C57BL/6 mice presented changes in serum biochemical profile considered to be healthier for the cardiovascular system.Associação Brasileira de Divulgação Científica2007-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2007000300007Brazilian Journal of Medical and Biological Research v.40 n.3 2007reponame:Brazilian Journal of Medical and Biological Researchinstname:Associação Brasileira de Divulgação Científica (ABDC)instacron:ABDC10.1590/S0100-879X2007000300007info:eu-repo/semantics/openAccessBarbosa,C.R.Albuquerque,E.M.V.Faria,E.C.Oliveira,H.C.F.Castilho,L.N.eng2008-02-12T00:00:00Zoai:scielo:S0100-879X2007000300007Revistahttps://www.bjournal.org/https://old.scielo.br/oai/scielo-oai.phpbjournal@terra.com.br||bjournal@terra.com.br1414-431X0100-879Xopendoar:2008-02-12T00:00Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)false
dc.title.none.fl_str_mv Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
title Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
spellingShingle Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
Barbosa,C.R.
Glucose or fructose supplementation
Triacylglycerolemia
Insulin resistance
C57BL/6 mice
Wistar rats
title_short Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
title_full Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
title_fullStr Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
title_full_unstemmed Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
title_sort Opposite lipemic response of Wistar rats and C57BL/6 mice to dietary glucose or fructose supplementation
author Barbosa,C.R.
author_facet Barbosa,C.R.
Albuquerque,E.M.V.
Faria,E.C.
Oliveira,H.C.F.
Castilho,L.N.
author_role author
author2 Albuquerque,E.M.V.
Faria,E.C.
Oliveira,H.C.F.
Castilho,L.N.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Barbosa,C.R.
Albuquerque,E.M.V.
Faria,E.C.
Oliveira,H.C.F.
Castilho,L.N.
dc.subject.por.fl_str_mv Glucose or fructose supplementation
Triacylglycerolemia
Insulin resistance
C57BL/6 mice
Wistar rats
topic Glucose or fructose supplementation
Triacylglycerolemia
Insulin resistance
C57BL/6 mice
Wistar rats
description The metabolic effects of carbohydrate supplementation in mice have not been extensively studied. In rats, glucose- and fructose-rich diets induce hypertriacylglycerolemia. In the present study, we compared the metabolic responses to two monosaccharide supplementations in two murine models. Adult male Wistar rats (N = 80) and C57BL/6 mice (N = 60), after 3 weeks on a standardized diet, were submitted to dietary supplementation by gavage with glucose (G) or fructose (F) solutions (500 g/L), 8 g/kg body weight for 21 days. Glycemia was significantly higher in rats after fructose treatment (F: 7.9 vs 9.3 mM) and in mice (G: 6.5 vs 10 and F: 6.6 vs 8.9 mM) after both carbohydrate treatments. Triacylglycerolemia increased significantly 1.5 times in rats after G or F supplementation. Total cholesterol did not change with G treatment in rats, but did decrease after F supplementation (1.5 vs 1.4 mM, P < 0.05). Both supplementations in rats induced insulin resistance, as suggested by the higher Homeostasis Model Assessment Index. In contrast, mice showed significant decreases in triacylglycerol (G: 1.8 vs 1.4 and F: 1.9 vs 1.4 mM, P < 0.01) and total cholesterol levels (G and F: 2.7 vs 2.5 mM, P < 0.05) after both monosaccharide supplementations. Wistar rats and C57BL/6 mice, although belonging to the same family (Muridae), presented opposite responses to glucose and fructose supplementation regarding serum triacylglycerol, free fatty acids, and insulin levels after monosaccharide treatment. Thus, while Wistar rats developed features of plurimetabolic syndrome, C57BL/6 mice presented changes in serum biochemical profile considered to be healthier for the cardiovascular system.
publishDate 2007
dc.date.none.fl_str_mv 2007-03-01
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dc.relation.none.fl_str_mv 10.1590/S0100-879X2007000300007
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dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv Brazilian Journal of Medical and Biological Research v.40 n.3 2007
reponame:Brazilian Journal of Medical and Biological Research
instname:Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
instname_str Associação Brasileira de Divulgação Científica (ABDC)
instacron_str ABDC
institution ABDC
reponame_str Brazilian Journal of Medical and Biological Research
collection Brazilian Journal of Medical and Biological Research
repository.name.fl_str_mv Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)
repository.mail.fl_str_mv bjournal@terra.com.br||bjournal@terra.com.br
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