Literature DB >> 15702436

Effects of dietary fructose on liver steatosis in overfed mule ducks.

S Davail1, N Rideau, M D Bernadet, J M André, G Guy, R Hoo-Paris.   

Abstract

Overfeeding of some waterfowl species results in obesity, which is mainly characterized by a dramatic hepatic steatosis induced by strong accumulation of lipids synthesized from dietary glucose in the liver. In mammals, fructose is known to be able to raise plasma triacylglycerol concentrations significantly; consequently, this may induce obesity. The aim of this study was to assess the effect of partial replacement of dietary glucose provided by corn starch with fructose on metabolism and fatty liver production in the Mule ducks. On the basis of 9.5 kg maize (132,920 kJ) given twice a day for 14 days, a supplementation of 9,800 kJ was provided in form of glucose, sucrose or high fructose corn syrup (HFCS: 50 % glucose, 42 % fructose and 8 % other saccharides). Fatty liver weight in ducks fed with glucose supplementation was 499 +/- 21 g. Sucrose or HFCS supplementation brought about a significant increase in liver weight (+ 18.7 % and + 16.3 % vs. glucose supplementation respectively, p < 0.05). These results suggest that the dietary fructose favors the liver steatosis by increasing hepatic lipogenesis. Postprandial plasma insulin concentrations were similar in ducks fed diets with or without fructose, suggesting that the effect of fructose on liver steatosis is not mediated by insulin.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15702436     DOI: 10.1055/s-2005-861029

Source DB:  PubMed          Journal:  Horm Metab Res        ISSN: 0018-5043            Impact factor:   2.936


  7 in total

1.  Soft drinks consumption and nonalcoholic fatty liver disease.

Authors:  William Nseir; Fares Nassar; Nimer Assy
Journal:  World J Gastroenterol       Date:  2010-06-07       Impact factor: 5.742

2.  Effects of long-term consumption of a high-fructose diet on conventional cardiovascular risk factors in Sprague-Dawley rats.

Authors:  Mohammad M Abdullah; Natalie N Riediger; Qilin Chen; Zhaohui Zhao; Nazila Azordegan; Zuyuan Xu; Gabor Fischer; Rgia A Othman; Grant N Pierce; Paramjit S Tappia; Jitao Zou; Mohammed H Moghadasian
Journal:  Mol Cell Biochem       Date:  2009-02-24       Impact factor: 3.396

3.  Soft drink consumption linked with fatty liver in the absence of traditional risk factors.

Authors:  Nimer Assy; Gattas Nasser; Iad Kamayse; William Nseir; Zaza Beniashvili; Agness Djibre; Maria Grosovski
Journal:  Can J Gastroenterol       Date:  2008-10       Impact factor: 3.522

4.  Fructose consumption as a risk factor for non-alcoholic fatty liver disease.

Authors:  Xiaosen Ouyang; Pietro Cirillo; Yuri Sautin; Shannon McCall; James L Bruchette; Anna Mae Diehl; Richard J Johnson; Manal F Abdelmalek
Journal:  J Hepatol       Date:  2008-03-10       Impact factor: 25.083

5.  Hepatic oxidative stress in fructose-induced fatty liver is not caused by sulfur amino acid insufficiency.

Authors:  Sachin S Kunde; James R Roede; Miriam B Vos; Michael L Orr; Young-Mi Go; Youngja Park; Thomas R Ziegler; Dean P Jones
Journal:  Nutrients       Date:  2011-11-18       Impact factor: 5.717

6.  Practice guidelines on NAFLD.

Authors:  Melissa Palmer
Journal:  Hepatology       Date:  2013-01-04       Impact factor: 17.425

7.  Fructose, high-fructose corn syrup, sucrose, and nonalcoholic fatty liver disease or indexes of liver health: a systematic review and meta-analysis.

Authors:  Mei Chung; Jiantao Ma; Kamal Patel; Samantha Berger; Joseph Lau; Alice H Lichtenstein
Journal:  Am J Clin Nutr       Date:  2014-08-06       Impact factor: 7.045

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.