Literature DB >> 20086073

Metabolic effects of fructose and the worldwide increase in obesity.

Luc Tappy1, Kim-Anne Lê.   

Abstract

While virtually absent in our diet a few hundred years ago, fructose has now become a major constituent of our modern diet. Our main sources of fructose are sucrose from beet or cane, high fructose corn syrup, fruits, and honey. Fructose has the same chemical formula as glucose (C(6)H(12)O(6)), but its metabolism differs markedly from that of glucose due to its almost complete hepatic extraction and rapid hepatic conversion into glucose, glycogen, lactate, and fat. Fructose was initially thought to be advisable for patients with diabetes due to its low glycemic index. However, chronically high consumption of fructose in rodents leads to hepatic and extrahepatic insulin resistance, obesity, type 2 diabetes mellitus, and high blood pressure. The evidence is less compelling in humans, but high fructose intake has indeed been shown to cause dyslipidemia and to impair hepatic insulin sensitivity. Hepatic de novo lipogenesis and lipotoxicity, oxidative stress, and hyperuricemia have all been proposed as mechanisms responsible for these adverse metabolic effects of fructose. Although there is compelling evidence that very high fructose intake can have deleterious metabolic effects in humans as in rodents, the role of fructose in the development of the current epidemic of metabolic disorders remains controversial. Epidemiological studies show growing evidence that consumption of sweetened beverages (containing either sucrose or a mixture of glucose and fructose) is associated with a high energy intake, increased body weight, and the occurrence of metabolic and cardiovascular disorders. There is, however, no unequivocal evidence that fructose intake at moderate doses is directly related with adverse metabolic effects. There has also been much concern that consumption of free fructose, as provided in high fructose corn syrup, may cause more adverse effects than consumption of fructose consumed with sucrose. There is, however, no direct evidence for more serious metabolic consequences of high fructose corn syrup versus sucrose consumption.

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Year:  2010        PMID: 20086073     DOI: 10.1152/physrev.00019.2009

Source DB:  PubMed          Journal:  Physiol Rev        ISSN: 0031-9333            Impact factor:   37.312


  353 in total

1.  Fructose acutely stimulates NKCC2 activity in rat thick ascending limbs by increasing surface NKCC2 expression.

Authors:  Gustavo R Ares; Kamal M Kassem; Pablo A Ortiz
Journal:  Am J Physiol Renal Physiol       Date:  2018-12-05

2.  Sweet taste receptor signaling in beta cells mediates fructose-induced potentiation of glucose-stimulated insulin secretion.

Authors:  George A Kyriazis; Mangala M Soundarapandian; Björn Tyrberg
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-06       Impact factor: 11.205

3.  Increased hepatic de novo lipogenesis and mitochondrial efficiency in a model of obesity induced by diets rich in fructose.

Authors:  Raffaella Crescenzo; Francesca Bianco; Italia Falcone; Paola Coppola; Giovanna Liverini; Susanna Iossa
Journal:  Eur J Nutr       Date:  2012-04-28       Impact factor: 5.614

4.  Rapid increases in overweight and obesity among South African adolescents: comparison of data from the South African National Youth Risk Behaviour Survey in 2002 and 2008.

Authors:  Sasiragha P Reddy; Ken Resnicow; Shamagonam James; Itumeleng N Funani; Nilen S Kambaran; Riyadh G Omardien; Pardon Masuka; Ronel Sewpaul; Roger D Vaughan; Anthony Mbewu
Journal:  Am J Public Health       Date:  2011-11-28       Impact factor: 9.308

Review 5.  Fructose-mediated effects on gene expression and epigenetic mechanisms associated with NAFLD pathogenesis.

Authors:  Johanna K DiStefano
Journal:  Cell Mol Life Sci       Date:  2020-06       Impact factor: 9.261

6.  Vascular damage in obese female rats with hypoestrogenism.

Authors:  Luis Angel Lima-Mendoza; Juventino Colado-Velázquez; Patrick Mailloux-Salinas; Josué V Espinosa-Juárez; Norma L Gómez-Viquez; Tzindilu Molina-Muñoz; Fengyang Huang; Guadalupe Bravo
Journal:  J Physiol Biochem       Date:  2013-08-31       Impact factor: 4.158

7.  Uric acid induces hepatic steatosis by generation of mitochondrial oxidative stress: potential role in fructose-dependent and -independent fatty liver.

Authors:  Miguel A Lanaspa; Laura G Sanchez-Lozada; Yea-Jin Choi; Christina Cicerchi; Mehmet Kanbay; Carlos A Roncal-Jimenez; Takuji Ishimoto; Nanxing Li; George Marek; Murat Duranay; George Schreiner; Bernardo Rodriguez-Iturbe; Takahiko Nakagawa; Duk-Hee Kang; Yuri Y Sautin; Richard J Johnson
Journal:  J Biol Chem       Date:  2012-10-03       Impact factor: 5.157

8.  Diet high in fructose leads to an overexpression of lipocalin-2 in rat fatty liver.

Authors:  Salamah Mohammad Alwahsh; Min Xu; Hatice Ali Seyhan; Shakil Ahmad; Sabine Mihm; Giuliano Ramadori; Frank Christian Schultze
Journal:  World J Gastroenterol       Date:  2014-02-21       Impact factor: 5.742

9.  Plasminogen activator inhibitor-1, monocyte chemoattractant protein-1, e-selectin and C-reactive protein levels in response to 4-week very-high-fructose or -glucose diets.

Authors:  G Silbernagel; J Machann; H-U Häring; A Fritsche; A Peter
Journal:  Eur J Clin Nutr       Date:  2013-11-13       Impact factor: 4.016

Review 10.  Strategies in the nutritional management of gestational diabetes.

Authors:  Teri L Hernandez; Molly A Anderson; Catherine Chartier-Logan; Jacob E Friedman; Linda A Barbour
Journal:  Clin Obstet Gynecol       Date:  2013-12       Impact factor: 2.190

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