Literature DB >> 3701460

Tissue distribution and excretion of copper-67 intraperitoneally administered to rats fed fructose or starch.

J Holbrook, M Fields, J C Smith, S Reiser.   

Abstract

It has been suggested that impaired gut absorption of copper is the cause of the exacerbated copper deficiency signs in rats fed fructose when compared to rats fed starch. The present study was designed to examine how rats fed fructose or starch diets, either copper-deficient or supplemented, distributed and excreted 67Cu when the isotope was administered i.p. Intraperitoneal administration was chosen in an effort to circumvent primary gut absorption as a factor in the metabolism of 67Cu. After 7 wk of dietary treatment, rats received an i.p. injection of 67Cu and were placed in metabolic cages for 4 d. Regardless of dietary carbohydrate, copper-deficient rats retained similar levels of radioactivity in various tissues and excreted similar amounts of 67Cu in feces and urine. This similarity in copper metabolism in copper-deficient rats fed either fructose or starch when the gut was circumvented for isotope administration suggests that the gut could be responsible, at least in part, for the exacerbated signs associated with the copper deficiency in rats fed fructose. The possibility is discussed that alterations in metabolism may increase the requirement for copper when fructose is the main dietary carbohydrate.

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Year:  1986        PMID: 3701460     DOI: 10.1093/jn/116.5.831

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  7 in total

1.  Uptake of radiolabeled copper from portal blood containing fructose or glucose.

Authors:  M Fields; C G Lewis; A Rose; J C Smith; S Reiser
Journal:  Biol Trace Elem Res       Date:  1986-10       Impact factor: 3.738

2.  High fructose feeding induces copper deficiency in Sprague-Dawley rats: a novel mechanism for obesity related fatty liver.

Authors:  Ming Song; Dale A Schuschke; Zhanxiang Zhou; Theresa Chen; William M Pierce; Renwei Wang; W Thomas Johnson; Craig J McClain
Journal:  J Hepatol       Date:  2011-07-23       Impact factor: 25.083

3.  Dietary fructose vs glucose lowers copper solubility in the digesta in the small intestine of rats.

Authors:  G J Van den Berg; S Yu; A Van der Heijden; A G Lemmens; A C Beynen
Journal:  Biol Trace Elem Res       Date:  1993-08       Impact factor: 3.738

4.  Dietary fructose vs glucose does not influence iron status in rats.

Authors:  A C Beynen; I A Brouwer; A G Lemmens
Journal:  Biol Trace Elem Res       Date:  1992-10       Impact factor: 3.738

Review 5.  Copper-Fructose Interactions: A Novel Mechanism in the Pathogenesis of NAFLD.

Authors:  Ming Song; Miriam B Vos; Craig J McClain
Journal:  Nutrients       Date:  2018-11-21       Impact factor: 5.717

6.  Effects of Fructose and Stress on Rat Renal Copper Metabolism and Antioxidant Enzymes Function.

Authors:  Danica Tasić; Miloš Opačić; Sanja Kovačević; Aleksandra Nikolić Kokić; Milena Dimitrijević; Dušan Nikolić; Danijela Vojnović Milutinović; Duško Blagojević; Ana Djordjevic; Jelena Brkljačić
Journal:  Int J Mol Sci       Date:  2022-08-12       Impact factor: 6.208

7.  Modest fructose beverage intake causes liver injury and fat accumulation in marginal copper deficient rats.

Authors:  Ming Song; Dale A Schuschke; Zhanxiang Zhou; Theresa Chen; Xue Shi; Jiayuan Zhang; Xiang Zhang; William M Pierce; W Thomas Johnson; Miriam B Vos; Craig J McClain
Journal:  Obesity (Silver Spring)       Date:  2013-05-31       Impact factor: 5.002

  7 in total

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