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pubmed-article:11699059pubmed:abstractTextWe demonstrate that a high-fructose diet reduces the incidence of diabetes in nonobese diabetic (NOD) mice (31.2% v 57.1% on regular chow (RC); P =.009). In a second cohort of mice, we evaluated potential mechanisms for the protective effect of the high-fructose (HF) diet and whether the metabolic changes are strain-specific. Sixty NOD and 60 Balb/c mice were randomized at weaning into HF- and RC-fed groups (30 mice each) and followed for 28 weeks. Glucose tolerance testing demonstrated improved glucose tolerance in HF diet groups (P =.001 in Balb/c; P =.04 in NOD mice at 6 months). beta-cell mass was preserved in NOD mice on the HF diet, but remained unchanged in Balb/c mice. In NOD mice, hepatic insulin receptor substrate (IRS)-2 protein expression increased by 2-fold (P =.01 for 2 v 6 months) in HF-fed mice and was 53% +/- 15% higher (P =.01) in the HF diet versus RC groups at 6 months of age. IRS-2 expression was also increased in skeletal muscle of NOD mice and in both liver and muscle of Balb/c mice. Our data suggest that a HF diet improves glucose tolerance in both NOD and Balb/c mice. The improved glucose tolerance may be related to increased IRS-2 expression and, in NOD mice, preservation of beta-cell mass.lld:pubmed
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pubmed-article:11699059pubmed:authorpubmed-author:JacksonR ARAlld:pubmed
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pubmed-article:11699059pubmed:authorpubmed-author:CordemanT PTPlld:pubmed
pubmed-article:11699059pubmed:copyrightInfoCopyright 2001 by W.B. Saunders Companylld:pubmed
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pubmed-article:11699059pubmed:volume50lld:pubmed
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pubmed-article:11699059pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:11699059pubmed:articleTitleHigh-fructose diet preserves beta-cell mass and prevents diabetes in nonobese diabetic mice: A potential role for increased insulin receptor substrate-2 expression.lld:pubmed
pubmed-article:11699059pubmed:affiliationSection on Immunology, Joslin Diabetes Center, Boston, MA 02115, USA.lld:pubmed
pubmed-article:11699059pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11699059pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:11699059pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed