4.5 Article

Prevention of Diabetes in db/db Mice by Dietary Soy Is Independent of Isoflavone Levels

Journal

ENDOCRINOLOGY
Volume 153, Issue 11, Pages 5200-5211

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1210/en.2012-1490

Keywords

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Funding

  1. Swiss Commission for Technology and Innovation and Amazentis SA [10272.1 PFLS-LS]
  2. Foundation Gertrude von Meissner
  3. Sir Jules Thorn Charitable Overseas Trust Reg., Schaan
  4. Ernst & Lucie Schmidheiny Foundation
  5. Swiss National Science Foundation [310030-135727/1]
  6. Swiss National Science Foundation (SNF) [310030_135727] Funding Source: Swiss National Science Foundation (SNF)

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Recent evidence points towards the beneficial use of soy proteins and isoflavones to improve glucose control and slow the progression of type 2 diabetes. Here, we used diabetic db/db mice fed a high soy-containing diet (SD) or a casein soy-free diet to investigate the metabolic effects of soy and isoflavones consumption on glucose homeostasis, hepatic glucose production, and pancreatic islet function. Male db/db mice fed with a SDexhibited a robust reduction in hyperglycemia (50%), correlating with a reduction in hepatic glucose production and preserved pancreatic beta-cell function. The rapid decrease in fasting glucose levels resulted from an inhibition of gluconeogenesis and an increase in glycolysis in the liver of db/db mice. Soy consumption also prevented the loss of pancreatic beta-cell massandthus improved glucose-stimulated insulin secretion (3-fold), which partly accounted for the overall improvements in glucose homeostasis. Comparison of SD effects on hyperglycemia with differing levels of isoflavones or with purified isoflavones indicate that the beneficial physiological effects of soy are not related to differences in their isoflavone content. Overall, these findings suggest that consumption of soy is beneficial for improving glucose homeostasis and delaying the progression of diabetes in the db/db mice but act independently of isoflavone concentration. (Endocrinology 153: 5200-5211, 2012)

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