4.5 Review

Fetal programming of glucose-insulin metabolism

期刊

MOLECULAR AND CELLULAR ENDOCRINOLOGY
卷 297, 期 1-2, 页码 4-9

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2008.06.020

关键词

Type 2 diabetes; Programming; Beta cell; Thrifty Phenotype Hypothesis; Low protein

资金

  1. Biotechnology and Biological Sciences Research Council [BB/E00797X/1] Funding Source: Medline
  2. Biotechnology and Biological Sciences Research Council [BB/E00797X/1] Funding Source: researchfish
  3. BBSRC [BB/E00797X/1] Funding Source: UKRI

向作者/读者索取更多资源

Epidemiological studies have shown a link between poor fetal growth and increased risk of developing type 2 diabetes. These observations are highly reproducible in many populations worldwide although the mechanisms behind them remain elusive. The 'Thrifty Phenotype Hypothesis' was proposed to explain the underlying causes of these relationships. Animal models of poor intrauterine nutrition have been utilised to help to define the causal factors and identify the molecular mechanisms. Programmed changes in beta cell function and insulin action have been a common feature of animal models of poor intrauterine nutrition. Fundamental underlying mechanisms are starting to emerge, including changes in the epigenotype and mitochondrial function. (C) 2008 Elsevier Ireland Ltd. All rights reserved.

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