High Fat Programming of β-Cell Failure

被引:26
作者
Cerf, Marlon E. [1 ]
机构
[1] MRC, ZA-7505 Cape Town, South Africa
来源
ISLETS OF LANGERHANS | 2010年 / 654卷
关键词
Glucolipotoxicity; Nutrition; Pancreas; Type; 2; diabetes; BODY-MASS INDEX; INSULIN-RESISTANCE; DEVELOPMENTAL ORIGINS; METABOLIC SYNDROME; GLUCOSE-TOLERANCE; PANCREATIC-ISLETS; PSAMMOMYS-OBESUS; PROTEIN-DIET; MALONYL-COA; RAT ISLETS;
D O I
10.1007/978-90-481-3271-3_5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
High saturated fat intake contributes to insulin resistance, beta-cell failure, and type 2 diabetes. Developmental programming refers to a stimulus or insult during critical periods of life which includes fetal and subsequent early neonatal life. Programming alters offspring physiology and metabolism with both immediate and lasting consequences. Maternal nutrition in gestation and lactation shapes offspring development and health. A high saturated fat diet ingested by mothers during gestation and/or lactation is a form of nutritional insult that induces diabetogenic changes in offspring physiology and metabolism. High fat programming is induced by maternal high saturated fat intake during defined periods of gestation and/or lactation and programs the physiology and metabolism of the offspring in early life. This more recently adopted form of developmental programming reflects society in both affluent and developing countries. High fat programming induces adverse changes in beta-cell development and function in neonatal and weanling offspring. These changes are characterized by compromised beta-cell development and function, evident by altered expression of key factors that maintain the beta-cell phenotype. High fat programming is likely to result in beta-cell failure and eventual type 2 diabetes.
引用
收藏
页码:77 / 89
页数:13
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