Iron Regulation of Pancreatic Beta-Cell Functions and Oxidative Stress

被引:77
|
作者
Backe, Marie Balslev [1 ]
Moen, Ingrid Wahl [1 ]
Ellervik, Christina [2 ]
Hansen, Jakob Bondo [1 ]
Mandrup-Poulsen, Thomas [1 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Biomed Sci, DK-2200 Copenhagen N, Denmark
[2] Boston Childrens Hosp, Dept Lab Med, Boston, MA 02115 USA
来源
关键词
apoptosis; diabetes; insulin secretion; metal ion transport; metabolism; mitochondrial stress; reactive oxygen species; INSULIN SECRETORY CAPACITY; MITOCHONDRIAL-MEMBRANE PROTEIN; OXYGEN SPECIES PRODUCTION; ISLET B-CELLS; GLUCOSE-METABOLISM; SERUM FERRITIN; DIABETES-MELLITUS; HEREDITARY HEMOCHROMATOSIS; HYDROGEN-PEROXIDE; CHELATION-THERAPY;
D O I
10.1146/annurev-nutr-071715-050939
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Dietary advice is the cornerstone in first-line treatment of metabolic diseases. Nutritional interventions directed at these clinical conditions mainly aim to (a) improve insulin resistance by reducing energy-dense macronutrient intake to obtain weight loss and (b) reduce fluctuations in insulin secretion through avoidance of rapidly absorbable carbohydrates. However, even in the majority of motivated patients selected for clinical trials, massive efforts using this approach have failed to achieve lasting efficacy. Less attention has been given to the role of micronutrients in metabolic diseases. Here, we review the evidence that highlights (a) the importance of iron in pancreatic beta-cell function and dysfunction in diabetes and (b) the integrative pathophysiological effects of tissue iron levels in the interactions among the beta cell, gut microbiome, hypothalamus, innate and adaptive immune systems, and insulin-sensitive tissues. We propose that clinical trials are warranted to clarify the impact of dietary or pharmacological iron reduction on the development of metabolic disorders.
引用
收藏
页码:241 / 273
页数:33
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