The link between iron, metabolic syndrome, and Alzheimer's disease

被引:48
作者
Gruenblatt, Edna [1 ,2 ]
Bartl, Jasmin [2 ]
Riederer, Peter [2 ]
机构
[1] Univ Zurich, Dept Child & Adolescent Psychiat, CH-8032 Zurich, Switzerland
[2] Univ Wurzburg, Natl Parkinson Fdn Ctr Excellence Labs, Neurochem Lab, Clin & Policlin Psychiat Psychosomat & Psychother, D-97080 Wurzburg, Germany
关键词
Alzheimer's disease; beta-Amyloid; Diabetes; Heme oxygenase-1; Insulin resistance; Iron; Metabolic syndrome; Metallothionein; Mitochondria; Oxidative stress; Reactive oxygen species (ROS); TYPE-2; DIABETES-MELLITUS; CEREBRAL ENERGY-METABOLISM; NEURONAL INSULIN-RECEPTOR; AMYLOID-BETA-PEPTIDES; RESISTANT BRAIN STATE; OXIDATIVE STRESS; SERUM FERRITIN; TRANSFERRIN RECEPTORS; COGNITIVE IMPAIRMENT; PANCREATIC-ISLETS;
D O I
10.1007/s00702-010-0426-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Both Alzheimer's disease (AD), the most common form of dementia, and type-2 diabetes mellitus (T2DM), a disease associated with metabolic syndrome (MetS), affect a great number of the world population and both have increased prevalence with age. Recently, many studies demonstrated that pre-diabetes, MetS, and T2DM are risk factors in the development of AD and have many common mechanisms. The main focus of studies is the insulin resistance outcome found both in MetS as well as in brains of AD subjects. However, oxidative stress (OS)-related mechanisms, which are well known to be involved in AD, including mitochondrial dysfunction, elevated iron concentration, reactive oxygen species (ROS), and stress-related enzyme or proteins (e.g. heme oxygenase-1, transferrin, etc.), have not been elucidated in MetS or T2DM brains although OS and iron are involved in the degeneration of the pancreatic islet beta cells. Therefore, this review sets to cover the current literature regarding OS and iron in MetS and T2DM and the similarities to mechanisms in AD both in human subjects as well as in animal models.
引用
收藏
页码:371 / 379
页数:9
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