Brain Iron Metabolism, Redox Balance and Neurological Diseases

被引:43
作者
Gao, Guofen [1 ]
You, Linhao [1 ]
Zhang, Jianhua [1 ]
Chang, Yan-Zhong [1 ]
Yu, Peng [1 ]
机构
[1] Hebei Normal Univ, Coll Life Sci, Key Lab Anim Physiol Biochem & Mol Biol Hebei Prov, Minist Educ,Key Lab Mol & Cellular Biol, 20 Nanerhuan Eastern Rd, Shijiazhuang 050024, Peoples R China
基金
中国国家自然科学基金;
关键词
oxidative stress; Parkinson's disease; Alzheimer's disease; stroke; neurodevelopment; iron chelator; AMYLOID PRECURSOR PROTEIN; ALPHA-SYNUCLEIN PHOSPHORYLATION; DEFICIENCY ANEMIA ALTERS; DOPAMINERGIC CELL-DEATH; CENTRAL-NERVOUS-SYSTEM; GREEN TEA CATECHINS; AGE-RELATED-CHANGES; PARKINSONS-DISEASE; OXIDATIVE STRESS; ALZHEIMERS-DISEASE;
D O I
10.3390/antiox12061289
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The incidence of neurological diseases, such as Parkinson's disease, Alzheimer's disease and stroke, is increasing. An increasing number of studies have correlated these diseases with brain iron overload and the resulting oxidative damage. Brain iron deficiency has also been closely linked to neurodevelopment. These neurological disorders seriously affect the physical and mental health of patients and bring heavy economic burdens to families and society. Therefore, it is important to maintain brain iron homeostasis and to understand the mechanism of brain iron disorders affecting reactive oxygen species (ROS) balance, resulting in neural damage, cell death and, ultimately, leading to the development of disease. Evidence has shown that many therapies targeting brain iron and ROS imbalances have good preventive and therapeutic effects on neurological diseases. This review highlights the molecular mechanisms, pathogenesis and treatment strategies of brain iron metabolism disorders in neurological diseases.
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页数:34
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