Thiamine Deficiency: An Update of Pathophysiologic Mechanisms and Future Therapeutic Considerations

被引:83
作者
Abdou, Eman [1 ]
Hazell, Alan S. [1 ,2 ]
机构
[1] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[2] CRCHUM, NeuroRescue Lab, Montreal, PQ H2X 0A9, Canada
基金
加拿大健康研究院;
关键词
Wernicke's encephalopathy; Vitamin B-1; Stem cell; Excitotoxicity; Oxidative stress; Astrocyte; Inflammation; BLOOD-BRAIN-BARRIER; EXPERIMENTAL WERNICKES-ENCEPHALOPATHY; NEURODEGENERATIVE DISORDERS; OXIDATIVE STRESS; GLUTAMATE TRANSPORTER; ALZHEIMERS-DISEASE; DOWN-REGULATION; MITOCHONDRIAL DYSFUNCTION; HIPPOCAMPAL NEUROGENESIS; EXTRACELLULAR GLUTAMATE;
D O I
10.1007/s11064-014-1430-z
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
Thiamine is an essential vitamin that is necessary to maintain the functional integrity of cells in the brain. Its deficiency is the underlying cause of Wernicke's encephalopathy (WE), a disorder primarily associated with, but not limited to, chronic alcoholism. Thiamine deficiency leads to the development of impaired energy metabolism due to mitochondrial dysfunction in focal regions of the brain resulting in cerebral vulnerability. The consequences of this include oxidative stress, excitotoxicity, inflammatory responses, decreased neurogenesis, blood-brain barrier disruption, lactic acidosis and a reduction in astrocyte functional integrity involving a loss of glutamate transporters and other astrocyte-specific proteins which together contribute in a major way to the resulting neurodegeneration. Exactly how these factors acting in concert lead to the demise of neurons is unclear. In this review we reassess their relative importance in the light of more recent findings and discuss therapeutic possibilities that may provide hope for the future for individuals with WE.
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页码:353 / 361
页数:9
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