Cellular and Molecular Neurobiology of Brain Preconditioning

被引:46
作者
Cadet, Jean Lud [1 ]
Krasnova, Irina N. [1 ]
机构
[1] NIDA, Mol Neuropsychiat Res Branch, Intramural Res Program, NIH,DHHS, Baltimore, MD 21224 USA
关键词
Neuronal degeneration; Ischemia; Stroke; Tolerance; Brain preconditioning; OXYGEN-GLUCOSE DEPRIVATION; DELAYED NEURONAL DEATH; NERVE GROWTH-FACTOR; FOCAL CEREBRAL-ISCHEMIA; ELEMENT-BINDING PROTEIN; TRANSIENT GLOBAL-ISCHEMIA; HIPPOCAMPAL CA1 REGION; RAT CORTICAL-NEURONS; INDUCIBLE FACTOR-I; MEDIATED AKT1 ACTIVATION;
D O I
10.1007/s12035-009-8051-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The tolerant brain which is a consequence of adaptation to repeated nonlethal insults is accompanied by the upregulation of protective mechanisms and the downregulation of prodegenerative pathways. During the past 20 years, evidence has accumulated to suggest that protective mechanisms include increased production of chaperones, trophic factors, and other antiapoptotic proteins. In contrast, preconditioning can cause substantial dampening of the organism's metabolic state and decreased expression of proapoptotic proteins. Recent microarray analyses have also helped to document a role of several molecular pathways in the induction of the brain refractory state. The present review highlights some of these findings and suggests that a better understanding of these mechanisms will inform treatment of a number of neuropsychiatric disorders.
引用
收藏
页码:50 / 61
页数:12
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