Modeling Molecular Pathways of Neuronal Ischemia

被引:15
|
作者
Taxin, Zachary H. [1 ]
Neymotin, Samuel A. [1 ]
Mohan, Ashutosh [1 ]
Lipton, Peter [2 ]
Lytton, William W. [1 ]
机构
[1] SUNY Downstate, Dept Physiol & Pharmacol, Brooklyn, NY 11203 USA
[2] Univ Wisconsin, Dept Neurosci, Madison, WI USA
来源
COMPUTATIONAL NEUROSCIENCE | 2014年 / 123卷
关键词
D O I
10.1016/B978-0-12-397897-4.00014-0
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
Neuronal ischemia, the consequence of a stroke (cerebrovascular accident), is a condition of reduced delivery of nutrients to brain neurons. The brain consumes more energy per gram of tissue than any other organ, making continuous blood flow critical. Loss of nutrients, most critically glucose and O-2, triggers a large number of interacting molecular pathways in neurons and astrocytes. The dynamics of these pathways take place over multiple temporal scales and occur in multiple interacting cytosolic and organelle compartments: in mitochondria, endoplasmic reticulum, and nucleus. The complexity of these relationships suggests the use of computer simulation to understand the interplay between pathways leading to reversible or irreversible damage, the forms of damage, and interventions that could reduce damage at different stages of stroke. We describe a number of models and simulation methods that can be used to further our understanding of ischemia.
引用
收藏
页码:249 / 275
页数:27
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