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Mitochondria in traumatic brain injury and mitochondrial-targeted multipotential therapeutic strategies
被引:269
|作者:
Cheng, Gang
[1
]
Kong, Rong-hua
[2
]
Zhang, Lei-ming
[1
]
Zhang, Jian-ning
[1
]
机构:
[1] PLA Navy Gen Hosp, Dept Neurosurg, Beijing 100048, Peoples R China
[2] Fourth Mil Med Univ, Outpatient Dept, Xian 710032, Peoples R China
关键词:
traumatic brain injury;
mitochondrion;
mitochondrial membrane permeabilization;
apoptosis;
necrosis;
energy;
APOPTOSIS-INDUCING FACTOR;
PERMEABILITY TRANSITION PORE;
CYTOCHROME-C RELEASE;
BCL-2 FAMILY PROTEINS;
ADENINE-NUCLEOTIDE TRANSLOCATOR;
HIV PROTEASE INHIBITORS;
ACTIVATED T-LYMPHOCYTES;
DEPENDENT ANION CHANNEL;
FOCAL CEREBRAL-ISCHEMIA;
CELL-DEATH;
D O I:
10.1111/j.1476-5381.2012.02025.x
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Traumatic brain injury (TBI) is a major health and socioeconomic problem throughout the world. It is a complicated pathological process that consists of primary insults and a secondary insult characterized by a set of biochemical cascades. The imbalance between a higher energy demand for repair of cell damage and decreased energy production led by mitochondrial dysfunction aggravates cell damage. At the cellular level, the main cause of the secondary deleterious cascades is cell damage that is centred in the mitochondria. Excitotoxicity, Ca2+ overload, reactive oxygen species (ROS), Bcl-2 family, caspases and apoptosis inducing factor (AIF) are the main participants in mitochondria-centred cell damage following TBI. Some preclinical and clinical results of mitochondria-targeted therapy show promise. Mitochondria- targeted multipotential therapeutic strategies offer new hope for the successful treatment of TBI and other acute brain injuries.
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页码:699 / 719
页数:21
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