Simvastatin Therapy Prevents Brain Trauma-Induced Increases in β-Amyloid Peptide Levels

被引:64
作者
Abrahamson, Eric E. [2 ]
Ikonomovic, Milos D. [2 ,3 ]
Dixon, C. Edward [4 ]
DeKosky, Steven T. [1 ,2 ,3 ]
机构
[1] Univ Virginia, Off Dean, Sch Med, Charlottesville, VA 22908 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurol, Brain Trauma Res Ctr, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Psychiat, Brain Trauma Res Ctr, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Dept Neurosurg, Brain Trauma Res Ctr, Pittsburgh, PA 15261 USA
关键词
A REDUCTASE INHIBITORS; GENE-TARGETED MICE; SEVERE HEAD-INJURY; PRECURSOR PROTEIN; IN-VIVO; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; NEURONAL SURVIVAL; CORTICAL-NEURONS; ATORVASTATIN;
D O I
10.1002/ana.21731
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Elevations in beta-amyloid peptide (A beta) levels after traumatic brain injury (TBI) may confer risk for developing Alzheimer's disease in head trauma patients. We investigated the effects of simvastatin, a 3-hydroxy-3-methylglutaryl-CoA reductase inhibitor, on hippocampal A beta burden in a clinically relevant head injury/intervention model using mice expressing human A beta. Simvastatin therapy blunted TBI-induced increases in A beta, reduced hippocampal tissue damage and microglial activation, and improved behavioral outcome. The ability of statins to reduce post-injury A beta load and ameliorate pathological sequelae of brain injury makes them potentially effective in reducing the risk of developing Alzheimer's disease in TBI patients.
引用
收藏
页码:407 / 414
页数:8
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