Atorvastatin reduction of intracranial hematoma volume in rats subjected to controlled cortical impact

被引:43
作者
Lu, DY
Mahmood, A
Qu, CS
Goussev, A
Lu, M
Chopp, M
机构
[1] Henry Ford Hlth Sci Ctr, Dept Neurosurg, Detroit, MI USA
[2] Henry Ford Hlth Sci Ctr, Dept Biostat, Detroit, MI USA
[3] Henry Ford Hlth Sci Ctr, Dept Neurol, Detroit, MI USA
[4] Oakland Univ, Dept Phys, Rochester, MI USA
关键词
traumatic brain injury; hematoma; atorvastatin; rat;
D O I
10.3171/jns.2004.101.5.0822
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Atorvastatin, a beta-hydroxy-beta-methylglutaryl coenzyme A reductase inhibitor, has pleiotropic effects such as improving thrombogenic profile, promoting angiogenesis, and reducing inflammatory responses and has shown promise in enhancing neurological functional improvement and promoting neuroplasticity in animal models of traumatic brain injury (TBI), stroke, and intracranial hemorrhage. The authors tested the effect of atorvastatin on intracranial hematoma after TBI. Methods. Mate Wistar rats were subjected to controlled cortical impact, and atorvastatin (1 mg/kg) was orally administered 1 day after TBI and daily for 7 days thereafter. Rats were killed at 1, 8, and 15 days post-TBI. The temporal profile of intraparenchymal hematoma was measured on brain tissue sections by using a MicroComputer Imaging Device and light microscopy. Conclusions. Data in this study showed that intraparenchymal and intraventricular hemorrhages are present 1 day after TBI and are absorbed at 15 days after TBI. Furthermore, atorvastatin reduces the volume of intracranial hematoma 8 days after TBI.
引用
收藏
页码:822 / 825
页数:4
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