Continuous oral administration of atorvastatin ameliorates brain damage after transient focal ischemia in rats

被引:28
作者
Saito, Tomonari [1 ]
Nito, Chikako [1 ]
Ueda, Masayuki [1 ]
Inaba, Toshiki [1 ]
Kamiya, Fumio [1 ]
Muraga, Kanako [1 ]
Katsura, Ken-ichiro [1 ]
Katayama, Yasuo [1 ]
机构
[1] Nippon Med Sch, Grad Sch Med, Dept Neurol Sci, Tokyo 1138603, Japan
关键词
Focal cerebral ischemia; Atorvastatin; Neuroprotection; Oxidative stress; Inflammation; SPONTANEOUSLY HYPERTENSIVE-RATS; CEREBRAL-ARTERY OCCLUSION; COA REDUCTASE INHIBITOR; OXIDATIVE STRESS; BLOOD-FLOW; STROKE; MICE; INFARCTION; PROTECTS; THROMBOLYSIS;
D O I
10.1016/j.lfs.2013.11.018
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: Pre-treatment with statins is known to ameliorate ischemic brain damage after experimental stroke, and is independent of cholesterol levels. We undertook pre- vs post-ischemic treatment with atorvastatin after focal cerebral ischemia in rats. Main methods: Male Sprague-Dawley rats underwent transient 90-min middle cerebral artery occlusion (MCAO). Atorvastatin (20 mg/kg/day) or vehicle was administered orally. Rats were divided into vehicle-treated, atorvastatin pre-treatment, atorvastatin post-treatment, and atorvastatin continuous-treatment groups. In the pre-treatment, rats were given atorvastatin or vehicle for 7 days before MCAO. In the post-treatment, rats received atorvastatin or vehicle for 7 days after MCAO. Measurement of infarct volume, as well as neurological and immunohistochemical assessments, were done 24 h and 7 days after reperfusion. Key findings: Each atorvastatin-treated group demonstrated significant reductions in infarct and edema volumes compared with the vehicle-treated group 24 h after reperfusion. Seven days after reperfusion, infarct volumes in the post-treatment group and continuous-treatment group (but not the pre-treatment group) were significantly smaller than in the vehicle-treated group. Only the continuous-treatment group had significantly improved neurological scores 7 days after reperfusion compared with the vehicle group. Post-treatment and continuous-treatment groups had significantly decreased lipid peroxidation, oxidative DNA damage, microglial activation, expression of tumor necrosis factor-alpha, and neuronal damage in the cortical ischemic boundary area after 7 days of reperfusion. Significance: These results suggest that continuous oral administration (avoiding withdrawal) with statins after stroke may reduce the extent of post-ischemic brain damage and improve neurological outcome by inhibiting oxidative stress and inflammatory responses. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:106 / 114
页数:9
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