Effect of olmesartan and pravastatin on experimental cerebral aneurysms in rats

被引:32
作者
Kimura, Naoto [1 ,2 ]
Shimizu, Hiroaki [1 ,2 ]
Eldawoody, Hany [1 ,2 ,3 ]
Nakayama, Toshio [4 ]
Saito, Atsushi [1 ]
Tominaga, Teiji [1 ]
Takahashi, Akira [2 ,4 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Neurosurg, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Neuroendovasc Therapy, Sendai, Miyagi 9808574, Japan
[3] Mansoura Univ, Dept Neurosurg, Mansoura, Egypt
[4] Tohoku Univ, Grad Sch Biomed Engn, Dept Reconstruct Endovasc Therapy, Sendai, Miyagi 980, Japan
关键词
Cerebral aneurysm; Experimental; Olmesartan; Pravastatin; Rat; NITRIC-OXIDE BIOAVAILABILITY; RENIN-ANGIOTENSIN SYSTEM; A REDUCTASE INHIBITOR; CASE-FATALITY RATES; SUBARACHNOID HEMORRHAGE; KAPPA-B; HYPERTENSIVE-RATS; RECEPTOR BLOCKER; PROGRESSION; EXPRESSION;
D O I
10.1016/j.brainres.2010.01.044
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The major initiation process of intracranial aneurysms is thought to involve endothelial dysfunction due to hemodynamic stress. Angiotensin II type 1 receptor blockers and statins improve vascular endothelium function. The effects of olmesartan and pravastatin were investigated on the development of experimental aneurysms in rats. Eighty-three rats underwent aneurysm induction. Seven groups of 10-14 rats were treated with low or high dose olmesartan, low or high dose pravastatin, low doses of olmesartan and pravastatin, hydralazine, or no drug (control) for 12 weeks, when rats were sacrificed for vascular corrosion casting and scanning electron microscopy. Aneurysmal changes at the anterior cerebral-olfactory artery bifurcation were divided into stages 0 (no abnormality) to III (saccular aneurysm). Systolic arterial blood pressure was elevated over 170 mm Hg in the control, low dose pravastatin, and high dose pravastatin groups, but not in the other groups. The control group demonstrated aneurysmal changes in 100% and stage III in 50% of rats. Aneurysmal changes were observed in most rats in the other groups, but the incidence of stage III was 10% or less. The staging pattern showed significant differences between the groups (P=0.028). Pravastatin reduced both stages III and II + III and olmesartan ameliorated stage III, implying that these may prevent aneurysmal formation through acting on different steps. (209 words) (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:144 / 152
页数:9
相关论文
共 48 条
[1]   Simvastatin suppresses the progression of experimentally induced cerebral aneurysms in rats [J].
Aoki, Tomohiro ;
Kataoka, Hiroharu ;
Ishibashi, Ryota ;
Nozaki, Kazuhiko ;
Hashimoto, Nobuo .
STROKE, 2008, 39 (04) :1276-1285
[2]   NF-κB is a key mediator of cerebral aneurysm formation [J].
Aoki, Tomohiro ;
Kataoka, Hiroharu ;
Shimamura, Munehisa ;
Nakagami, Hironori ;
Wakayama, Kouji ;
Moriwaki, Takuya ;
Ishibashi, Ryota ;
Nozaki, Kazuhiko ;
Morishita, Ryuichi ;
Hashimoto, Nobuo .
CIRCULATION, 2007, 116 (24) :2830-2840
[3]   Macrophage-derived matrix metalloproteinase-2 and-9 promote the progression of cerebral aneurysms in rats [J].
Aoki, Tomohiro ;
Kataoka, Hiroharu ;
Morimoto, Masafumi ;
Nozaki, Kazuhiko ;
Hashimoto, Nobuo .
STROKE, 2007, 38 (01) :162-169
[4]   Role of angiotensin II type 1 receptor in cerebral aneurysm formation in rats [J].
Aoki, Tomohiro ;
Nishimura, Masaki ;
Kataoka, Hiroharu ;
Ishibashi, Ryota ;
Miyake, Takashi ;
Takagi, Yasushi ;
Morishita, Ryuichi ;
Hashimoto, Nobuo .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2009, 24 (03) :353-359
[5]   Reactive oxygen species modulate growth of cerebral aneurysms: a study using the free radical scavenger edaravone and p47phox-/- mice [J].
Aoki, Tomohiro ;
Nishimura, Masaki ;
Kataoka, Hiroharu ;
Ishibashi, Ryota ;
Nozaki, Kazuhiko ;
Hashimoto, Nobuo .
LABORATORY INVESTIGATION, 2009, 89 (07) :730-741
[6]   Impact of Monocyte Chemoattractant Protein-1 Deficiency on Cerebral Aneurysm Formation [J].
Aoki, Tomohiro ;
Kataoka, Hiroharu ;
Ishibashi, Ryota ;
Nozaki, Kazuhiko ;
Egashira, Kensuke ;
Hashimoto, Nobuo .
STROKE, 2009, 40 (03) :942-951
[7]   PITAVASTATIN SUPPRESSES FORMATION AND PROGRESSION OF CEREBRAL ANEURYSMS THROUGH INHIBITION OF THE NUCLEAR FACTOR κB PATHWAY [J].
Aoki, Tomohiro ;
Kataoka, Hiroharu ;
Ishibashi, Ryota ;
Nakagami, Hironori ;
Nozaki, Kazuhiko ;
Morishita, Ryuuichi ;
Hashimoto, Nobuo .
NEUROSURGERY, 2009, 64 (02) :357-365
[8]   Vascular extracellular matrix remodeling in cerebral aneurysms [J].
Bruno, G ;
Todor, R ;
Lewis, I ;
Chyatte, D .
JOURNAL OF NEUROSURGERY, 1998, 89 (03) :431-440
[9]   Endothelial dysfunction in cardiovascular diseases - The role of oxidant stress [J].
Cai, H ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 87 (10) :840-844
[10]  
Chen XL, 1998, CIRC RES, V83, P952