The role of estrogen in the formation of experimental abdominal aortic aneurysm

被引:59
作者
Wu, Xiao-Fei [1 ]
Zhang, Jian [2 ]
Paskauskas, Saulius [3 ]
Xin, Shi-Jie [2 ]
Duan, Zhi-Quan [2 ]
机构
[1] DaLian Univ, Affilialed ZhongShan Hosp, Gen Surg Dept 3, Dalian 116001, Peoples R China
[2] China Med Univ, Affiliated Hosp 1, Gen Surg Dept 3, Shenyang, Peoples R China
[3] Kaunas Univ Med, Dept Gen Surg, LT-500009 Kaunas, Lithuania
关键词
Aortic aneurysm; Abdominal; Estrogen; Matrix metalloproteinase; HORMONE REPLACEMENT THERAPY; FACTOR-KAPPA-B; MATRIX METALLOPROTEINASES; IN-VIVO; ATHEROSCLEROSIS; EXPRESSION; ADHESION; RECEPTOR; TRANSCRIPTION; PREVALENCE;
D O I
10.1016/j.amjsurg.2007.11.022
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
OBJECTIVE: The current study sought to investigate the role of estrogen in the formation of experimental abdominal aortic aneurysm (AAA). METHODS: Elastase perfusion of infrarenal AAA animal model was performed in 20 female and 20 male Wistar rats that were randomly divided into,in ovariectomized/sham-operated group and an estradiol (E2) experimental/saline control group, respectively. At day 14, E2 was detected, while the mRNA and protein expressions of matrix metalloproteinases 2 and 9 (MMP-2 and -9) in AAA tissue were detected by immunohistochemistry and polymerase chain reaction (PCR). RESULTS: The ovariectomized group showed lower estrogen levels and a higher aneurysm dilatation rate and significantly higher MMP-2 and -9 expression compared with the sham-operated group (P<.01), which was in accordance with MMP-2 and -9 mRNA expression. The E2 group showed higher estrogen levels and a lower aneurysm dilatation rate and significantly lower MMP-2 and -9 expression than did the saline control group (P<.01), which was in accordance with MMP-2 and -9 mRNA expression. CONCLUSIONS: In the pathogenesis of AAA, estrogen may play an inhibitory role by decreasing expression of MMP-2 and MMP-9 synthesis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 54
页数:6
相关论文
共 28 条
[1]
ELASTASE-INDUCED EXPERIMENTAL ANEURYSMS IN RATS [J].
ANIDJAR, S ;
SALZMANN, JL ;
GENTRIC, D ;
LAGNEAU, P ;
CAMILLERI, JP ;
MICHEL, JB .
CIRCULATION, 1990, 82 (03) :973-981
[2]
Incidence and prevalence of abdominal aortic aneurysms, estimated by necropsy studies and population screening by ultrasound [J].
Bengtsson, H ;
Sonesson, B ;
Bergqvist, D .
ABDOMINAL AORTIC ANEURYSM: GENETICS, PATHOPHYSIOLOGY, AND MOLECULAR BIOLOGY, 1996, 800 :1-24
[3]
Raloxifene and estrogen reduces progression of advanced atherosclerosis - a study in ovariectomized, cholesterol-fed rabbits [J].
Bjarnason, NH ;
Haarbo, J ;
Byrjalsen, I ;
Alexandersen, P ;
Kauffman, RF ;
Christiansen, C .
ATHEROSCLEROSIS, 2001, 154 (01) :97-102
[4]
Estrogen reduces atherosclerotic lesion development in apolipoprotein E-deficient mice [J].
Bourassa, PAK ;
Milos, PM ;
Gaynor, BJ ;
Breslow, JL ;
Aiello, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10022-10027
[5]
DUAN ZG, 1999, PRACTICAL VASCULAR S, P262
[6]
Reciprocal antagonism between estrogen receptor and NF-κB activity in vivo [J].
Evans, MJ ;
Eckert, A ;
Lai, K ;
Adelman, SJ ;
Harnish, DC .
CIRCULATION RESEARCH, 2001, 89 (09) :823-830
[7]
INFLAMMATION AND MATRIX METALLOPROTEINASES IN THE ENLARGING ABDOMINAL AORTIC-ANEURYSM [J].
FREESTONE, T ;
TURNER, RJ ;
COADY, A ;
HIGMAN, DJ ;
GREENHALGH, RM ;
POWELL, JT .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (08) :1145-1151
[8]
The role of CBP in estrogen receptor cross-talk with nuclear factor-κB in HepG2 cells [J].
Harnish, DC ;
Scicchitano, MS ;
Adelman, SJ ;
Lyttle, CR ;
Karathanasis, SK .
ENDOCRINOLOGY, 2000, 141 (09) :3403-3411
[9]
MENSTRUAL AND REPRODUCTIVE FACTORS AND THE RISK OF MYOCARDIAL-INFARCTION IN WOMEN UNDER 55 YEARS OF AGE [J].
LAVECCHIA, C ;
DECARLI, A ;
FRANCESCHI, S ;
GENTILE, A ;
NEGRI, E ;
PARAZZINI, F .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (05) :1108-1112
[10]
LIU YC, 1999, FOREIGN MED SCI OBST, V26, P266