The effect of percutaneous oestradiol on atheroma formation in ovariectomized cholesterol-fed rabbits

被引:8
作者
Haines, CJ [1 ]
James, AE
Panesar, NS
Ngai, TJ
Sahota, DS
Jones, RL
Chang, AMZ
机构
[1] Chinese Univ Hong Kong, Dept Obstet & Gynaecol, Shatin, New Territories, Hong Kong
[2] Prince Wales Hosp, Shatin, New Territories, Hong Kong
[3] Chinese Univ Hong Kong, Lab Anim Serv Ctr, Shatin, New Territories, Hong Kong
[4] Chinese Univ Hong Kong, Dept Chem Pathol, Shatin, New Territories, Hong Kong
[5] Chinese Univ Hong Kong, Dept Pharmacol, Shatin, New Territories, Hong Kong
关键词
atherosclerosis; cholesterol; oestrogen;
D O I
10.1016/S0021-9150(98)00327-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The aim of this study was to examine the effect of percutaneous oestradiol on the lipid profile and on atheroma formation using an animal model. Methods: The study was of 12 weeks duration. Fifty sexually mature female New Zealand White rabbits were divided into five groups of equal size. Two groups acted as controls and received normal rabbit chow. Rabbits in one of these groups were ovariectomized. The remaining three groups were ovariectomized but received 1% cholesterol enriched rabbit chow. One of these cholesterol-fed groups received 0.3 mg/kg percutaneous oestradiol daily whilst another received 0.1 mg/kg oral oestradiol daily. Measurements of concentrations of total cholesterol (TC), high density lipoprotein cholesterol (HDL-C) and triglycerides (TC) were made at the beginning and end of the study. Aortic atheroma formation was measured using computerized image analysis of uptake of Sudan III staining. Results: After 12 weeks there were significant increases in the mean concentrations of TC in the three cholesterol-fed groups compared with controls (P < 0.001). Changes in HDL-C and TG concentrations were less consistent. The mean area of aortic atheroma formation was significantly less in both the percutaneous oestradiol group (4.9%) and the oral oestradiol group (8.6%) compared with the non-oestrogen-treated cholesterol-fed group (19.5%) (P < 0.001, < 0.01 respectively). Conclusion: These results suggest that percutaneous oestradiol has a direct protective effect on atheroma formation independent of serum concentrations of total cholesterol. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 35 条
[1]   OVARIECTOMY, SOCIAL-STATUS, AND ATHEROSCLEROSIS IN CYNOMOLGUS MONKEYS [J].
ADAMS, MR ;
KAPLAN, JR ;
CLARKSON, TB ;
KORITNIK, DR .
ARTERIOSCLEROSIS, 1985, 5 (02) :192-200
[2]   INHIBITION OF CORONARY-ARTERY ATHEROSCLEROSIS BY 17-BETA ESTRADIOL IN OVARIECTOMIZED MONKEYS - LACK OF AN EFFECT OF ADDED PROGESTERONE [J].
ADAMS, MR ;
KAPLAN, JR ;
MANUCK, SB ;
KORITNIK, DR ;
PARKS, JS ;
WOLFE, MS ;
CLARKSON, TB .
ARTERIOSCLEROSIS, 1990, 10 (06) :1051-1057
[3]  
BASDEVANT A, 1991, FERTIL STERIL, V55, P1112
[4]   The menopausal transition [J].
Burger, HG .
BAILLIERES CLINICAL OBSTETRICS AND GYNAECOLOGY, 1996, 10 (03) :347-359
[5]   BONE-MINERAL DENSITY IN SURGICALLY POSTMENOPAUSAL WOMEN RECEIVING HORMONAL REPLACEMENT THERAPY AS ASSESSED BY DUAL PHOTON-ABSORPTIOMETRY [J].
CASTELOBRANCO, C ;
PONS, F ;
GONZALEZMERLO, J .
MATURITAS, 1993, 16 (02) :133-137
[6]   BIOLOGIC EFFECTS OF TRANSDERMAL ESTRADIOL [J].
CHETKOWSKI, RJ ;
MELDRUM, DR ;
STEINGOLD, KA ;
RANDLE, D ;
LU, JK ;
EGGENA, P ;
HERSHMAN, JM ;
ALKJAERSIG, NK ;
FLETCHER, AP ;
JUDD, HL .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (25) :1615-1620
[7]  
CLARKSON TB, 1994, FERTIL STERIL, V62, pS147
[8]   BIOLOGICAL EFFECTS OF ESTRADIOL-17-BETA-IN POSTMENOPAUSAL WOMEN - ORAL VERSUS PERCUTANEOUS ADMINISTRATION [J].
DELIGNIERES, B ;
BASDEVANT, A ;
THOMAS, G ;
THALABARD, JC ;
MERCIERBODARD, C ;
CONARD, J ;
GUYENE, TT ;
MAIRON, N ;
CORVOL, P ;
GUYGRAND, B ;
MAUVAISJARVIS, P ;
SITRUKWARE, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 62 (03) :536-541
[9]   COMPARATIVE ENDOCRINOLOGIC AND CLINICAL EFFECTS OF PERCUTANEOUS ESTRADIOL AND ORAL CONJUGATED ESTROGENS AS REPLACEMENT THERAPY IN MENOPAUSAL WOMEN [J].
DUPONT, A ;
DUPONT, P ;
CUSAN, L ;
TREMBLAY, M ;
RIOUX, J ;
CLOUTIER, D ;
MAILLOUX, J ;
DELIGNIERES, B ;
GUTKOWSKA, J ;
BOUCHER, H ;
BELANGER, A ;
MOYER, DL ;
MOORJANI, S ;
LABRIE, F .
MATURITAS, 1991, 13 (04) :297-311
[10]  
GANGAR KF, 1991, LANCET, V338, P839