Oestrogen and the cardiovascular system: the good, the bad and the puzzling

被引:32
作者
Gray, GA
Sharif, I
Webb, DJ
Seckl, JR
机构
[1] Univ Edinburgh, Ctr Cardiovasc Sci, Dept Biomed Sci, Edinburgh EH8 9XD, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Cardiovasc Sci, Dept Med Sci, Edinburgh EH4 2XU, Midlothian, Scotland
[3] Univ Edinburgh, Western Gen Hosp, Mol Med Ctr, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1016/S0165-6147(00)01640-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The concept that oestrogen replacement therapy is cardioprotective has been challenged recently by the negative results of randomized clinical trials in coronary heart disease. These data have come at a time of rapid advances in our understanding of the cellular mechanisms of oestrogen. in particular,the cloning of the classical oestrogen receptor (ER alpha), the identification of a novel ER isoform (ER beta), the availability of specific ER alpha and ER beta knockout mice models, and the elucidation of receptor functions and signalling pathways linked to non-genomic actions of oestrogen are helping to unravel this complex biology. In this article, these advances will be discussed with particular emphasis on the regulation of nitric oxide synthesis by oestrogen, Furthermore, the puzzling issues that have emerged and the potential for development of novel and specific therapeutic approaches will be highlighted.
引用
收藏
页码:152 / 156
页数:5
相关论文
共 47 条
[31]   Association of estrogen receptor β (ESR2) gene polymorphism with blood pressure [J].
Ogawa, S ;
Emi, M ;
Shiraki, M ;
Hosoi, T ;
Ouchi, Y ;
Inoue, S .
JOURNAL OF HUMAN GENETICS, 2000, 45 (06) :327-330
[32]   Signaling through scaffold, anchoring, and adaptor proteins [J].
Pawson, T ;
Scott, JD .
SCIENCE, 1997, 278 (5346) :2075-2080
[33]   SPECIFIC BINDING-SITES FOR ESTROGEN AT OUTER SURFACES OF ISOLATED ENDOMETRIAL CELLS [J].
PIETRAS, RJ ;
SZEGO, CM .
NATURE, 1977, 265 (5589) :69-72
[34]   Structural aspects of agonism and antagonism in the oestrogen receptor [J].
Pike, ACW ;
Brzozowski, AM ;
Walton, J ;
Hubbard, RE ;
Bonn, T ;
Gustafsson, JÅ ;
Carlquist, M .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2000, 28 :396-400
[35]   Methylation of the estrogen receptor gene is associated with aging and atherosclerosis in the cardiovascular system [J].
Post, WS ;
Goldschmidt-Clermont, PJ ;
Wilhide, CC ;
Heldman, AW ;
Sussman, MS ;
Ouyang, P ;
Milliken, EE ;
Issa, JPJ .
CARDIOVASCULAR RESEARCH, 1999, 43 (04) :985-991
[36]   Cell membrane and nuclear estrogen receptors (ERs) originate from a single transcript:: Studies of ERα and ERβ expressed in Chinese hamster ovary cells [J].
Razandi, M ;
Pedram, A ;
Greene, GL ;
Levin, ER .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (02) :307-319
[37]   ISOLATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN ENDOTHELIAL NITRIC-OXIDE SYNTHASE (NOS3) GENE [J].
ROBINSON, LJ ;
WEREMOWICZ, S ;
MORTON, CC ;
MICHEL, T .
GENOMICS, 1994, 19 (02) :350-357
[38]   Differential effects of xenoestrogens on coactivator recruitment by estrogen receptor (ER) α and ERβ [J].
Routledge, EJ ;
White, R ;
Parker, MG ;
Sumpter, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (46) :35986-35993
[39]   Human vascular endothelial cells contain membrane binding sites for estradiol, which mediate rapid intracellular signaling [J].
Russell, KS ;
Haynes, MP ;
Sinha, D ;
Clerisme, E ;
Bender, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5930-5935
[40]   Rapid activation of endothelial nitric oxide synthase by estrogen [J].
Shaul, PW .
STEROIDS, 1999, 64 (1-2) :28-34