Estrogen inhibits the vascular injury response in estrogen receptor β-deficient female mice

被引:220
|
作者
Karas, RH
Hodgin, JB
Kwoun, M
Krege, JH
Aronovitz, M
Mackey, W
Gustafsson, JÅ
Korach, KS
Smithies, O
Mendelsohn, ME
机构
[1] New England Med Ctr Hosp Inc, Mol Cardiol Res Inst, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
[3] Tufts Univ, Sch Med, Dept Vasc Surg, Boston, MA 02111 USA
[4] Univ N Carolina, Dept Pathol & Lab Med, Chapel Hill, NC 27709 USA
[5] NIEHS, Res Triangle Pk, NC 27709 USA
[6] Karolinska Inst, Dept Med Nutr, S-14186 Huddinge, Sweden
关键词
17; beta-estradiol; vascular smooth muscle;
D O I
10.1073/pnas.96.26.15133
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The protective effects of estrogen in the cardiovascular system result from both systemic effects and direct actions of the hormone on the vasculature. Two estrogen receptors have been identified, ER alpha and ER beta. We demonstrated previously that estrogen inhibits the response to vascular injury in both wild-type and ER alpha-deficient mice, and that ER beta is expressed in the blood vessels of each, suggesting a role for ER beta in the vascular protective effects of estrogen. In the present study, we examined the effect of estrogen administration on mouse carotid arterial injury in ER beta-deficient mice. Surprisingly, in ovariectomized female wild-type and ER beta knockout mice, 17 beta-estradiol markedly and equally inhibited the increase in vascular medial area and the proliferation of vascular smooth muscle cells after vascular injury, These data demonstrate that ER beta is not required for estrogen-mediated inhibition of the response to vascular injury, and suggest that either of the two known estrogen receptors is sufficient to protect against vascular injury, or that another unidentified estrogen receptor mediates the vascular protective effects of estrogen.
引用
收藏
页码:15133 / 15136
页数:4
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