| Literature DB >> 12176656 |
M K Lindberg1, Z Weihua, N Andersson, S Movérare, H Gao, O Vidal, M Erlandsson, S Windahl, G Andersson, D B Lubahn, H Carlsten, K Dahlman-Wright, J-A Gustafsson, C Ohlsson.
Abstract
Estrogen exerts a variety of important physiological effects, which have been suggested to be mediated via the two known estrogen receptors (ERs), alpha and beta. Three-month-old ovariectomized mice, lacking one or both of the two estrogen receptors, were given estrogen subcutaneously (2.3 micro g/mouse per day) and the effects on different estrogen-responsive parameters, including skeletal effects, were studied. We found that estrogen increased the cortical bone dimensions in both wild-type (WT) and double ER knockout (DERKO) mice. DNA microarray analysis was performed to characterize this effect on cortical bone and it identified four genes that were regulated by estrogen in both WT and DERKO mice. The effect of estrogen on cortical bone in DERKO mice might either be due to remaining ERalpha activity or represent an ERalpha/ERbeta-independent effect. Other effects of estrogen, such as increased trabecular bone mineral density, thymic atrophy, fat reduction and increased uterine weight, were mainly ERalpha mediated.Entities:
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Year: 2002 PMID: 12176656 DOI: 10.1677/joe.0.1740167
Source DB: PubMed Journal: J Endocrinol ISSN: 0022-0795 Impact factor: 4.286