دورية أكاديمية

Estrogen-induced osteogenesis in intact female mice lacking ERβ.

التفاصيل البيبلوغرافية
العنوان: Estrogen-induced osteogenesis in intact female mice lacking ERβ.
المؤلفون: McDougall, K.E., Perry, M.J., Gibson, R.L., Bright, J.M., Colley, S.M., Hodgin, J.B., Smithies, O., Tobias, J.H.
المصدر: American Journal of Physiology: Endocrinology & Metabolism; Oct2002, Vol. 46 Issue 4, pE817, 7p, 6 Black and White Photographs, 2 Charts, 8 Graphs
مصطلحات موضوعية: ESTROGEN receptors, BONE growth
مستخلص: We recently found that estrogen receptor (ER) antagonists prevent highdose estrogen from inducing the formation of new cancellous bone within the medullary cavity of mouse long bones. In the present investigation, we studied the role of specific ER subtypes in this response by examining whether this is impaired in female ERβ[sup -/-] mice previously generated by targeted gene deletion. Vehicle or 17β-estradiol (E[sub 2]) (range 4-4,000 µg·kg[sup -1]·day[sup -1]) was administered to intact female ERβ[sup -/-] mice and wild-type littermates by subcutaneous injection for 28 days. The osteogenic response was subsequently assessed by histomorphometry performed on longitudinal and cross sections of the tibia. E[sub 2] was found to cause an equivalent increase in cancellous bone formation in ERβ[sup -/-] mice and littermate controls, as assessed at the proximal and distal regions of the proximal tibial metaphysis. E[sub 2] also resulted in a similar increase in endosteal mineral apposition rate in these two genotypes, as assessed at the tibial diaphysis. In contrast, cortical area in ERβ[sup -/-] mice was found to be greater than that in wild types irrespective of E[sub 2] treatment, as was tibial bone mineral density as measured by dual-energy X-ray absorptiometry, consistent with previous reports of increased cortical bone mass in these animals. We conclude that, although ERβ acts as a negative modulator of cortical modeling, this isoform does not appear to contribute to high-dose estrogen's ability to induce new cancellous bone formation in mouse long bones. [ABSTRACT FROM AUTHOR]
Copyright of American Journal of Physiology: Endocrinology & Metabolism is the property of American Physiological Society and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:01931849
DOI:10.1152/ajpendo.00071.2002