Suppr超能文献

间歇性视黄酸联合持续使用17β-雌二醇可增加骨质疏松性去卵巢大鼠的松质骨体积。

Intermittent retinoic acid in combination with continuous oestradiol-17 beta increases cancellous bone volume in osteopaenic ovariectomized rats.

作者信息

Tobias J H, Gallagher A, Chambers T J

机构信息

Department of Histopathology, St George's Hospital Medical School, London, UK.

出版信息

J Endocrinol. 1994 Jul;142(1):61-7. doi: 10.1677/joe.0.1420061.

Abstract

Although short-term administration of oestradiol-17 beta (OE2) stimulates cancellous bone formation in the rat, this is replaced by a tendency to suppression after prolonged treatment. Hence, in rats rendered osteopaenic by ovariectomy, OE2 administration fails either to induce a sustained increase in bone formation or to restore bone volume. A possible explanation for this failure is that OE2 also inhibits bone resorption, secondarily suppressing bone formation through coupling mechanisms. We therefore investigated whether the effects of OE2 treatment might be modified by intermittently stimulating bone resorption with retinoic acid (120mg/kg daily) for 4 out of every 20 days. We found, in a preliminary experiment using intact animals, that intermittent retinoic acid reduced cancellous bone volume, consistent with previously documented stimulation of bone resorption by retinoic acid. Rats were then rendered osteopaenic by ovariectomy, and given vehicle, retinoic acid and/or OE2. We found that animals treated with intermittent retinoic acid and OE2 showed a substantial increase in cancellous bone volume compared with ovariectomized animals treated with vehicle, retinoic acid alone or OE2 alone. Therefore, intermittent retinoic acid appears to cause a net increase in bone formation over resorption when given to ovariectomized animals in conjunction with OE2. We conclude that the effects of OE2 on cancellous bone are modified by intermittent treatment with retinoic acid, resulting in a substantial increase in bone volume.

摘要

虽然短期给予17β-雌二醇(OE2)可刺激大鼠松质骨形成,但长期治疗后这种刺激作用会被抑制趋势所取代。因此,在因卵巢切除而导致骨质疏松的大鼠中,给予OE2既不能诱导骨形成持续增加,也不能恢复骨量。这种失败的一个可能解释是,OE2还抑制骨吸收,进而通过耦合机制抑制骨形成。因此,我们研究了是否可以通过每20天中的4天用视黄酸(每日120mg/kg)间歇刺激骨吸收来改变OE2治疗的效果。在一项使用未切除卵巢动物的初步实验中,我们发现间歇性给予视黄酸会减少松质骨体积,这与之前记录的视黄酸刺激骨吸收的结果一致。然后通过卵巢切除使大鼠骨质疏松,并给予赋形剂、视黄酸和/或OE2。我们发现,与接受赋形剂、单独视黄酸或单独OE2治疗的卵巢切除动物相比,接受间歇性视黄酸和OE2治疗的动物松质骨体积显著增加。因此,在给卵巢切除动物联合使用OE2时,间歇性视黄酸似乎会导致骨形成相对于骨吸收的净增加。我们得出结论,视黄酸的间歇性治疗改变了OE2对松质骨的作用,导致骨量显著增加。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验