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雌激素通过直接诱导骨吸收破骨细胞凋亡来抑制骨吸收。

Estrogen inhibits bone resorption by directly inducing apoptosis of the bone-resorbing osteoclasts.

作者信息

Kameda T, Mano H, Yuasa T, Mori Y, Miyazawa K, Shiokawa M, Nakamaru Y, Hiroi E, Hiura K, Kameda A, Yang N N, Hakeda Y, Kumegawa M

机构信息

Department of Orthodontics, Nippon Dental University School of Dentistry at Niigata, Niigata 951, Japan.

出版信息

J Exp Med. 1997 Aug 18;186(4):489-95. doi: 10.1084/jem.186.4.489.

Abstract

Estrogen deficiency causes bone loss, which can be prevented by estrogen replacement therapy. Using a recently developed technique for isolation of highly purified mammalian osteoclasts, we showed that 17 beta-estradiol (E2) was able to directly inhibit osteoclastic bone resorption. At concentrations effective for inhibiting bone resorption, E2 also directly induced osteoclast apoptosis in a dose- and time-dependent manner. ICI164,384 and tamoxifen, as pure and partial antagonists, respectively, completely or partially blocked the effect of E2 on both inhibition of osteoclastic bone resorption and induction of osteoclast apoptosis. These data suggest that the protective effects of estrogen against postmenopausal osteoporosis are mediated in part by the direct induction of apoptosis of the bone-resorbing osteoclasts by an estrogen receptor- mediated mechanism.

摘要

雌激素缺乏会导致骨质流失,而雌激素替代疗法可以预防这种情况。利用最近开发的一种分离高度纯化的哺乳动物破骨细胞的技术,我们发现17β-雌二醇(E2)能够直接抑制破骨细胞介导的骨吸收。在有效抑制骨吸收的浓度下,E2还以剂量和时间依赖性方式直接诱导破骨细胞凋亡。ICI164,384和他莫昔芬分别作为纯拮抗剂和部分拮抗剂,完全或部分阻断了E2对抑制破骨细胞介导的骨吸收和诱导破骨细胞凋亡的作用。这些数据表明,雌激素对绝经后骨质疏松症的保护作用部分是通过雌激素受体介导的机制直接诱导骨吸收破骨细胞凋亡来实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be03/2199029/67ebad1a0691/JEM.961573f1.jpg

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