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XW630对去卵巢大鼠骨质疏松的作用(英文)
作者姓名:Sun L  Qiu MC  Weng LL  Zheng H  Liu JS
作者单位:中国协和医科大学基础医学院药理室,天津医科大学总医院内分泌科,华西医科大学药学院,华西医科大学药学院,中国医学科学院基础医学研究所 北京 10000 中国,天津 300052 中国,成都 610041 中国,成都 610041 中国
基金项目:Project supported by the National Natural Science Foundation of China, No 39430120.
摘    要:目的:研究XW630对去卵巢大鼠骨质疏松的影响。方法:血清E_2和骨钙素(BGP)浓度用放射免疫测定法。骨组织计量学用四环素内标法。结果:去卵巢后,血清E_2水平下降61.9%,子宫减轻72.7%,动情次数减少63.6%。XW630治疗13周后,血清BGP浓度增加75.7%,动情次数略增加,但低于假手术组,血清E_2浓度及子宫重量无明显变化。与OVX组相比,XW630组骨组织计量学指标TBV/TTV,TBV/SBV和MTPD增加;Sfract(s),Sfract(d),TOS和Svf增加,OMP缩短。结论:XW630增加骨激活频率、骨小梁连接性、稳定性和张力。表明XW630促进骨形成、抑制骨吸收,对生殖系统无影响。

关 键 词:XW630  四环素类  雌二醇  骨质疏松  卵巢切除术  股骨  放射免疫测定  子宫  阴道涂片

Effects of 2-[3-estrone-N-ethyl-piperazine-methyl]tetracycline (XW630) on osteoporosis in ovariectomized rats
Sun L,Qiu MC,Weng LL,Zheng H,Liu JS.Effects of 2-[3-estrone-N-ethyl-piperazine-methyl]tetracycline (XW630) on osteoporosis in ovariectomized rats[J].Acta Pharmacologica Sinica,2000,21(3):200-204.
Authors:Sun L  Qiu M C  Weng L L  Zheng H  Liu J S
Institution:Department of Pharmacology, Institute of Basic Medical Sciences, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100005, China.
Abstract:AIM: To study the effects of 2-3-estrone-N-ethyl-piperazine-methyl]tetracycline (XW630) on experimental osteoporosis in ovariectomized (OVX) rats. METHODS: Serum estradiol (E2) content and bone 1-carboxyglutamic acid-containing protein (BGP) content were measured by radioimmunoassay. With undecalcified bone section and tetracycline intraperitoneal labeling, the bone static and dynamic data were studied in right femur samples. RESULTS: After treatment with XW630 2.5 mg.kg-1, serum BGP content increased by 75.7% but there was no change in serum E2 content and uterus weight compared with OVX rats. Compared with OVX rats, the static data of trabecular bone volume/total tissue volume, trabecular bone volume/sponge bone volume, and mean trabecular plate density were enhanced after treatment with XW630 for 13 wk. The dynamic data of single-labeled surface, double-labeled surface, trabecular osteoid surface, and bone formation rate in tissue level in XW630 group were increased and osteoid maturation period was shortened. CONCLUSION: XW630 enhanced bone activation frequency and increased trabecular connectivity, stability, and strength. XW630 stimulated bone formation and inhibited bone resorption with no effect on reproductive system.
Keywords:XW630  tetracyclines  estradiol  osteoporosis  ovariectomy  femur  radioimmunoassay  uterus  vaginal smears
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