首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Bisphosphonate effects in rat unloaded hindlimb bone loss model: three-dimensional microcomputed tomographic, histomorphometric, and densitometric analyses.
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Bisphosphonate effects in rat unloaded hindlimb bone loss model: three-dimensional microcomputed tomographic, histomorphometric, and densitometric analyses.

机译:双膦酸酯对大鼠后肢骨丢失模型的影响:三维显微计算机断层扫描,组织形态计量学和光密度分析。

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摘要

The effects of antiresorptive drugs on bone loss remain unclear. Using three-dimensional microtomography, dual X-ray/densitometry, and histomorphometry, we evaluated tiludronate effects in the bone loss model of immobilization in tail-suspended rats after 7, 13, and 23 days. Seventy-eight 12-week-old Wistar male rats were assigned to 13 groups: 1 baseline group, and for each time point, 1 control group treated with vehicle and three tail-suspended groups treated with either tiludronate (0.5 or 5 mg/kg) or vehicle, administered s. c. every other day, during the last week before sacrifice. In primary spongiosa (ISP), immobilization-induced bone loss plateaued after day 7 and was prevented by tiludronate. In secondary spongiosa (IISP), bone loss appeared at day 13 with a decrease in trabecular thickness and trabecular number (Tb.N) as assessed by three-dimensional microtomography. Osteoclastic parameters did not differ in tail-suspended rats versus control rats, whereas bone formation showed a biphasic pattern: after a marked decrease at day 7, osteoblastic activity and recruitment normalized at days 13 and 23, respectively. At day 23, the 80% decrease in bone mass was fully prevented by high-dose tiludronate with an increase in Tb.N without preventing trabecular thinning. In summary, at day 7, tiludronate prevented bone loss in ISP. After day 13, tiludronate prevented bone loss in ISP and IISP despite a further decrease in bone formation. Thus, the preventive effects of tiludronate in this model may be related to the alteration in bone modeling with an increase in Tb.N in ISP and subsequently in IISP.
机译:抗骨吸收药对骨质流失的影响尚不清楚。使用三维显微断层扫描,双重X射线/光密度法和组织形态学方法,我们评估了7天,13天和23天后固定在尾部悬吊大鼠的骨丢失模型中的替洛龙酸盐的作用。将78只12周大的Wistar雄性大鼠分为13组:1个基线组,在每个时间点,对照组分别用媒介物治疗和3个尾巴悬吊组,分别使用替洛膦酸(0.5或5 mg / kg) )或车辆,管理的。 C。每隔一天,在牺牲前的最后一周。在原发性海绵体炎(ISP)中,固定引起的骨质流失在第7天后达到稳定状态,并由替杜龙酸盐预防。在继发性海绵体炎(IISP)中,通过三维显微断层扫描评估,骨丢失在第13天出现,小梁厚度和小梁数目(Tb.N)降低。尾部悬吊的大鼠和对照组的大鼠的破骨细胞参数没有差异,而骨形成显示为双相模式:在第7天明显下降后,成骨细胞活性和募集分别在第13天和第23天恢复正常。在第23天,高剂量的tiludronate可以完全防止80%的骨量减少,而Tb.N则增加,而不会阻止小梁变薄。总之,在第7天,替洛膦酸盐预防了ISP中的骨质流失。在第13天后,尽管骨骼形成进一步减少,替洛龙酸盐仍可防止ISP和IISP中的骨骼丢失。因此,在该模型中,替洛膦酸盐的预防作用可能与骨骼模型的改变有关,随着ISP中Tb.N的增加,随后IISP中的增加。

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