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乙烷-1-羟基-1,1-二膦酸盐(EHDP)对破骨细胞核掺入和积聚的影响。

Ethane-1-hydroxy-1, 1-diphosphonate (EHDP) effects on incorporation and accumulation of osteoclast nuclei.

作者信息

Miller S C, Jee W S, Kimmel D B, Woodbury L

出版信息

Calcif Tissue Res. 1977 Feb 11;22(3):243-52. doi: 10.1007/BF02010363.

Abstract

Male rats weighing 100 g were injected with vehicle (control group), 0.4 or 4.0 mg/kg/day of ethane-1-hydroxy-1,1-diphosphonate (EHDP). Beginning after 6 days of EHDP treatment all rats received six subcutaneous injections of 3H-thymidine at 8 h intervals. The multiple labeling index of autoradiographically defined labeled cells was determined for the osteoprogenitor cells of the primary spongiosa of the proximal tibial metaphysis. The osteoclasts in the proximal tibial metaphisis were assayed for population parameters and incorporation of labeled nuclei at sequential intervals after the administration of 3H-thymidine. After 6 days of EHDP pre-treatment the multiple labeling index of the osteoprogenitor cells was reduced with 4.0 mg/kg/day dose of EHDP. At the beginning of the experimental kinetic sampling period, after the 6 days of EHDP pre-treatment, EHDP treatment resulted in significant increases in the numbers of osteoclasts, nuclei per osteoclast profile, and total osteoclast nuclei. During the sampling period, the 4.0 mg/kg/day dose of EHDP caused further increases in the number of total osteoclasts. EHDP treatment caused a marked increase in the rate of incorporation and accumulation of 3H-thymidine-labeled nuclei in osteoclasts. Thus, EHDP causes an accelerated rate of osteoclast production from percursor cells in spite of its ability to slow bone resorption. Although the origin of osteoclast nuclei is not clear, the kinetic data from this study suggests that osteoclast nuclei are not arising from osteoprogenitor cells or osteocytes in the EHDP-treated animals.

摘要

给体重100克的雄性大鼠注射赋形剂(对照组)、0.4或4.0毫克/千克/天的乙烷-1-羟基-1,1-二膦酸盐(EHDP)。在EHDP治疗6天后,所有大鼠每隔8小时接受6次皮下注射3H-胸腺嘧啶核苷。对胫骨近端干骺端初级海绵骨的骨祖细胞,测定放射自显影定义的标记细胞的多重标记指数。在给予3H-胸腺嘧啶核苷后,对胫骨近端干骺端的破骨细胞进行群体参数测定和连续时间间隔的标记核掺入情况分析。EHDP预处理6天后,4.0毫克/千克/天剂量的EHDP使骨祖细胞的多重标记指数降低。在EHDP预处理6天后的实验动力学采样期开始时,EHDP治疗导致破骨细胞数量、每个破骨细胞轮廓中的核数量以及破骨细胞核总数显著增加。在采样期内,4.0毫克/千克/天剂量的EHDP使破骨细胞总数进一步增加。EHDP治疗使破骨细胞中3H-胸腺嘧啶核苷标记核的掺入和积累速率显著增加。因此,尽管EHDP有减缓骨吸收的能力,但它会导致前体细胞产生破骨细胞的速率加快。虽然破骨细胞核的来源尚不清楚,但本研究的动力学数据表明,在接受EHDP治疗的动物中,破骨细胞核并非来自骨祖细胞或骨细胞。

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