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用高剂量1,25 - 二羟基维生素D3对大鼠进行短期治疗可刺激骨形成并增加骨髓中成骨细胞前体细胞的数量。

Short-term treatment of rats with high dose 1,25-dihydroxyvitamin D3 stimulates bone formation and increases the number of osteoblast precursor cells in bone marrow.

作者信息

Erben R G, Scutt A M, Miao D, Kollenkirchen U, Haberey M

机构信息

Institute of Physiology, Physiological Chemistry and Animal Nutrition, Ludwig Maximilians University, Munich, Germany.

出版信息

Endocrinology. 1997 Nov;138(11):4629-35. doi: 10.1210/endo.138.11.5511.

Abstract

Using an experimental rat model, this study was undertaken to assess the effects of a short-term application of high dose 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] on calcium homeostasis, cancellous bone formation, and numbers of osteoblast precursors in ex vivo bone marrow cultures. For Exp 1 and 2, 6-month-old female rats were sc injected with either 0.2 microg 1,25-(OH)2D3/kg x day or vehicle on days 1, 2, and 3 of the studies. Serum calcium and urinary excretion of calcium were monitored for 12 days in Exp 1. In Exp 2, the rats were ip labeled with five different fluorochromes on days 0, 5, 10, 15, and 20, respectively. Half of the rats in each group were killed on day 7, the rest of the rats were killed on day 24, and the first lumbar vertebrae were processed for histomorphometry. In Exp 3, 0.2 microg 1,25-(OH)2D3/kg BW or vehicle was sc administered to 6-month-old male rats on days 1, 2, and 3, and the number of colony-forming units with the ability to express alkaline phosphatase, to calcify, and/or to synthesize collagen were enumerated sequentially on days 4, 6, 8, 10, 12, and 14 in bone marrow cultures. Short-term 1,25-(OH)2D3 treatment resulted in increased values for serum and urinary calcium during the treatment phase in Exp 1, depressed osteoclast numbers and strongly elevated osteoblast perimeter by day 7, and stimulated mineral apposition rate and bone formation rate in the interval between days 5-15 of Exp 2. Moreover, 1,25-(OH)2D3 administration to rats significantly enhanced the number of mesenchymal precursor cells in bone marrow with the ability to differentiate into an osteoblastic phenotype in ex vivo bone marrow cultures on day 4 of Exp 3. These studies provide evidence that short-term 1,25-(OH)2D3 treatment creates new bone remodeling units and augments osteoblast recruitment and osteoblast team performance in rat cancellous bone.

摘要

本研究采用实验性大鼠模型,旨在评估短期应用高剂量1,25 - 二羟基维生素D3 [1,25-(OH)2D3]对钙稳态、松质骨形成以及离体骨髓培养中成骨细胞前体细胞数量的影响。在实验1和实验2中,6月龄雌性大鼠在研究的第1、2和3天皮下注射0.2微克1,25-(OH)2D3/千克×天或赋形剂。实验1中监测血清钙和尿钙排泄12天。在实验2中,大鼠分别在第0、5、10、15和20天腹腔注射五种不同的荧光染料进行标记。每组一半的大鼠在第7天处死,其余大鼠在第24天处死,取第一腰椎进行组织形态计量学分析。在实验3中,6月龄雄性大鼠在第1、2和3天皮下注射0.2微克1,25-(OH)2D3/千克体重或赋形剂,并在骨髓培养的第4、6、8、10、12和14天依次计数具有表达碱性磷酸酶、钙化和/或合成胶原蛋白能力的集落形成单位数量。短期1,25-(OH)2D3治疗导致实验1治疗阶段血清和尿钙值升高,实验2第7天时破骨细胞数量减少且成骨细胞周长显著增加,实验2第5 - 15天期间矿物质沉积率和骨形成率受到刺激。此外,在实验3第4天,给大鼠注射1,25-(OH)2D3显著增加了骨髓中间充质前体细胞的数量,这些细胞在离体骨髓培养中具有分化为成骨细胞表型的能力。这些研究提供了证据,表明短期1,25-(OH)2D3治疗可在大鼠松质骨中创建新的骨重塑单位,并增强成骨细胞募集及成骨细胞团队功能。

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