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Melatonin promotes osteoblast differentiation of bone marrow mesenchymal stem cells in aged rats

机译:褪黑素促进老年大鼠骨髓间充质干细胞的成骨细胞分化

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OBJECTIVE: The current study was to explore the effect of melatonin on osteoporosis and relevant mechanisms. MATERIALS AND METHODS: We performed micro-CT to detect bone microstructure and ELISA to detect the contents of osteocalcin (OCN) and bone alkaline phosphatase (BAP) in serum. Double fluorescence labeling of calcein and tetracycline and toluidine blue staining were used to determine morphological indexes of bone tissues. Alizarin red staining and Oil Red O staining were performed to recognize bone cells and adipocytes. RT-PCR was performed to determine the expression of osteoblast differentiation related genes. RESULTS: In the current study, data from micro-CT indicated that melatonin significantly increased the bone mass density (BMD), bone volume/tissue volume (BV/TV), trabecular number (Tb.N) and trabecular thickness (Tb.Th), and decreased the Structure Model Index (SMI) and trabecular Separation/Spacing (Tb.Sp) in elderly rats. Melatonin reduced calcium and phosphorus losses in urine and increased BAP and OCN levels in serum in elderly rats and increased bone formation rate (BFR) and bone mineralization rate (MAR) in elderly rats. Melatonin increased the number of osteoblasts in bone marrow and reduced the number of adipocytes in elderly rats. Melatonin also promoted the expression of osteogenic differentiation genes and suppressed the expression of adipogenic differentiation genes. CONCLUSIONS: WE suggest that melatonin could alleviate osteoporosis in aged rats’ models probably by promoting osteoblast differentiation.
机译:目的:本研究旨在探讨褪黑激素对骨质疏松症的影响及其相关机制。材料与方法:我们进行了显微CT检测骨微结构,并进行了ELISA检测血清中骨钙素(OCN)和骨碱性磷酸酶(BAP)的含量。钙黄绿素和四环素的双荧光标记和甲苯胺蓝染色用于确定骨组织的形态学指标。进行茜素红染色和油红O染色以识别骨细胞和脂肪细胞。进行RT-PCR以确定成骨细胞分化相关基因的表达。结果:在当前的研究中,来自微CT的数据表明褪黑激素显着​​增加了骨密度(BMD),骨体积/组织体积(BV / TV),小梁数目(Tb.N)和小梁厚度(Tb.Th) ),并降低了老年大鼠的结构模型指数(SMI)和小梁分离/间距(Tb.Sp)。褪黑素减少了老年大鼠尿液中钙和磷的流失,并增加了血清中BAP和OCN的水平,并增加了老年大鼠的骨形成率(BFR)和骨矿化率(MAR)。褪黑素增加了老年大鼠骨髓中成骨细胞的数量,减少了脂肪细胞的数量。褪黑素还促进成骨分化基因的表达,并抑制成脂分化基因的表达。结论:我们认为褪黑激素可能通过促进成骨细胞分化来减轻老年大鼠模型的骨质疏松症。

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