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抗糖尿病药物二甲双胍对培养的成骨细胞的成骨作用。

Osteogenic actions of the anti-diabetic drug metformin on osteoblasts in culture.

作者信息

Cortizo Ana M, Sedlinsky Claudia, McCarthy Antonio D, Blanco Alcira, Schurman León

机构信息

Cátedra de Bioquímica Patológica, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 1900 La Plata, and Centro de Endocrinología y Metabolismo, Hospital Francés, Buenos Aires, Argentina.

出版信息

Eur J Pharmacol. 2006 Apr 24;536(1-2):38-46. doi: 10.1016/j.ejphar.2006.02.030. Epub 2006 Feb 28.

Abstract

An association has been previously established between uncompensated diabetes mellitus and the loss of bone mineral density and/or quality. In this study, we evaluated the effects of metformin on the growth and differentiation of osteoblasts in culture. Treatment of two osteoblast-like cells (UMR106 and MC3T3E1) with metformin (25-500 microM) for 24 h led to a dose-dependent increase of cell proliferation. Metformin also promoted osteoblastic differentiation: it increased type-I collagen production in both cell lines and stimulated alkaline phosphatase activity in MC3T3E1 osteoblasts. In addition, metformin markedly increased the formation of nodules of mineralization in 3-week MC3T3E1 cultures. Metformin induced activation and redistribution of phosphorylated extracellular signal-regulated kinase (P-ERK) in a transient manner, and dose-dependently stimulated the expression of endothelial and inducible nitric oxide synthases (e/iNOS). These results show for the first time a direct osteogenic effect of metformin on osteoblasts in culture, which could be mediated by activation/redistribution of ERK-1/2 and induction of e/iNOS.

摘要

此前已证实未代偿性糖尿病与骨矿物质密度和/或质量的丧失之间存在关联。在本研究中,我们评估了二甲双胍对培养的成骨细胞生长和分化的影响。用二甲双胍(25 - 500微摩尔)处理两种成骨样细胞(UMR106和MC3T3E1)24小时导致细胞增殖呈剂量依赖性增加。二甲双胍还促进成骨细胞分化:它增加了两种细胞系中I型胶原蛋白的产生,并刺激了MC3T3E1成骨细胞中的碱性磷酸酶活性。此外,二甲双胍显著增加了3周龄MC3T3E1培养物中矿化结节的形成。二甲双胍以瞬时方式诱导磷酸化细胞外信号调节激酶(P-ERK)的激活和重新分布,并剂量依赖性地刺激内皮型和诱导型一氧化氮合酶(e/iNOS)的表达。这些结果首次表明二甲双胍对培养的成骨细胞具有直接的成骨作用,这可能是由ERK-1/2的激活/重新分布和e/iNOS的诱导介导的。

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