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Heparin fails to potentiate the effects of IL-1β-mediated bone resorption of fetal rat long bones in vitro

机译:肝素不能在体外增强IL-1β介导的胎鼠长骨骨吸收的作用

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Heparin has been identified as a potent modulator of bone resorption. Heparin induces osteoporosis during long-term administration and has been shown in vitro to enhance the effects of other bone resorbing factors, including parathyroid hormone. In this study, we examined the effects of heparin on the bone-resorbing activity of the inflammatory cytokine IL-1β. Resorption was determined by measuring release of previously incorporated ~(45)Ca from fetal rat long bones cultured in medium supplemented with either 0.1% bovine serum albumin or 10% heat-inactivated fetal calf serum. Heparin, in the absence of serum, decreased basal resorption at 4 and 10 units/ml, and slightly increased resorption at 30 units/ml. Heparin had no effect on IL-1β-stimulated resorption. In the presence of serum, heparin induced a two-fold increase in resorption alone, however, when cocultured with IL-1β, heparin failed to further enhance IL-1β-stimulated resorption.
机译:肝素已被确定为骨吸收的有效调节剂。肝素在长期给药期间可诱发骨质疏松症,并已在体外显示出可增强其他骨吸收因子(包括甲状旁腺激素)的作用。在这项研究中,我们检查了肝素对炎性细胞因子IL-1β的骨吸收活性的影响。通过测量在掺有0.1%牛血清白蛋白或10%热灭活的胎牛血清的培养基中培养的胎鼠长骨中先前掺入的〜(45)Ca的释放来确定吸收。在无血清的情况下,肝素以4和10单位/毫升降低基础吸收,以30单位/毫升稍微增加吸收。肝素对IL-1β刺激的吸收没有影响。在存在血清的情况下,肝素单独引起的吸收增加了两倍,但是,当与IL-1β共培养时,肝素无法进一步增强IL-1β刺激的吸收。

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