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Effects of alendronate and pamidronate on cultured rat metatarsal bones: failure to prevent dexamethasone-induced growth retardation.

机译:阿仑膦酸和帕米膦酸对培养的大鼠meta骨的影响:未能阻止地塞米松诱导的生长迟缓。

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Bisphosphonates are widely used anti-resorptive drugs in the adult population. In children, their use has mainly been limited to patients with osteogenesis imperfecta. However, the powerful effects of bisphosphonates on bone turnover have raised concern about their long-term effects on the growing skeleton. We aimed to study the effects of two commonly used bisphosphonates, alendronate (Aln) and pamidronate (Pam) on normal bone growth as well as their potential to prevent glucocorticoid-induced growth retardation. Effects on bone growth were studied in fetal rat metatarsal bones (day E20) that were cultured for 5-47 days and measured every 2-7 days. Cellular mechanisms were investigated in metatarsal bones and also in the human chondrocytic cell line HCS-2/8. Chondrocyte viability (WST-1), proliferation (BrdU incorporation), differentiation (collagen type X immunohistochemistry) and apoptosis (TUNEL and Cell Death ELISA) were determined. At a clinically relevant concentration of bisphosphonates (1 microM), metatarsal bone growth was stimulated by both Aln (p<0.001 for length and p<0.05 for width) and Pam (p<0.05 for both length and width) from day 19 of culture. The growth-stimulatory effect was associated with increased chondrocyte proliferation (+21% with Aln and +24% with Pam), while cell differentiation and apoptosis were not affected. Despite the finding that both Aln and Pam (1 muM) rescued HCS-2/8 cells from undergoing dexamethasone-induced apoptosis, neither of them was able to prevent dexamethasone-induced growth retardation of fetal rat metatarsal bones. Aln and Pam have the capacity to stimulate the growth of cultured fetal rat metatarsal bones; an effect associated with increased proliferation of growth plate chondrocytes. Our experimental data suggest that bisphosphonates are ineffective in preventing glucocorticoid-induced growth retardation. Nevertheless, based on our in vitro data, both Aln and Pam appear safe to use in growing children, at least with regard to their effects on linear bone growth.
机译:双膦酸盐是成年人口中广泛使用的抗吸收药物。在儿童中,其使用主要限于成骨不全症患者。然而,双膦酸盐对骨骼更新的强大影响引起了人们对其长期对骨骼生长的影响的担忧。我们旨在研究两种常用的双膦酸盐(阿仑膦酸盐(Aln)和帕米膦酸盐(Pam))对正常骨骼生长的影响,以及它们预防糖皮质激素诱导的生长迟缓的潜力。在培养5-47天并每2-7天测量一次的胎鼠meta骨(E20天)中研究了对骨生长的影响。在meta骨和人类软骨细胞系HCS-2 / 8中研究了细胞机制。测定了软骨细胞的活力(WST-1),增殖(BrdU掺入),分化(胶原X型免疫组织化学)和凋亡(TUNEL和细胞死亡ELISA)。从临床第19天起,在具有临床相关浓度的双膦酸盐(1 microM)下,Aln(长度p <0.001,宽度p <0.05)和Pam(长度和宽度p <0.05)都刺激meta骨生长。 。生长刺激作用与软骨细胞增殖增加有关(Aln + 21%,Pam + 24%),而细胞分化和凋亡不受影响。尽管发现Aln和Pam(1μM)都能使HCS-2 / 8细胞从地塞米松诱导的细胞凋亡中解救出来,但它们都不能阻止地塞米松诱导的胎鼠meta骨生长迟缓。 Aln和Pam具有刺激培养的胎鼠meta骨生长的能力。与生长板软骨细胞增殖增加有关的作用。我们的实验数据表明,双膦酸盐在预防糖皮质激素诱导的生长迟缓方面无效。然而,根据我们的体外数据,至少在他们对线性骨生长的影响方面,Aln和Pam似乎可以安全地用于成长中的儿童。

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