Dexamethasone Use During Pregnancy: Potential Adverse Effects on Embryonic Skeletogenesis

Wnt信号通路 内分泌学 地塞米松 内科学 间充质干细胞 糖皮质激素 祖细胞 软骨发生 不利影响 胚胎干细胞 生物 医学 信号转导 干细胞 细胞生物学 遗传学 基因
作者
Xin Cheng,Guang Wang,KK Lee,Xuesong Yang
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:20 (34): 5430-5437 被引量:26
标识
DOI:10.2174/1381612820666140205144534
摘要

Glucocorticoids are important regulators of cell differentiation and mesenchymal cell lineage commitment during skeletogenesis. In clinical practice, it has been difficult to study the effects of glucocorticoids on target tissues because patients taking glucocorticoids often suffer from adverse skeletal effects. Dexamethasone (Dex) is a long-acting synthetic corticosteroid hormone that ranks amongst the most widely used prescribed drugs, and it is a powerful medication that is increasingly employed during the perinatal and neonatal periods. However, Dex is a potential teratogen. In particular, it has been claimed that Dex exposure during pregnancy can affect osteogenesis in the developing embryo, although this claim remains highly controversial. In this review, we summarize the published data from numerous clinical follow-up, animal-based and in vitro studies on the effects of Dex exposure on embryonic skeletogenesis. These studies indicate that Dex may adversely affect skeletal progenitor cells during development. In addition, Dex can exert a number of effects on bone growth at different developmental stages. We also discuss how glucocorticoids influence the BMP, FGF, Hedgehog and Wnt signaling pathways, which are key regulators of skeletogenesis in the embryo. A fuller understanding of the negative, and perhaps teratogenic, effects of Dex on skeletogenesis will have important implications for the routine use of Dex in clinical practice.
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