Molinuevo María Silvina, Fernández Juan Manuel, Cortizo Ana María, McCarthy Antonio Desmond, Schurman León, Sedlinsky Claudia
Laboratorio de Investigación en Osteopatías y Metabolismo Mineral, Facultad de Ciencias Exactas, Universidad Nacional de La Plata. 47 y 115, (1900) La Plata, Argentina.
Laboratorio de Investigación en Osteopatías y Metabolismo Mineral, Facultad de Ciencias Exactas, Universidad Nacional de La Plata. 47 y 115, (1900) La Plata, Argentina.
Mol Cell Endocrinol. 2017 Jul 15;450:94-104. doi: 10.1016/j.mce.2017.04.022. Epub 2017 Apr 26.
Advanced glycation end products (AGE) have been demonstrated to induce the osteogenic trans-differentiation of vascular smooth muscle cells (VSMC). Strontium ranelate (SR) is an anti-osteoporotic agent that has both anti-catabolic and anabolic actions on bone tissue. However, in the last years SR has been associated with an increase of cardiovascular risk. We hypothesize that SR can increase the osteoblastic trans-differentiation of VSMC and the induction of extracellular calcifications, an effect that could be potentiated in the presence of AGE and inhibited by simultaneous administration of vitamin D. The present results of our in vitro experiments demonstrate that AGE and SR alone or in combination, stimulate L-type calcium channels, causing an increase in reactive oxygen species and activation of both ERK and NFkB, with the final effect of promoting the osteogenic shift of VSMC. Importantly, these in vitro effects of AGE and/or SR can be prevented by co-incubation with vitamin D.
晚期糖基化终末产物(AGE)已被证明可诱导血管平滑肌细胞(VSMC)向成骨细胞转分化。雷奈酸锶(SR)是一种抗骨质疏松药物,对骨组织具有抗分解代谢和合成代谢作用。然而,近年来SR与心血管风险增加有关。我们推测,SR可增加VSMC向成骨细胞的转分化以及细胞外钙化的诱导,在AGE存在的情况下这种作用可能会增强,而同时给予维生素D可抑制这种作用。我们体外实验的当前结果表明,单独或联合使用AGE和SR会刺激L型钙通道,导致活性氧增加以及ERK和NFkB的激活,最终促进VSMC的成骨转变。重要的是,AGE和/或SR的这些体外作用可通过与维生素D共同孵育来预防。