Department of Cell Biology and Genetics, Faculty of Science, Palacky University, Slechtitelu 11, 783 71 Olomouc, Czech Republic.
Toxicol Lett. 2011 Feb 5;200(3):146-53. doi: 10.1016/j.toxlet.2010.11.008. Epub 2010 Nov 27.
Valproic acid (VPA) is a wide spread anticonvulsant and mood-stabilizing agent, the use of which is associated with hepatotoxicity, bone marrow suppression and osteomalacia. In the current paper we propose a possible mechanism of VPA-induced osteomalacia involving accelerated catabolism of 1α,25(OH)(2)-vitamin D3 (VD3) due to increased expression of CYP24. We demonstrate that VPA strongly potentiates CYP24 mRNA expression by VD3 in human hepatocytes (HH) and in human embryonic kidney cells (HEK293). By the method of gene reporter assay we found that VPA increases basal and VD3-inducible activity of CYP24 promoter (pCYP24-luc) in human liver adenocarcinoma (HepG2) and in HEK293 cells in dose-dependent manner. In order to delineate the role of inhibitory effects of VPA on histone deacetylase 1 (HDAC1), we compared the effects of VPA with trichostatin A (TSA) on basal and inducible levels of CYP24 mRNA and pCYP24-luc transactivation. Transactivation of CYP24 promoter by VD3 was enhanced in the presence of both TSA and VPA. In contrast, VD3-inducible expression of CYP24 mRNA was enhanced by VPA but not by TSA, implying that HDAC1 inhibition is not the major reason for VPA effects on CYP24. We examined the effects of VPA on mitogen-activated protein kinases as the important transcriptional regulators of VDR. VPA activated extracellular signal-regulated kinase (ERK) but not c-Jun-N-terminal kinase (JNK) and p38 MAPKs. In conclusion, VPA enhances transcriptional activity of VDR and increases expression of CYP24 mRNA in the presence of VD3 in physiological concentrations. The mechanism involves activation of ERK and partly the inhibition of HDAC1.
丙戊酸(VPA)是一种广泛使用的抗惊厥和情绪稳定剂,但其使用与肝毒性、骨髓抑制和佝偻病有关。在目前的论文中,我们提出了 VPA 诱导佝偻病的可能机制,涉及由于 CYP24 表达增加导致 1α,25(OH)(2)-维生素 D3(VD3)的分解代谢加速。我们证明 VPA 可强烈增强人肝细胞(HH)和人胚肾细胞(HEK293)中 VD3 诱导的 CYP24 mRNA 表达。通过基因报告基因测定法,我们发现 VPA 以剂量依赖性方式增加人肝癌(HepG2)和 HEK293 细胞中 CYP24 启动子(pCYP24-luc)的基础和 VD3 诱导活性。为了阐明 VPA 对组蛋白去乙酰化酶 1(HDAC1)的抑制作用的作用,我们比较了 VPA 和曲古抑菌素 A(TSA)对 CYP24 mRNA 和 pCYP24-luc 反式激活的基础和诱导水平的影响。在 TSA 和 VPA 存在的情况下,VDR 的 CYP24 启动子的反式激活增强。相比之下,VPA 增强了 VD3 诱导的 CYP24 mRNA 的表达,但 TSA 没有,这表明 HDAC1 抑制不是 VPA 对 CYP24 作用的主要原因。我们检查了 VPA 对丝裂原激活的蛋白激酶(MAPK)的影响,MAPK 是 VDR 的重要转录调节剂。VPA 激活细胞外信号调节激酶(ERK),但不激活 c-Jun-N-末端激酶(JNK)和 p38 MAPK。总之,VPA 在生理浓度的 VD3 存在下增强 VDR 的转录活性并增加 CYP24 mRNA 的表达。该机制涉及 ERK 的激活和部分 HDAC1 的抑制。