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Ursolic Acid Inhibits Na+/K+-ATPase Activity and Prevents TNF-α-Induced Gene Expression by Blocking Amino Acid Transport and Cellular Protein Synthesis

机译:熊果酸通过阻断氨基酸转运和细胞蛋白质合成抑制Na + / K + -ATPase活性并阻止TNF-α诱导的基因表达。

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摘要

Pro-inflammatory cytokines, such as tumor necrosis factor (TNF)-α, induce the expression of a wide variety of genes, including intercellular adhesion molecule-1 (ICAM-1). Ursolic acid (3β-hydroxy-urs-12-en-28-oic acid) was identified to inhibit the cell-surface ICAM-1 expression induced by pro-inflammatory cytokines in human lung carcinoma A549 cells. Ursolic acid was found to inhibit the TNF-α-induced ICAM-1 protein expression almost completely, whereas the TNF-α-induced ICAM-1 mRNA expression and NF-κB signaling pathway were decreased only partially by ursolic acid. In line with these findings, ursolic acid prevented cellular protein synthesis as well as amino acid uptake, but did not obviously affect nucleoside uptake and the subsequent DNA/RNA syntheses. This inhibitory profile of ursolic acid was similar to that of the Na+/K+-ATPase inhibitor, ouabain, but not the translation inhibitor, cycloheximide. Consistent with this notion, ursolic acid was found to inhibit the catalytic activity of Na+/K+-ATPase. Thus, our present study reveals a novel molecular mechanism in which ursolic acid inhibits Na+/K+-ATPase activity and prevents the TNF-α-induced gene expression by blocking amino acid transport and cellular protein synthesis.
机译:促炎性细胞因子,例如肿瘤坏死因子(TNF)-α,可诱导多种基因的表达,包括细胞间粘附分子1(ICAM-1)。熊果酸(3β-羟基-urs-12-en-28-oic酸)被鉴定为抑制促炎性细胞因子在人肺癌A549细胞中诱导的细胞表面ICAM-1表达。发现熊果酸几乎完全抑制TNF-α诱导的ICAM-1蛋白表达,而熊果酸仅部分降低TNF-α诱导的ICAM-1 mRNA表达和NF-κB信号传导途径。与这些发现一致,熊果酸阻止了细胞蛋白质的合成以及氨基酸的摄取,但是并没有明显影响核苷的摄取和随后的DNA / RNA合成。熊果酸的这种抑制作用类似于Na + / K + -ATPase抑制剂哇巴因,但不包括翻译抑制剂环己酰亚胺。与该观点一致,发现熊果酸抑制Na + / K + -ATPase的催化活性。因此,我们的研究揭示了熊果酸抑制Na + / K + -ATPase活性并阻止TNF-α诱导的基因表达的新分子机制。酸转运和细胞蛋白质合成。

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