School of Traditional Chinese Medicine, Chang Gung University, Kwei-Shan, Tao-Yuan, Taiwan, China.
Acta Pharmacol Sin. 2010 May;31(5):546-53. doi: 10.1038/aps.2010.34. Epub 2010 Apr 26.
To investigate the effects of glycyrrhetinic acid (GA), an active component extracted from the root of Glycyrrhizae glabra, on the expression of intercellular adhesion molecule-1 (ICAM-1) in tumor necrosis factor-alpha (TNF-alpha)-activated human umbilical vein endothelial cells (HUVEC).
ICAM-1 mRNA and protein levels were detected using RT-PCR and cell enzyme-linked immunosorbent assays. The adherence of human monocytic THP-1 cells labeled with [(3)H]thymidine to HUVEC was determined by counting radioactivity with a scintillation counter. The activation of mitogen-activated protein kinases as well as the degradation of I kappaB and nuclear factor-kappaB (NF-kappaB) or phospho-c-Jun in the nucleus were detected by western blots. NF-kappaB binding activity was detected using electrophoretic mobility shift assay.
GA (50 and 100 micromol/L) significantly inhibits TNF-alpha-induced ICAM-1 mRNA and protein expressions, as well as THP-1 cell adhesiveness in HUVEC. GA selectively inhibited TNF-alpha-activated signal pathway of c-Jun N-terminal kinase (JNK), without affecting extracellular signal-regulated kinase 1/2 and p38. Furthermore, GA apparently inhibited I kappaB/NF-kappaB signaling system by preventing I kappaB degradation, NF-kappaB translocation, and NF-kappaB/DNA binding activity. Finally, pretreatment with GA or the inhibitors of NF-kappaB, JNK, and p38 reduced the ICAM-1 protein expression induced by TNF-alpha.
GA inhibits TNF-alpha-stimulated ICAM-1 expression, leading to a decrease in adherent monocytes to HUVEC. This inhibition is attributed to GA interruption of both JNK/c-Jun and I kappaB/NF-kappaB signaling pathways, which decrease activator protein-1 (AP-1) and NF-kappaB mediated ICAM-1 expressions. The results suggest that GA may provide a beneficial effect in treating vascular diseases associated with inflammation, such as atherosclerosis.
研究甘草酸(GA),一种从甘草根中提取的活性成分,对肿瘤坏死因子-α(TNF-α)激活的人脐静脉内皮细胞(HUVEC)中细胞间黏附分子-1(ICAM-1)表达的影响。
采用 RT-PCR 和细胞酶联免疫吸附试验检测 ICAM-1 mRNA 和蛋白水平。用放射性计数法检测经[(3)H]胸腺嘧啶核苷标记的人单核细胞 THP-1 细胞与 HUVEC 的黏附。用 Western blot 检测丝裂原活化蛋白激酶的激活以及 IκB 和核因子-κB(NF-κB)或核磷酸化-c-Jun 的降解。用电泳迁移率变动分析检测 NF-κB 结合活性。
GA(50 和 100 μmol/L)显著抑制 TNF-α诱导的 HUVEC 中 ICAM-1 mRNA 和蛋白表达以及 THP-1 细胞黏附。GA 选择性抑制 TNF-α激活的 c-Jun N-末端激酶(JNK)信号通路,而不影响细胞外信号调节激酶 1/2 和 p38。此外,GA 通过防止 IκB 降解、NF-κB 易位以及 NF-κB/DNA 结合活性,明显抑制 IκB/NF-κB 信号系统。最后,GA 预处理或 NF-κB、JNK 和 p38 的抑制剂降低了 TNF-α诱导的 ICAM-1 蛋白表达。
GA 抑制 TNF-α刺激的 ICAM-1 表达,导致黏附于 HUVEC 的单核细胞减少。这种抑制归因于 GA 中断 JNK/c-Jun 和 IκB/NF-κB 信号通路,从而减少激活蛋白-1(AP-1)和 NF-κB 介导的 ICAM-1 表达。结果表明,GA 可能在治疗与炎症相关的血管疾病,如动脉粥样硬化方面具有有益作用。