Effect of natsudaidain isolated from Citrus plants on TNF-alpha and cyclooxygenase-2 expression in RBL-2H3 cells.

T. Matsui, C. Ito, M. Itoigawa, T. Okada, H. Furukawa
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引用次数: 6

Abstract

OBJECTIVES Flavonoids inhibit the activity of chemical mediators released from mast cells. Our aim was to investigate the effects of natsudaidain, a polymethoxyflavone isolated from Citrus plants, on mast cells. METHODS We investigated the inhibitory effects of natsudaidain, which is a polymethoxyflavone isolated from Citrus plants, on histamine release, tumour necrosis factor-alpha production and cyclooxygenase-2 expression in Ca ionophore-stimulated rat basophilic leukemia cells (A23187-stimulated RBL-2H3 cells) by spectrofluorometric, ELISA and immunoblotting methods. KEY FINDINGS The percent of histamine release from A23187-stimulated RBL-2H3 cells pretreated with natsudaidain at 5, 25 and 50 microM was not changed as compared with non-treated A23187-stimulated cells. At 100 and 200 microM, natsudaidain pretreatment resulted in slightly reduced histamine release (% histamine release, 89.8+/-3.5% and 71.5+/-5.6% at 100 and 200 microM). Thus, natsudaidain hardly affects histamine release from RBL-2H3 cells, except at high concentrations. On the other hand, natsudaidain dose-dependently inhibited tumour necrosis factor-alpha protein and mRNA levels in A23187-stimulated RBL-2H3 cells; a concentration of 6.8 microM was required for a 50% reduction. In addition, all concentrations of this compound that we tested also inhibited cyclooxygenase-2 protein expression. The mRNA levels of cyclooxygenase-2 in A23187-stimulated RBL-2H3 cells treated with natsudaidain were also markedly decreased. The phosphorylated-p38 MAPK protein levels in A23187-stimulated RBL-2H3 cells treated with natsudaidain were lower than in the non-treated cells. CONCLUSIONS These findings suggest that natsudaidain inhibits tumour necrosis factor-alpha and cyclooxygenase-2 production by suppressing p38 MAPK phosphorylation but not p65 NFkappaB phosphorylation, and that natsudaidain might alleviate inflammatory diseases.
柑桔纳屈苷对RBL-2H3细胞tnf - α和环氧合酶-2表达的影响
目的:黄酮类化合物抑制肥大细胞释放的化学介质的活性。我们的目的是研究从柑橘植物中分离的多甲氧基黄酮natsudaidain对肥大细胞的影响。方法采用荧光光谱法、酶联免疫吸附法和免疫印迹法研究了从柑橘类植物中分离的多甲氧基黄酮纳屈苷对Ca离子载体刺激的大鼠嗜碱性白血病细胞(a23187刺激的RBL-2H3细胞)组胺释放、肿瘤坏死因子α产生和环氧化酶-2表达的抑制作用。与未处理a23187刺激的细胞相比,用那舒地丹在5、25和50微米下预处理a23187刺激的RBL-2H3细胞的组胺释放百分比没有变化。在100和200微米时,纳舒地丹预处理导致组胺释放量略有降低(组胺释放%,100和200微米时分别为89.8+/-3.5%和71.5+/-5.6%)。因此,除了高浓度外,那舒地丹几乎不影响RBL-2H3细胞的组胺释放。另一方面,那舒地丹剂量依赖性地抑制a23187刺激的RBL-2H3细胞中的肿瘤坏死因子- α蛋白和mRNA水平;需要6.8微米的浓度才能减少50%。此外,我们测试的所有浓度的化合物也抑制环氧化酶-2蛋白的表达。纳舒地丹对a23187刺激RBL-2H3细胞的环氧化酶-2 mRNA水平也显著降低。在a23187刺激的RBL-2H3细胞中,纳苏地丹处理的磷酸化p38 MAPK蛋白水平低于未处理的细胞。结论纳他丹通过抑制p38 MAPK磷酸化而非p65 NFkappaB磷酸化抑制肿瘤坏死因子- α和环氧化酶-2的产生,提示纳他丹可能具有减轻炎性疾病的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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