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樗树通过抑制核因子-κB 的激活发挥抗过敏性作用,并抑制炎症细胞因子的表达。

Ailanthus altissima swingle has anti-anaphylactic effect and inhibits inflammatory cytokine expression via suppression of nuclear factor-kappaB activation.

机构信息

Cancer Preventive Material Development Research Center, Department of Pharmacology, Institute of Oriental Medicine, College of Oriental Medicine, Kyung Hee University, Kyung Hee, South Korea.

出版信息

In Vitro Cell Dev Biol Anim. 2010 Jan;46(1):72-81. doi: 10.1007/s11626-009-9237-y. Epub 2009 Sep 30.

Abstract

Ailanthus altissima swingle (ailanthic cortex, AAS) has been used as a traditional medicine for fever, bleeding, infection, and inflammation for many years in Korea. However, its mechanisms have not been examined. In the present study, we investigate the effect of AAS on the mast-cell-mediated allergic and inflammatory reaction using in vivo and in vitro models and elucidate its molecular mechanisms. AAS significantly inhibited compound 48/48-induced edema and systemic anaphylaxis. AAS significantly inhibited passive cutaneous anaphylaxis. AAS inhibited histamine release from rat peritoneal mast cells (RPMCs) in a dose-dependent manner. Moreover, AAS significantly inhibited production of inflammatory cytokines, tumor necrosis factor (TNF), interleukin (IL)-6, and IL-8 on the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated human mast cell line, HMC-1 cells. AAS inhibits the IgE or stem cell factor-induced TNF production on RPMCs. In activated HMC-1 cells, the expression level of NF-kappaB/Rel A protein increased in the nucleus, whereas the level of NF-kappaB/Rel A in the nucleus was decreased by AAS treatment. In addition, AAS inhibited the PMACI-induced IkappaBalpha degradation. In conclusion, the present results indicate that AAS has potent anti-anaphylactic and anti-inflammatory properties.

摘要

樗树白皮(樗皮,AAS)多年来一直被用作韩国的传统药物,用于治疗发热、出血、感染和炎症。然而,其机制尚未得到检验。在本研究中,我们使用体内和体外模型研究了 AAS 对肥大细胞介导的过敏和炎症反应的影响,并阐明了其分子机制。AAS 显著抑制了化合物 48/48 诱导的水肿和全身性过敏反应。AAS 显著抑制被动皮肤过敏反应。AAS 以剂量依赖的方式抑制大鼠腹腔肥大细胞(RPMC)中的组胺释放。此外,AAS 显著抑制了佛波醇 12-肉豆蔻酸 13-乙酸酯和钙离子载体 A23187(PMACI)刺激的人肥大细胞系 HMC-1 细胞中炎症细胞因子肿瘤坏死因子(TNF)、白细胞介素(IL)-6 和 IL-8 的产生。AAS 抑制 RPMC 上 IgE 或干细胞因子诱导的 TNF 产生。在活化的 HMC-1 细胞中,NF-kappaB/Rel A 蛋白的表达水平在核内增加,而 AAS 处理后核内的 NF-kappaB/Rel A 水平降低。此外,AAS 抑制了 PMACI 诱导的 IkappaBalpha 降解。总之,本研究结果表明 AAS 具有较强的抗过敏和抗炎特性。

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