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白术内酯III对TSLP诱导的肥大细胞增殖的改善作用。

Ameliorative effect of atractylenolide III in the mast cell proliferation induced by TSLP.

作者信息

Yoou Myoung-Schook, Nam Sun-Young, Jin Mu Hyun, Lee So Young, Kim Mi-Sun, Roh Seok Seon, Choi In Hwa, Woo Nariyah, Lim SeokWon, Kim Dong Hyun, Jang Jae-Bum, Kim Hyung-Min, Jeong Hyun-Ja

机构信息

Department of Pharmacology, College of Korean Medicine, Kyung Hee University, 26, Kyungheedae-ro, Dongdaemun-gu, Seoul, 02447, Republic of Korea.

Skin Research Center, Research Park, LG Household & Healthcare Ltd., 175, Gajeong-ro, Yuseong-gu, Daejeon, 34114, Republic of Korea.

出版信息

Food Chem Toxicol. 2017 Aug;106(Pt A):78-85. doi: 10.1016/j.fct.2017.05.042. Epub 2017 May 22.

Abstract

Atractylenolide III (ATL-III) is an active compound of Atractylodes lancea, which has been widely used for the treatment of cancer. Cancer is closely connected with inflammation, and many anti-inflammatory agents are also used to treat cancer. We investigated the influence of ATL-III on thymic stromal lymphopoietin (TSLP)-induced inflammatory reactions. Pretreatment with ATL-III suppressed murine double minute 2 levels and promoted p53 levels in TSLP-treated human mast cell, HMC-1 cells. Mast cell proliferation increased by TSLP or IL-3 stimulation was significantly decreased by ATL-III pretreatment. Interleukin (IL)-13 and phosphorylated signal transducer and activator of transcription 3, 5, and 6 levels in TSLP-treated HMC-1 cells were also decreased by ATL-III pretreatment. In addition, ATL-III decreased the TSLP-induced production of proinflammatory cytokines (IL-6, IL-1β, tumor necrosis factor-α, and IL-8). ATL-III decreased the levels of Bcl2 and procaspase-3 and increased caspase-3 activation and cleaved PARP levels. Furthermore, ATL-III decreased TSLP-induced mast cell proliferation and the production of inflammatory cytokine by LAD2 cells. Taken together, these findings suggest that ATL-III plays a useful role as an anti-inflammatory agent and should be viewed as a potential anti-cancer agent.

摘要

白术内酯III(ATL-III)是白术的一种活性化合物,已被广泛用于癌症治疗。癌症与炎症密切相关,许多抗炎剂也用于治疗癌症。我们研究了ATL-III对胸腺基质淋巴细胞生成素(TSLP)诱导的炎症反应的影响。用ATL-III预处理可抑制TSLP处理的人肥大细胞HMC-1细胞中鼠双微体2水平并提高p53水平。ATL-III预处理可显著降低TSLP或IL-3刺激引起的肥大细胞增殖。ATL-III预处理还可降低TSLP处理的HMC-1细胞中白细胞介素(IL)-13以及磷酸化的信号转导和转录激活因子3、5和6的水平。此外,ATL-III可降低TSLP诱导的促炎细胞因子(IL-6、IL-1β、肿瘤坏死因子-α和IL-8)的产生。ATL-III降低了Bcl2和procaspase-3的水平,增加了caspase-3的激活和PARP裂解水平。此外,ATL-III降低了TSLP诱导的LAD2细胞肥大细胞增殖和炎性细胞因子的产生。综上所述,这些发现表明ATL-III作为一种抗炎剂发挥着有益作用,应被视为一种潜在的抗癌剂。

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