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DA-6034,一种黄酮类衍生物,可预防和改善葡聚糖硫酸钠诱导的结肠炎,并抑制结肠癌发生。

DA-6034, a derivative of flavonoid, prevents and ameliorates dextran sulfate sodium-induced colitis and inhibits colon carcinogenesis.

作者信息

Nam Su Youn, Kim Joo Sung, Kim Jung Mogg, Lee Jong Yeul, Kim Nayoung, Jung Hyun Chae, Song In Sung

机构信息

Center for Cancer Prevention and Detection, National Cancer Center, Goyang, Korea.

出版信息

Exp Biol Med (Maywood). 2008 Feb;233(2):180-91. doi: 10.3181/0707-RM-186.

Abstract

Previously, we have shown that DA-6034, a synthetic derivative of flavonoid eupatilin, inhibited NF-kappaB activation in colon epithelial cells and prevented trinitrobenzene sulfonic acid-induced rat colitis. The aim of this study was to investigate the preventive and therapeutic effect of DA-6034 on dextran sulfate sodium (DSS)-induced colitis and on inflammation-related cancer. C57BL/6 mice were given 4% DSS for 5 days with and without DA-6034 in the acute preventive model. In the acute therapeutic model, mice were given 4% DSS for 5 days followed by rectal administration of DA-6034. Colitis was quantified by body weight, disease activity index (DAI), colon length, and histology. In the inflammation-related cancer model, mice were given a single intraperitoneal injection of azoxymethane, then three cycles of 2% DSS for 5 days, then 2 weeks of free water consumption. Apoptosis was determined by in situ terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling assay, and the expression of Ki-67, phospho-kappaB kinase alpha (IKKalpha), and COX-2 were evaluated by immunohistochemistry. In both the acute preventive and acute therapeutic models, DA-6034 significantly attenuated DSS-induced weight loss, an increase in DAI, and a shortening of colon length. DA-6034-treated mice maintained crypt architecture and revealed a scanty infiltration of inflammatory cells in both the preventive and therapeutic models. In the inflammation-related cancer model, DA-6034 reduced the number of colon tumors and ameliorated weight loss and shortening of colon length. DA-6034 strongly enhanced apoptosis and inhibited the expression of COX-2 and phospho-IKKalpha in inflammation-related colon cancer models. Our results suggest that DA-6034 prevents acute murine colitis and inhibits inflammation-related colon carcinogenesis. DA-6034 could be a potential therapeutic agent for inflammatory bowel disease.

摘要

此前,我们已经表明,黄酮类化合物灯盏乙素的合成衍生物DA-6034可抑制结肠上皮细胞中的核因子-κB激活,并预防三硝基苯磺酸诱导的大鼠结肠炎。本研究的目的是调查DA-6034对葡聚糖硫酸钠(DSS)诱导的结肠炎以及炎症相关癌症的预防和治疗作用。在急性预防模型中,给C57BL/6小鼠喂食4% DSS 5天,同时或不给予DA-6034。在急性治疗模型中,给小鼠喂食4% DSS 5天,然后直肠给予DA-6034。通过体重、疾病活动指数(DAI)、结肠长度和组织学对结肠炎进行量化。在炎症相关癌症模型中,给小鼠单次腹腔注射氧化偶氮甲烷,然后三个周期的2% DSS处理5天,然后自由饮水2周。通过原位末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记法测定细胞凋亡,并通过免疫组织化学评估Ki-67、磷酸化核因子-κB激酶α(IKKα)和环氧化酶-2(COX-2)的表达。在急性预防和急性治疗模型中,DA-6034均显著减轻了DSS诱导的体重减轻、DAI增加和结肠长度缩短。在预防和治疗模型中,接受DA-6034治疗的小鼠维持了隐窝结构,且炎症细胞浸润较少。在炎症相关癌症模型中,DA-6034减少了结肠肿瘤的数量,并改善了体重减轻和结肠长度缩短的情况。在炎症相关结肠癌模型中,DA-6034强烈增强了细胞凋亡,并抑制了COX-2和磷酸化IKKα的表达。我们的结果表明,DA-6034可预防急性小鼠结肠炎,并抑制炎症相关的结肠癌发生。DA-6034可能是一种治疗炎症性肠病的潜在治疗药物。

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