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姜黄素可减轻细胞培养物和小鼠中幽门螺杆菌感染根除过程中基质金属蛋白酶-3 和 -9 的活性。

Curcumin alleviates matrix metalloproteinase-3 and -9 activities during eradication of Helicobacter pylori infection in cultured cells and mice.

机构信息

Indian Institute of Chemical Biology, Kolkata, India.

出版信息

PLoS One. 2011 Jan 21;6(1):e16306. doi: 10.1371/journal.pone.0016306.

DOI:10.1371/journal.pone.0016306
PMID:21283694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3025008/
Abstract

Current therapy-regimens against Helicobacter pylori (Hp) infections have considerable failure rates and adverse side effects that urge the quest for an effective alternative therapy. We have shown that curcumin is capable of eradicating Hp-infection in mice. Here we examine the mechanism by which curcumin protects Hp infection in cultured cells and mice. Since, MMP-3 and -9 are inflammatory molecules associated to the pathogenesis of Hp-infection, we investigated the role of curcumin on inflammatory MMPs as well as proinflammatory molecules. Curcumin dose dependently suppressed MMP-3 and -9 expression in Hp infected human gastric epithelial (AGS) cells. Consistently, Hp-eradication by curcumin-therapy involved significant downregulation of MMP-3 and -9 activities and expression in both cytotoxic associated gene (cag)(+ve) and cag(-ve) Hp-infected mouse gastric tissues. Moreover, we demonstrate that the conventional triple therapy (TT) alleviated MMP-3 and -9 activities less efficiently than curcumin and curcumin's action on MMPs was linked to decreased pro-inflammatory molecules and activator protein-1 activation in Hp-infected gastric tissues. Although both curcumin and TT were associated with MMP-3 and -9 downregulation during Hp-eradication, but unlike TT, curcumin enhanced peroxisome proliferator-activated receptor-γ and inhibitor of kappa B-α. These data indicate that curcumin-mediated healing of Hp-infection involves regulation of MMP-3 and -9 activities.

摘要

目前针对幽门螺杆菌 (Hp) 感染的治疗方案存在相当高的失败率和不良反应,这促使人们寻求有效的替代疗法。我们已经证明姜黄素能够根除小鼠的 Hp 感染。在这里,我们研究了姜黄素在培养细胞和小鼠中保护 Hp 感染的机制。由于 MMP-3 和 MMP-9 是与 Hp 感染发病机制相关的炎症分子,我们研究了姜黄素对炎症 MMPs 以及促炎分子的作用。姜黄素呈剂量依赖性抑制 Hp 感染的人胃上皮 (AGS) 细胞中 MMP-3 和 MMP-9 的表达。一致地,姜黄素治疗根除 Hp 感染涉及 MMP-3 和 MMP-9 活性和表达的显著下调,这在细胞毒性相关基因 (cag)(+ve) 和 cag(-ve) Hp 感染的小鼠胃组织中均有体现。此外,我们证明传统三联疗法 (TT) 缓解 MMP-3 和 MMP-9 活性的效果不如姜黄素,并且姜黄素对 MMPs 的作用与 Hp 感染胃组织中促炎分子和激活蛋白-1 激活的减少有关。虽然姜黄素和 TT 在根除 Hp 感染期间均与 MMP-3 和 MMP-9 的下调有关,但与 TT 不同的是,姜黄素增强了过氧化物酶体增殖物激活受体-γ 和κB 抑制物-α。这些数据表明,姜黄素介导的 Hp 感染的愈合涉及 MMP-3 和 MMP-9 活性的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/781bc5514ba6/pone.0016306.g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/781bc5514ba6/pone.0016306.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/0d26fb9d6553/pone.0016306.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/9cbc8e2f293e/pone.0016306.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/6d58a366840c/pone.0016306.g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/9541740d779b/pone.0016306.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f79/3025008/781bc5514ba6/pone.0016306.g007.jpg

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