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绿茶提取物可改善香烟冷凝物诱导的慢性阻塞性肺疾病中巨噬细胞驱动的肺气肿病变。

Green tea extract ameliorates macrophage-driven emphysematous lesions in chronic obstructive pulmonary disease induced by cigarette smoke condensate.

机构信息

College of Veterinary Medicine (BK21 FOUR Program), Chungnam National University, Daejeon, Republic of Korea.

出版信息

Phytother Res. 2023 Apr;37(4):1366-1376. doi: 10.1002/ptr.7745. Epub 2023 Feb 2.

Abstract

Chronic obstructive pulmonary disease (COPD) is an important lung disease characterized by complicated symptoms including emphysema. We aimed to explore the mechanisms underlying the protective effect of green tea extract (GTE) on cigarette smoke condensate (CSC)-induced emphysema by demonstrating the reduction of macrophage-induced protease expression through GTE treatment in vivo and in vitro. Mice were intranasally administered 50 mg/kg CSC once a week for 4 weeks, and doses of 100 or 300 mg/kg GTE were administered orally once daily for 4 weeks. GTE significantly reduced macrophage counts in bronchoalveolar lavage fluid and emphysematous lesions in lung tissues in CSC-exposed mice. In addition, GTE suppressed CSC-induced extracellular signal-regulated kinase (ERK)/activator protein (AP)-1 phosphorylation followed by matrix metalloproteinases (MMP)-9 expression as revealed by western blotting, immunohistochemistry, and zymography in CSC-instilled mice. These underlying mechanisms related to reduced protease expression were confirmed in NCI-H292 cells stimulated by CSC. Taken together, GTE effectively inhibits macrophage-driven emphysematous lesions induced by CSC treatment, and these protective effects of GTE are closely related to the ERK/AP-1 signaling pathway, followed by a reduced protease/antiprotease imbalance. These results suggest that GTE can be used as a supplementary agent for the prevention of emphysema progression in COPD patients.

摘要

慢性阻塞性肺疾病(COPD)是一种重要的肺部疾病,其特征为包括肺气肿在内的复杂症状。我们旨在通过体内和体外实验证明绿茶提取物(GTE)通过降低巨噬细胞诱导的蛋白酶表达来探究 GTE 对香烟烟雾冷凝物(CSC)诱导的肺气肿的保护作用机制。每周一次通过鼻腔给予小鼠 50mg/kg 的 CSC,共 4 周,同时给予 100 或 300mg/kg 的 GTE 进行口服处理,共 4 周。GTE 可显著降低 CSC 暴露小鼠的支气管肺泡灌洗液中的巨噬细胞计数和肺组织中的肺气肿病变。此外,GTE 可抑制 CSC 诱导的细胞外信号调节激酶(ERK)/激活蛋白(AP)-1 磷酸化,随后通过 Western blot、免疫组织化学和明胶酶谱法在 CSC 灌注小鼠中抑制基质金属蛋白酶(MMP)-9 的表达。这些与降低蛋白酶表达相关的潜在机制在 CSC 刺激的 NCI-H292 细胞中得到了证实。总之,GTE 可有效抑制 CSC 处理引起的巨噬细胞驱动的肺气肿病变,而 GTE 的这些保护作用与 ERK/AP-1 信号通路密切相关,随后是蛋白酶/抗蛋白酶失衡的减少。这些结果表明,GTE 可用作 COPD 患者预防肺气肿进展的辅助剂。

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