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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Bu-Shen-Fang-Chuan formula attenuates T-lymphocytes recruitment in the lung of rats with COPD through suppressing CXCL9/CXCL10/CXCL11-CXCR3 axis
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Bu-Shen-Fang-Chuan formula attenuates T-lymphocytes recruitment in the lung of rats with COPD through suppressing CXCL9/CXCL10/CXCL11-CXCR3 axis

机译:Bu-Shen-Fang-Chuan公式通过抑制CXCL9 / CXCL10 / CXCL11-CXCR3轴抑制COPD的大鼠肺部的T淋巴细胞募集

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摘要

Chronic obstructive pulmonary disease (COPD) is a common respiratory disease characterized by irreversible airflow limitation. The current medications show limited effects on the decline of pulmonary function in COPD. Our multicenter clinical trial found that Bu-Shen-Fang-Chuan fomula (BSFCF), a Chinese herbal formula, markedly reduced the frequencies of acute exacerbation of COPD and delayed lung function decline. However, the underlying mechanisms are still unclear. In this study, we established a COPD rat model through a 6-month exposure to cigarette smoke (CS) and found that BSFCF (7.2 g/kg) effectively improved CS-induced reduction in pulmonary function and remarkably decreased the numbers of inflammatory cells in bronchoalveolar lavage fluid (BALF). Importantly, BSFCF treatment notably prevented the accumulation of T-lymphocytes (especially CD8(+) T-cells) in the lung of COPD rats. RNA sequencing analysis of lung tissue demonstrated that CXCL9/CXCL10/CXCL11-CXCR3 chemokine axis in the lung of CS-exposed rats was significantly suppressed by BSFCF. Moreover, our Real-time PCR data verified that BSFCF evidently inhibited the mRNA expressions of CXCL9, CXCL10, CXCL11 and CXCR3. Conclusively, BSFCF markedly improved pulmonary function and attenuated CD8(+) T-cells recruitment in the lung of CS-exposed rats, which were partially through inhibition of CXCL9/CXCL10/CXCL11-CXCR3 axis.
机译:慢性阻塞性肺病(COPD)是一种常见的呼吸道疾病,其特征是不可逆转的气流限制。目前的药物对COPD肺功能下降的影响有限。我们的多中心临床试验发现,Bu-Shen-Fang-Chuan Fomula(BSFCF),中草原,显着降低了COPD急性加剧的频率,延迟肺功能下降。但是,潜在机制仍然不清楚。在这项研究中,我们通过6个月暴露于香烟烟雾(CS)建立了一种COPD大鼠模型,发现BSFCF(7.2g / kg)有效地改善了肺功能的CS诱导的降低,并且显着降低了炎症细胞的数量支气管肺泡灌洗液(BALF)。重要的是,BSFCF治疗尤利地阻止了T淋巴细胞的积累(特别是CD8(+)T细胞)在COPD大鼠的肺中。肺组织的RNA测序分析证明了CSFCF的CS暴露大鼠肺中的CXCL9 / CXCL10 / CXCL11-CXCR3趋化轴显着抑制了CSFCF。此外,我们的实时PCR数据证明了BSFCF明显抑制CXCL9,CXCL10,CXCL11和CXCR3的mRNA表达。结论,BSFCF明显改善了肺功能和减毒的CS-曝光大鼠肺部的肺功能和减毒的CD8(+)T细胞,其部分通过抑制CXC19 / CXCL10 / CXCL11-CXCR3轴。

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  • 作者单位

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

    Fudan Univ Huashan Hosp Dept Integrat Med Shanghai 200040 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

    BSFCF; COPD; T-cells; CD8; CXCR3;

    机译:BSFCF;COPD;T细胞;CD8;CXCR3;

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