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桃红四物汤对肺癌合并慢性阻塞性肺疾病小鼠的抗炎作用

Anti-inflammatory effects of Tao Hong Si Wu Tang in mice with lung cancer and chronic obstructive pulmonary disease.

作者信息

Wang Guo-Li, Xu Yan-Ling, Zhao Ke-Ming, Sui Ai-Feng, Wang Li-Na, Deng Hu, Wang Ge

机构信息

First Department of Respiratory and Critical Care Medicine/Pulmonary Disease, The First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang 110000, Liaoning Province, China.

Second Department of Respiratory and Critical Care Medicine/Pulmonary Disease, The First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang 110000, Liaoning Province, China.

出版信息

World J Clin Oncol. 2024 Sep 24;15(9):1198-1206. doi: 10.5306/wjco.v15.i9.1198.

DOI:10.5306/wjco.v15.i9.1198
PMID:39351459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11438842/
Abstract

BACKGROUND

Lung cancer (LC) combined with chronic obstructive pulmonary disease (COPD) is a common combination of comorbidities. Anti-inflammation and modulation of oxidative/antioxidative imbalance may prevent COPD-induced LC, and are also crucial to the treatment of LC combined with COPD. Modern studies have shown that Tao Hong Si Wu Tang (THSW) has vasodilatory, anti-inflammatory, anti-fatigue, anti-shock, immunoregulatory, lipid-reducing, micronutrient-supplementing, and anti-allergy effects.

AIM

To observe the effects of THSW on COPD and LC in mice.

METHODS

A total of 100 specific pathogen-free C57/BL6 mice were randomly divided into five groups: Blank control group (group A), model control group (group B), THSW group (group C), IL-6 group (group D), and THSW + IL-6 group (group E), with 20 mice in each group. A COPD mouse model was established using fumigation plus lipopolysaccharide intra-airway drip, and an LC model was replicated by inoculation using the Lewis cell method.

RESULTS

The blank control group exhibited a clear alveolar structure. The model control and IL-6 groups had thickened alveolar walls, with smaller alveolar lumens, interstitial edema, and several inflammatory infiltrating cells. Histopathological changes in the lungs of the THSW and THSW + IL-6 groups were less than those of the model control group. The serum IL-1β, IL-6, and TNF-α levels and IL-6R, JAK, p-JAK, STAT1/3, p-STAT1/3, FOXO, p-FOXO, and IL-7R expression levels in lung tissues of mice in the rest of the groups were significantly higher than those of the blank control group ( < 0.01). Compared with the model control group, the IL-6 group demonstrated significantly higher levels for the abovementioned proteins in the serum and lung tissues ( < 0.01), and the THSW group had significantly higher serum IL-1β, IL-6, and TNF-α levels and IL-7R expression levels in lung tissues ( < 0.01) but significantly decreased IL-6R, JAK, p-JAK, STAT1/3, p-STAT1/3, FOXO, p-FOXO, and IL-7R levels ( < 0.01).

CONCLUSION

THSW reduces the serum IL-1β, IL-6, and TNF-α levels in the mouse model with anti-inflammatory effects. Its anti-inflammatory mechanism lies in inhibiting the overactivation of the JAK/STAT1/3 signaling pathway.

摘要

背景

肺癌(LC)合并慢性阻塞性肺疾病(COPD)是常见的共病组合。抗炎及调节氧化/抗氧化失衡可能预防COPD诱发的LC,对LC合并COPD的治疗也至关重要。现代研究表明,桃红四物汤(THSW)具有血管舒张、抗炎、抗疲劳、抗休克、免疫调节、降脂、补充微量营养素及抗过敏作用。

目的

观察THSW对小鼠COPD和LC的影响。

方法

将100只无特定病原体的C57/BL6小鼠随机分为五组:空白对照组(A组)、模型对照组(B组)、THSW组(C组)、IL-6组(D组)和THSW + IL-6组(E组),每组20只。采用烟熏加气道内滴注脂多糖建立COPD小鼠模型,用Lewis细胞法接种复制LC模型。

结果

空白对照组肺泡结构清晰。模型对照组和IL-6组肺泡壁增厚,肺泡腔变小,间质水肿,有多处炎性浸润细胞。THSW组和THSW + IL-6组小鼠肺组织的组织病理学变化小于模型对照组。其余各组小鼠血清IL-1β、IL-6和TNF-α水平以及肺组织中IL-6R、JAK、p-JAK、STAT1/3、p-STAT1/3、FOXO、p-FOXO和IL-7R表达水平均显著高于空白对照组(P < 0.01)。与模型对照组相比,IL-6组血清和肺组织中上述蛋白水平显著更高(P < 0.01),THSW组血清IL-1β、IL-6和TNF-α水平以及肺组织中IL-7R表达水平显著更高(P < 0.01),但IL-6R、JAK、p-JAK、STAT1/3、p-STAT1/3、FOXO、p-FOXO和IL-7R水平显著降低(P < 0.01)。

结论

THSW降低小鼠模型血清IL-1β、IL-6和TNF-α水平,具有抗炎作用。其抗炎机制在于抑制JAK/STAT1/3信号通路的过度激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/003a924a5b42/WJCO-15-1198-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/49d444600709/WJCO-15-1198-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/80f8abc8538e/WJCO-15-1198-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/df6e6a801ee7/WJCO-15-1198-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/1035b7bd166f/WJCO-15-1198-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/003a924a5b42/WJCO-15-1198-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/49d444600709/WJCO-15-1198-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/80f8abc8538e/WJCO-15-1198-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/df6e6a801ee7/WJCO-15-1198-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/1035b7bd166f/WJCO-15-1198-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165e/11438842/003a924a5b42/WJCO-15-1198-g005.jpg

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