• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

芩暴红止咳口服液通过抑制 OLFM4 减轻 LPS 诱导的幼鼠急性肺损伤

Qinbaohong Zhike Oral Liquid Attenuates LPS-Induced Acute Lung Injury in Immature Rats by Inhibiting OLFM4.

机构信息

Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.

Tianjin University of Traditional Chinese Medicine, Tianjin, China.

出版信息

Oxid Med Cell Longev. 2022 Aug 16;2022:7272371. doi: 10.1155/2022/7272371. eCollection 2022.

DOI:10.1155/2022/7272371
PMID:36035204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9400428/
Abstract

Acute respiratory infections (ARIs) are a common public safety threat with high morbidity and mortality in pediatric patients worldwide. Qinbaohong Zhike oral liquid (QBH), a marketed traditional Chinese medicine product, has been widely used to cure respiratory diseases. QBH is reported to have antitussive, expectorant, and antiasthmatic properties. However, its treatment effect against ARIs is not elucidated. This study aimed to explore the therapeutic efficacy of QBH in the treatment of ARIs-induced pneumonia. Network pharmacology was used to predict the possible targets of QBH against ARIs. Next, the tracheal lipopolysaccharide (LPS-)-induced acute lung injury (ALI) immature rat model was constructed to evaluate the therapeutic effect of QBH. Tandem mass tag (TMT-)-based quantitative proteomics was then used to screen the in-depth disease targets of QBH. QBH exerted a protective effect against LPS-induced ALI by inhibiting pulmonary pathological damage. QBH also reduced the levels of interleukin (IL)-6, tumor necrosis factor (TNF)-, interferon (IFN)-, and granulocyte macrophage colony-stimulating factor (GM-CSF) in the serum and IL-1, IL-6, IL-8, TNF-, IFN-, and GM-CSF in the lung tissue. Based on proteomic data, olfactomedin 4 (OLFM4) related to immunity and inflammation was selected as a potential target. Western blot analysis further confirmed the moderating effect of QBH downregulation on OLFM4 in the lung tissue. Our findings demonstrated that QBH alleviated lung tissue damage and inflammatory reaction via inhibiting OLFM4 expression in LPS-challenged immature rats. Our research indicates that QBH may have therapeutic potential for treating ARIs-related ALI in pediatric patients, which also serves as a candidate target for drug therapy of ALI by intervening OLFM-related signaling pathways.

摘要

急性呼吸道感染(ARI)是一种常见的公共安全威胁,在全球儿科患者中具有高发病率和死亡率。秦巴宏止咳口服液(QBH)是一种市售的中药产品,已广泛用于治疗呼吸道疾病。QBH 具有镇咳、祛痰和抗哮喘作用。然而,其治疗 ARI 的效果尚不清楚。本研究旨在探讨 QBH 治疗 ARI 引起的肺炎的疗效。网络药理学用于预测 QBH 治疗 ARI 的可能靶点。接下来,构建了气管脂多糖(LPS)-诱导的急性肺损伤(ALI)未成熟大鼠模型,以评估 QBH 的治疗效果。然后,使用串联质量标签(TMT)-基于定量蛋白质组学筛选 QBH 的深入疾病靶点。QBH 通过抑制肺病理损伤对 LPS 诱导的 ALI 发挥保护作用。QBH 还降低了血清中白细胞介素(IL)-6、肿瘤坏死因子(TNF)-、干扰素(IFN)-和粒细胞巨噬细胞集落刺激因子(GM-CSF)以及肺组织中 IL-1、IL-6、IL-8、TNF-、IFN-和 GM-CSF 的水平。基于蛋白质组学数据,选择与免疫和炎症相关的嗅觉素 4(OLFM4)作为潜在靶点。Western blot 分析进一步证实了 QBH 下调对肺组织中 OLFM4 的调节作用。我们的研究结果表明,QBH 通过抑制 LPS 刺激的未成熟大鼠肺组织中 OLFM4 的表达来减轻肺组织损伤和炎症反应。我们的研究表明,QBH 可能对治疗儿科患者 ARI 相关 ALI 具有治疗潜力,这也为通过干预 OLFM 相关信号通路治疗 ALI 的药物治疗提供了候选靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/17da7f5c19d1/OMCL2022-7272371.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/79467ac29b90/OMCL2022-7272371.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/bd6720b6f4f8/OMCL2022-7272371.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/f897e88958e5/OMCL2022-7272371.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/b138d32b52e6/OMCL2022-7272371.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/09dc6bfb0760/OMCL2022-7272371.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/17da7f5c19d1/OMCL2022-7272371.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/79467ac29b90/OMCL2022-7272371.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/bd6720b6f4f8/OMCL2022-7272371.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/f897e88958e5/OMCL2022-7272371.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/b138d32b52e6/OMCL2022-7272371.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/09dc6bfb0760/OMCL2022-7272371.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65e/9400428/17da7f5c19d1/OMCL2022-7272371.006.jpg

相似文献

1
Qinbaohong Zhike Oral Liquid Attenuates LPS-Induced Acute Lung Injury in Immature Rats by Inhibiting OLFM4.芩暴红止咳口服液通过抑制 OLFM4 减轻 LPS 诱导的幼鼠急性肺损伤
Oxid Med Cell Longev. 2022 Aug 16;2022:7272371. doi: 10.1155/2022/7272371. eCollection 2022.
2
Huashibaidu formula attenuates sepsis-induced acute lung injury via suppressing cytokine storm: Implications for treatment of COVID-19.化湿败毒方通过抑制细胞因子风暴减轻脓毒症诱导的急性肺损伤:治疗 COVID-19 的意义。
Phytomedicine. 2023 Jan;109:154549. doi: 10.1016/j.phymed.2022.154549. Epub 2022 Nov 19.
3
Multiple anti-inflammatory mechanisms of Zedoary Turmeric Oil Injection against lipopolysaccharides-induced acute lung injury in rats elucidated by network pharmacology combined with transcriptomics.网络药理学结合转录组学阐明莪术油注射液抗脂多糖诱导大鼠急性肺损伤的多重抗炎机制。
Phytomedicine. 2022 Nov;106:154418. doi: 10.1016/j.phymed.2022.154418. Epub 2022 Aug 31.
4
JFNE-A isolated from Jing-Fang n-butanol extract attenuates lipopolysaccharide-induced acute lung injury by inhibiting oxidative stress and the NF-κB signaling pathway via promotion of autophagy.从京方正丁醇提取物中分离得到的 JFNE-A 通过促进自噬来抑制氧化应激和 NF-κB 信号通路,从而减轻脂多糖诱导的急性肺损伤。
Phytomedicine. 2022 Feb;96:153891. doi: 10.1016/j.phymed.2021.153891. Epub 2021 Dec 20.
5
Granulocyte macrophage-colony stimulating factor (GM-CSF) augments acute lung injury via its neutrophil priming effects.粒细胞巨噬细胞集落刺激因子(GM-CSF)通过其对中性粒细胞的预激作用加重急性肺损伤。
J Korean Med Sci. 2008 Apr;23(2):288-95. doi: 10.3346/jkms.2008.23.2.288.
6
Shema Oral Liquid Ameliorates the Severity of LPS-Induced COPD Regulating DNMT1.舍曲林口服液通过调节DNMT1改善脂多糖诱导的慢性阻塞性肺疾病的严重程度。
Front Pharmacol. 2022 Jun 8;13:903593. doi: 10.3389/fphar.2022.903593. eCollection 2022.
7
Qingwenzhike Prescription Alleviates Acute Lung Injury Induced by LPS Inhibiting TLR4/NF-kB Pathway and NLRP3 Inflammasome Activation.清瘟止咳方通过抑制TLR4/NF-κB通路和NLRP3炎性小体激活减轻脂多糖诱导的急性肺损伤。
Front Pharmacol. 2021 Dec 23;12:790072. doi: 10.3389/fphar.2021.790072. eCollection 2021.
8
Upregulation of claudin‑4 by Chinese traditional medicine Shenfu attenuates lung tissue damage by acute lung injury aggravated by acute gastrointestinal injury.中药参附上调 Claudin-4 表达减轻急性胃肠损伤加重急性肺损伤的肺组织损伤
Pharm Biol. 2022 Dec;60(1):1981-1993. doi: 10.1080/13880209.2022.2128824.
9
Granulocyte-macrophage colony-stimulating factor amplification of interleukin-1beta and tumor necrosis factor alpha production in THP-1 human monocytic cells stimulated with lipopolysaccharide of oral microorganisms.粒细胞-巨噬细胞集落刺激因子增强经口腔微生物脂多糖刺激的THP-1人单核细胞中白细胞介素-1β和肿瘤坏死因子α的产生。
Clin Diagn Lab Immunol. 1998 May;5(3):341-7. doi: 10.1128/CDLI.5.3.341-347.1998.
10
Protectin DX Exhibits Protective Effects in Mouse Model of Lipopolysaccharide-Induced Acute Lung Injury.保护素 DX 在脂多糖诱导的急性肺损伤小鼠模型中具有保护作用。
Chin Med J (Engl). 2018 May 20;131(10):1167-1173. doi: 10.4103/0366-6999.227618.

引用本文的文献

1
Tetramethylpyrazine mitigates lipopolysaccharide-induced acute lung injury by inhibiting the HMGB1/TLR4/NF-κB signaling pathway in mice.川芎嗪通过抑制小鼠HMGB1/TLR4/NF-κB信号通路减轻脂多糖诱导的急性肺损伤。
J Thorac Dis. 2025 Mar 31;17(3):1605-1616. doi: 10.21037/jtd-24-1561. Epub 2025 Mar 26.
2
Network pharmacology predicts targets and pathways of herbal components for the treatment of pneumonia: A review.网络药理学预测治疗肺炎的草药成分的靶点和途径:综述
Medicine (Baltimore). 2025 Jan 31;104(5):e41372. doi: 10.1097/MD.0000000000041372.
3
Downregulation of ROR2 attenuates LPS-induced A549 cell injury through JNK and ERK signaling pathways.

本文引用的文献

1
Shema Oral Liquid Ameliorates the Severity of LPS-Induced COPD Regulating DNMT1.舍曲林口服液通过调节DNMT1改善脂多糖诱导的慢性阻塞性肺疾病的严重程度。
Front Pharmacol. 2022 Jun 8;13:903593. doi: 10.3389/fphar.2022.903593. eCollection 2022.
2
OLFM4 Regulates Lung Epithelial Cell Function in Sepsis-Associated ARDS/ALI via LDHA-Mediated NF-κB Signaling.OLFM4通过LDHA介导的NF-κB信号通路调节脓毒症相关急性呼吸窘迫综合征/急性肺损伤中的肺上皮细胞功能。
J Inflamm Res. 2021 Dec 18;14:7035-7051. doi: 10.2147/JIR.S335915. eCollection 2021.
3
[Study on mechanism of Qinbaohong Oral Liquid in anti-inflammation, stopping cough, eliminating phlegm and relieving asthma based on network pharmacology].
下调 ROR2 通过 JNK 和 ERK 信号通路减轻 LPS 诱导的 A549 细胞损伤。
Immun Inflamm Dis. 2023 Apr;11(4):e803. doi: 10.1002/iid3.803.
4
Combination of transcriptional biomarkers and clinical parameters for early prediction of sepsis indued acute respiratory distress syndrome.转录生物标志物与临床参数联合用于早期预测脓毒症诱导的急性呼吸窘迫综合征。
Front Immunol. 2023 Jan 4;13:1084568. doi: 10.3389/fimmu.2022.1084568. eCollection 2022.
基于网络药理学的芩暴红口服液抗炎、止咳、祛痰、平喘作用机制研究
Zhongguo Zhong Yao Za Zhi. 2021 Nov;46(22):5902-5911. doi: 10.19540/j.cnki.cjcmm.20210811.401.
4
Anti-inflammatory activity of lefamulin versus azithromycin and dexamethasone in vivo and in vitro in a lipopolysaccharide-induced lung neutrophilia mouse model.左福米林在脂多糖诱导的肺嗜中性粒细胞增多症小鼠模型中体内和体外与阿奇霉素和地塞米松的抗炎活性。
PLoS One. 2021 Sep 29;16(9):e0237659. doi: 10.1371/journal.pone.0237659. eCollection 2021.
5
BMSC-Derived Exosomes Ameliorate LPS-Induced Acute Lung Injury by miR-384-5p-Controlled Alveolar Macrophage Autophagy.骨髓间充质干细胞来源的外泌体通过 miR-384-5p 调控肺泡巨噬细胞自噬改善脂多糖诱导的急性肺损伤。
Oxid Med Cell Longev. 2021 Jun 13;2021:9973457. doi: 10.1155/2021/9973457. eCollection 2021.
6
Olfactomedin 4-Positive Neutrophils Are Upregulated after Hemorrhagic Shock.嗅鞘蛋白 4 阳性中性粒细胞在失血性休克后上调。
Am J Respir Cell Mol Biol. 2021 Feb;64(2):216-223. doi: 10.1165/rcmb.2020-0276OC.
7
Serum levels of olfactomedin 4: a biomarker for asthma control state in asthmatics.嗅觉介素4的血清水平:哮喘患者哮喘控制状态的生物标志物
Ann Transl Med. 2020 Apr;8(7):494. doi: 10.21037/atm.2020.03.213.
8
Two novel flavonoids from the leaves of L. with their inhibition of TNF-α production in LPS-induced RAW 264.7 cells.从 L. 的叶子中分离得到的两种新型黄酮类化合物及其对 LPS 诱导的 RAW 264.7 细胞中 TNF-α 产生的抑制作用。
Nat Prod Res. 2021 Apr;35(8):1331-1339. doi: 10.1080/14786419.2019.1648455. Epub 2019 Aug 6.
9
A new pentacyclic triterpenoid from the leaves of L. with inhibition of NO production in LPS-induced RAW 264.7 cells.从 L. 的叶子中分离得到的一种新的五环三萜,具有抑制 LPS 诱导的 RAW 264.7 细胞中 NO 产生的作用。
Nat Prod Res. 2020 Dec;34(23):3313-3319. doi: 10.1080/14786419.2019.1566822. Epub 2019 Feb 27.
10
Isolation of a new natural kingiside aglucone derivative and other anti-inflammatory constituents from .从 中分离得到一种新的天然 kingiside 苷元衍生物和其他抗炎成分。
Nat Prod Res. 2020 Feb;34(4):518-524. doi: 10.1080/14786419.2018.1490903. Epub 2018 Nov 23.