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吸入雷公藤内酯醇对哮喘小鼠气道炎症的影响。

The Effects of Nebulized Inhaled Triptolide on Airway Inflammation in a Mouse Model of Asthma.

机构信息

PCCM, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201318, China.

出版信息

Can Respir J. 2023 Aug 21;2023:2983092. doi: 10.1155/2023/2983092. eCollection 2023.

DOI:10.1155/2023/2983092
PMID:37645252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10462443/
Abstract

Inhalation of nebulized TP has received little attention in the past. Here, we intend to investigate the effect of nebulized inhaled TP on airway inflammation in a mouse model of asthma. 29 SPF BALB/c mice were divided into four groups: blank control (Blk,  = 5), normal saline (NS,  = 8), dexamethasone (Dex,  = 8), and TP ( = 8). During the process of sensitization, mice in the three intervention groups were treated with nebulized NS, an injection of Dex, and nebulized triptolide, respectively. Then bronchoalveolar lavage fluid (BALF), peripheral blood, and lung tissue were collected. Relevant cytokines, transcriptional factors, and CD4+Th17+ T cell proportions were assessed and compared. IL-6, IL-17, IL-23, and TGF-1 demonstrated a significant difference between groups in the following order: Dex < TP < NS ( ≤ 0.001), while IL-10 changed in the opposite direction ( < 0.001). At the transcriptional level in lung tissue, the Ct value of IL-17 in the Dex group was significantly higher than in the NS and TP groups ( < 0.001). Meanwhile, it was higher in the TP group than in the NS group ( < 0.001). The Ct value of RORt demonstrated a significant difference among three groups in the following order: Dex > TP > NS ( < 0.001). An opposite trend of FoxP3 Ct value was revealed in the order: NS > TP > Dex. The proportion of CD4+Th17+ cells was 9.53 ± 2.74% in the NS group, 4.23 ± 2.26% in the Dex group, and 6.76 ± 2.99% in the TP group, which shows significant differences between the NS and Dex ( < 0.001) or NS and TP groups ( < 0.05). Inhalation of nebulized triptolide can play a role in suppressing airway inflammation with inflammatory cytokines and transcriptional factors reduced and CD4+Th17+ T cells dampened, also in a manner less than injected dexamethasone.

摘要

雾化吸入雷公藤红素(Triptolide,TP)在过去受到的关注较少。本研究旨在探讨雾化吸入 TP 对哮喘小鼠模型气道炎症的影响。29 只 SPF BALB/c 小鼠分为 4 组:空白对照组(Blk,n=5)、生理盐水组(NS,n=8)、地塞米松组(Dex,n=8)和 TP 组(n=8)。在致敏过程中,3 个干预组分别用雾化 NS、地塞米松注射和雾化雷公藤红素处理。然后收集支气管肺泡灌洗液(BALF)、外周血和肺组织。评估并比较相关细胞因子、转录因子和 CD4+Th17+T 细胞比例。IL-6、IL-17、IL-23 和 TGF-β1 组间差异有统计学意义,按 Dex<TP<NS(≤0.001)的顺序排列,而 IL-10 则呈相反方向变化(<0.001)。在肺组织的转录水平上,Dex 组 IL-17 的 Ct 值明显高于 NS 和 TP 组(<0.001),TP 组又高于 NS 组(<0.001)。RORt 的 Ct 值在 3 组间差异有统计学意义,按 Dex>TP>NS(<0.001)的顺序排列。FoxP3 Ct 值呈相反趋势,按 NS>TP>Dex 的顺序排列。NS 组 CD4+Th17+细胞比例为 9.53%±2.74%,Dex 组为 4.23%±2.26%,TP 组为 6.76%±2.99%,NS 组与 Dex 组(<0.001)或 NS 组与 TP 组(<0.05)比较差异有统计学意义。雾化吸入雷公藤红素可通过降低炎症细胞因子和转录因子,减少 CD4+Th17+T 细胞,发挥抑制气道炎症的作用,且作用弱于注射用地塞米松。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/9b0f176d75eb/CRJ2023-2983092.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/478a1322a964/CRJ2023-2983092.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/c7188bc0f9cc/CRJ2023-2983092.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/f70da33d8ca1/CRJ2023-2983092.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/74a3b5ef0ab2/CRJ2023-2983092.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/392623925a56/CRJ2023-2983092.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/9b0f176d75eb/CRJ2023-2983092.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/478a1322a964/CRJ2023-2983092.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/c7188bc0f9cc/CRJ2023-2983092.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/f70da33d8ca1/CRJ2023-2983092.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/74a3b5ef0ab2/CRJ2023-2983092.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/392623925a56/CRJ2023-2983092.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10462443/9b0f176d75eb/CRJ2023-2983092.006.jpg

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本文引用的文献

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Int J Mol Sci. 2023 Mar 2;24(5):4865. doi: 10.3390/ijms24054865.
2
Immunobiology of Steroid-Unresponsive Severe Asthma.类固醇无反应性重度哮喘的免疫生物学
Front Allergy. 2021 Aug 27;2:718267. doi: 10.3389/falgy.2021.718267. eCollection 2021.
3
Identification of key genes and pathways between mild-moderate and severe asthmatics via bioinformatics analysis.通过生物信息学分析鉴定轻中度和重度哮喘患者之间的关键基因和通路。
Sci Rep. 2022 Feb 15;12(1):2549. doi: 10.1038/s41598-022-06675-w.
4
Serum Amyloid A1: A Biomarker for Neutrophilic Airway Inflammation in Adult Asthmatic Patients.血清淀粉样蛋白A1:成人哮喘患者中性粒细胞气道炎症的生物标志物
Allergy Asthma Immunol Res. 2022 Jan;14(1):40-58. doi: 10.4168/aair.2022.14.1.40.
5
Application and Mechanisms of Triptolide in the Treatment of Inflammatory Diseases-A Review.雷公藤甲素在炎症性疾病治疗中的应用及机制——综述
Front Pharmacol. 2019 Dec 6;10:1469. doi: 10.3389/fphar.2019.01469. eCollection 2019.
6
Resolution of allergic asthma.过敏性哮喘的缓解。
Semin Immunopathol. 2019 Nov;41(6):665-674. doi: 10.1007/s00281-019-00770-3. Epub 2019 Nov 8.
7
Cellular mechanisms underlying steroid-resistant asthma.类固醇抵抗性哮喘的细胞机制。
Eur Respir Rev. 2019 Oct 21;28(153). doi: 10.1183/16000617.0096-2019. Print 2019 Sep 30.
8
A Novel Insight on Endotyping Heterogeneous Severe Asthma Based on Endoplasmic Reticulum Stress: Beyond the "Type 2/Non-Type 2 Dichotomy".基于内质网应激的异质性重症哮喘表型新见解:超越“2 型/非 2 型二分法”。
Int J Mol Sci. 2019 Feb 7;20(3):713. doi: 10.3390/ijms20030713.
9
Non-type 2 inflammation in severe asthma is propelled by neutrophil cytoplasts and maintained by defective resolution.中性粒细胞胞质体驱动严重哮喘中的非 2 型炎症,并通过缺陷性解决来维持。
Allergol Int. 2019 Apr;68(2):143-149. doi: 10.1016/j.alit.2018.11.006. Epub 2018 Dec 17.
10
Neutrophil cytoplasts induce T17 differentiation and skew inflammation toward neutrophilia in severe asthma.中性粒细胞胞质体制剂可诱导 T17 分化,并使严重哮喘中的炎症向中性粒细胞增多倾斜。
Sci Immunol. 2018 Aug 3;3(26). doi: 10.1126/sciimmunol.aao4747.