Evaluation of Artemisia annua-Scutellaria baicalensis Herb Pair Carbon Dots Interfering NLRP3 Inflammatory Pathway For Effective Against H1N1 Viral Pneumonia in Mice Model

黄芩 病毒性肺炎 促炎细胞因子 免疫学 甲型流感病毒 炎症体 免疫系统 生物 鼻腔给药 青蒿 免疫 先天免疫系统 医学 炎症 中医药 转录组 肺炎 肺 免疫印迹 病毒 细胞因子 外体 信号转导 发病机制 实时聚合酶链反应 布鲁氏菌 污渍 肺泡巨噬细胞 吲哚胺2,3-双加氧酶 药理学 基因沉默 A549电池 病毒学 半胱氨酸蛋白酶1 细胞凋亡 CD11c公司
作者
Qianyun Zhang,Xinyi Huang,Huimei Kong,Qiongyao Liang,Xiaoqing Lv,Yuan Ma,Jingbo Wang,Jing Chen
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 21: 1-17 被引量:1
标识
DOI:10.2147/ijn.s566658
摘要

Purpose: Influenza is an acute respiratory infectious disease with high transmissibility and significant pandemic potential worldwide. In recent years, traditional Chinese medicine (TCM)-based carbon dots (CDs) have emerged as promising therapeutic agents owing to their favorable biosafety profile and potent anti-inflammatory and immunomodulatory properties. The present study aimed to investigate the therapeutic effects of TCM-derived CDs on influenza A virus (IAV)-induced pneumonia, and elucidate their underlying molecular mechanisms of action. Mouse Model and Methods: A murine model of IAV-induced pneumonia was established via intranasal instillation and subsequently treated with CDs co-derived from Artemisia annua and Scutellaria baicalensis (QH-CDs). Results: The results demonstrated that, compared to the observations in the model group, treatment with QH-CDs significantly alleviated the pathological damages to lung tissue, reduced the lung index, and promoted body weight recovery. QH-CDs treatment reduced the expression of key inflammatory cytokines (IL-1β, IL-6) in lung tissue by over 60% compared to the model group (p < 0.0001). In addition, QH-CDs reduce lung viral titers by more than 70%, indicating that they have combined antiviral and anti-inflammatory effects. Transcriptomic analysis revealed that treatment with QH-CDs reversed the alterations in the expression patterns of several genes associated with immunity and inflammation. The differentially expressed genes were predominantly involved in immune regulation, cytokine activity, and inflammatory signaling pathways. The results of Quantitative Real-time polymerase chain reaction (qPCR) show that the mRNA expression levels of NLRP3, Caspase-1, and IL-1β all significantly decreased. Protein expression analyses by Western blotting further confirmed the critical role of the NLRP3 inflammasome signaling pathway in mediating the therapeutic effects of QH-CDs. Conclusion: QH-CDs therapeutic effects may be closely related to the regulation of immune responses, inhibition of inflammatory responses, and modulation of the NLRP3 signaling pathway. This study provides novel insights into the therapeutic application of TCM-derived nanomaterials for the treatment of viral pneumonia.
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