In mouse model of mixed granulocytic asthma with corticosteroid refractoriness, Bronchom mitigates airway hyperresponsiveness, inflammation and airway remodeling.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2024-08-11 DOI:10.1186/s10020-024-00888-7
Acharya Balkrishna, Sandeep Sinha, Anupam Pandey, Surjeet Singh, Monali Joshi, Rani Singh, Anurag Varshney
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Abstract

Background: Asthma is a heterogeneous, inflammatory disease with several phenotypes and endotypes. Severe asthmatics often exhibit mixed granulocytosis with reduced corticosteroid sensitivity. Bronchom is a newly developed Ayurvedic prescription medicine, indicated for the treatment of obstructive airway disorders. The purpose of the present study was to evaluate the in-vivo efficacy of Bronchom in mouse model of mixed granulocytic asthma with steroidal recalcitrance.

Methods: High-performance thin layer chromatography (HPTLC) and Ultra-high performance liquid chromatography (UHPLC) were employed to identify and quantitate the phytometabolites present in Bronchom. The preclinical effectiveness of Bronchom was assessed in house dust mite (HDM) and Complete Freund's adjuvant (CFA)-induced mixed granulocytic asthma model in mice. High dose of dexamethasone was tested parallelly. Specific-pathogen-free C57BL/6 mice were immunized with HDM and CFA and nineteen days later, they were intranasally challenged with HDM for four consecutive days. Then the mice were challenged with nebulized methacholine to evaluate airway hyperresponsiveness (AHR). Inflammatory cell influx was enumerated in the bronchoalveolar lavage fluid (BALF) followed by lung histology. Additionally, the concentrations of Th2 and pro-inflammatory cytokines was assessed in the BALF by multiplexed immune assay. The mRNA expression of pro-inflammatory cytokines and Mucin 5AC (MUC5AC) was also evaluated in the lung.

Results: HPTLC fingerprinting and UHPLC quantification of Bronchom revealed the presence of bioactive phytometabolites, namely, rosmarinic acid, gallic acid, methyl gallate, piperine, eugenol and glycyrrhizin. Bronchom effectively reduced AHR driven by HDM-CFA and the influx of total leukocytes, eosinophils and neutrophils in the BALF. In addition, Bronchom inhibited the infiltration of inflammatory cells in the lung as well as goblet cell metaplasia. Further, it also suppressed the elevated levels of Th2 cytokines and pro-inflammatory cytokines in the BALF. Similarly, Bronchom also regulated the mRNA expression of pro-inflammatory cytokines as well as MUC5AC in mice lungs. Reduced effectiveness of a high dose of the steroid, dexamethasone was observed in the model.

Conclusions: We have demonstrated for the first time the robust pharmacological effects of an herbo-mineral medicine in an animal model of mixed granulocytic asthma induced by HDM and CFA. The outcomes suggest the potential utility of Bronchom in severe asthmatics with a mixed granulocytic phenotype.

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在皮质类固醇难治性混合粒细胞哮喘小鼠模型中,Bronchom 可减轻气道高反应性、炎症和气道重塑。
背景:哮喘是一种异质性炎症性疾病,有多种表型和内型。严重的哮喘患者通常表现为混合性粒细胞增多症,对皮质类固醇的敏感性降低。Bronchom 是一种新开发的阿育吠陀处方药,适用于治疗阻塞性气道疾病。本研究的目的是评估 Bronchom 在小鼠混合性粒细胞性哮喘模型中的体内疗效。方法:采用高效薄层色谱法(HPTLC)和超高效液相色谱法(UHPLC)对 Bronchom 中的植物代谢物进行鉴定和定量。在屋尘螨(HDM)和完全弗氏佐剂(CFA)诱导的小鼠混合粒细胞哮喘模型中,对 Bronchom 的临床前有效性进行了评估。同时还测试了大剂量地塞米松。用HDM和CFA免疫无特异性病原体的C57BL/6小鼠,19天后用HDM对小鼠进行连续四天的鼻内挑战。然后用雾化甲基胆碱对小鼠进行挑战,以评估气道高反应性(AHR)。对支气管肺泡灌洗液(BALF)中的炎性细胞流入量进行计数,然后进行肺组织学检查。此外,还通过多重免疫测定评估了支气管肺泡灌洗液中 Th2 和促炎细胞因子的浓度。还评估了肺部促炎细胞因子和粘蛋白 5AC (MUC5AC) 的 mRNA 表达:结果:HPTLC指纹图谱和超高效液相色谱定量分析显示,Bronchom含有生物活性植物代谢物,即迷迭香酸、没食子酸、没食子酸甲酯、胡椒碱、丁香酚和甘草苷。Bronchom能有效降低HDM-CFA引起的AHR,减少BALF中白细胞总数、嗜酸性粒细胞和中性粒细胞的流入。此外,Bronchom 还能抑制肺部炎症细胞的浸润以及上皮细胞的增生。此外,它还抑制了 BALF 中 Th2 细胞因子和促炎细胞因子水平的升高。同样,Bronchom 还能调节小鼠肺部促炎细胞因子和 MUC5AC 的 mRNA 表达。在该模型中观察到高剂量类固醇地塞米松的效果降低:我们首次在由 HDM 和 CFA 诱导的混合性粒细胞哮喘动物模型中证明了草本矿物质药物的强大药理作用。结果表明,Bronchom 对具有混合粒细胞表型的严重哮喘患者具有潜在的实用性。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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