The impact of estrogen replacement during perimenopause on lung function and airway inflammation in the VCD mouse model.

IF 3.8 2区 医学 Q1 PHYSIOLOGY
William P Pederson, Laurie Michelle Ellerman, Riley D Hellinger, Joselyn Joanna Rojas Quintero, Francesca Polverino, John P Konhilas, Julie G Ledford
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引用次数: 0

Abstract

Menopause associated asthma impacts a subset of women and is less responsive to current treatments. Mechanisms driving this late-onset asthma are unknown. We recently developed a mouse model of menopause associated asthma using a combination of 4-vinylcyclohexene diepoxide (VCD) and house dust mite (HDM) exposures. The goal of this study was to determine how hormone replacement therapy during perimenopause impacts lung function and inflammation. The experimental groups included menopausal mice (VCD) with and without exposure to HDM (to model allergic airways disease) and menopausal mice with and without hormone replacement therapy (HRT; via estrogen pellet implantation). Lung function during methacholine challenge was assessed by flexiVent. Serum, bronchoalveolar lavage fluid (BALF), and histological samples were collected for assessment. Mice that received HRT during perimenopause had enhanced airway hyperresponsiveness (AHR) detected by total airway resistance (Rrs), tissue damping (G), and downward shifts in pressure-volume (PV) curves compared with controls, independent of HDM challenge. Although HRT in perimenopause resulted in decreased eosinophils in the HDM model, neutrophil levels and mucus production were unchanged. Mice receiving HRT in perimenopause also had significantly increased collagen production and inflammation associated with large and small airways, independent of HDM challenge. HRT given during perimenopause may be detrimental to lung responses, including increased AHR and decreased lung function, as well as increased tissue inflammation and airway remodeling.NEW & NOTEWORTHY Menopause-associated asthma is a subtype of asthma that is still largely unexplored and difficult to manage. Women experiencing menopause-associated asthma often have more severe exacerbations, higher rates of exacerbation, and most importantly, poor response to standard treatments. This study examined the impact of estrogen replacement given during the perimenopause phase on lung inflammation and function after menopause. While decreasing eosinophil recruitment, estrogen replacement actually led to worse lung function and more airway remodeling.

围绝经期雌激素替代对VCD小鼠肺功能和气道炎症的影响。
背景:绝经期相关哮喘影响一小部分妇女,对目前的治疗反应较差。导致这种晚发性哮喘的机制尚不清楚。我们最近建立了绝经期哮喘小鼠模型,使用4-乙烯基环己烯二氧化物(VCD)和室内尘螨(HDM)暴露的组合。本研究的目的是确定围绝经期激素替代疗法如何影响肺功能和炎症。方法:实验组包括有和没有暴露于HDM(模拟过敏性气道疾病)的绝经期小鼠(VCD)和有和没有激素替代治疗(HRT;通过雌激素颗粒植入)的绝经期小鼠。使用Flexivent评估甲胆碱刺激时的肺功能。收集血清、BALF和组织学样本进行评估。结果:与对照组相比,经总气道阻力(Rrs)、组织阻尼(G)和pv曲线向下移动检测,围绝经期接受HRT的小鼠气道高反应性(AHR)增强,与HDM无关。虽然围绝经期HRT导致HDM模型中嗜酸性粒细胞减少,但中性粒细胞水平和粘液生成不变。在围绝经期接受HRT的小鼠也显著增加了胶原蛋白的产生和与大气道和小气道相关的炎症,与HDM无关。结论:围绝经期给予HRT可能对肺反应有害,包括AHR增加和肺功能下降,以及组织炎症和气道重塑增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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