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使用气压体积描记法对过敏性小鼠气道反应性进行无创测量。

Noninvasive measurement of airway responsiveness in allergic mice using barometric plethysmography.

作者信息

Hamelmann E, Schwarze J, Takeda K, Oshiba A, Larsen G L, Irvin C G, Gelfand E W

机构信息

Department of Pediatrics, National Jewish Medical and Research Center, Denver, Colorado, USA.

出版信息

Am J Respir Crit Care Med. 1997 Sep;156(3 Pt 1):766-75. doi: 10.1164/ajrccm.156.3.9606031.

DOI:10.1164/ajrccm.156.3.9606031
PMID:9309991
Abstract

To study the mechanisms and kinetics underlying the development of increased airway responsiveness (AR) after allergic sensitization, animal models have been invaluable. Using barometric whole-body plethysmography and increases in enhanced pause (Penh) as an index of airway obstruction, we measured responses to inhaled methacholine in conscious, unrestrained mice after sensitization and airway challenge with ovalbumin (OVA). Sensitized and challenged animals had significantly increased AR to aerosolized methacholine compared with control animals. AR measured as Penh was associated with increased IgE production and eosinophil lung infiltration. In a separate approach we confirmed the involvement of the lower airways in the response to aerosolized methacholine using tracheotomized mice. Increases in Penh values after methacholine challenge were also correlated with increased intrapleural pressure, measured via an esophageal tube. Lastly, mice demonstrating AR using a noninvasive technique also demonstrated increased pulmonary resistance responses to aerosolized methacholine when measured using an invasive technique the following day in the same animals. The increases in Penh values were inhibited by pretreatment of the mice with a beta 2-agonist. These data indicate that measurement of AR to inhaled methacholine by barometric whole-body plethysmography is a valid indicator of airway hyperresponsiveness after allergic sensitization in mice. The measurement of AR in unrestrained, conscious animals provides new opportunities to evaluate the mechanisms and kinetics underlying the development and maintenance of airway hyperresponsiveness and to assess various therapeutic interventions.

摘要

为了研究变应原致敏后气道反应性(AR)增加的潜在机制和动力学,动物模型具有重要价值。使用气压式全身体积描记法并以增强暂停(Penh)增加作为气道阻塞指标,我们在卵清蛋白(OVA)致敏和气道激发后,测量了清醒、未束缚小鼠对吸入乙酰甲胆碱的反应。与对照动物相比,致敏和激发的动物对雾化乙酰甲胆碱的AR显著增加。以Penh测量的AR与IgE产生增加和嗜酸性粒细胞肺浸润有关。在另一种方法中,我们使用气管切开的小鼠证实了下呼吸道参与了对雾化乙酰甲胆碱的反应。乙酰甲胆碱激发后Penh值的增加也与通过食管插管测量的胸膜腔内压增加相关。最后,使用无创技术显示有AR的小鼠,在第二天对同一只动物使用有创技术测量时,对雾化乙酰甲胆碱的肺阻力反应也增加。用β2-激动剂预处理小鼠可抑制Penh值的增加。这些数据表明,通过气压式全身体积描记法测量对吸入乙酰甲胆碱的AR是小鼠变应原致敏后气道高反应性的有效指标。在未束缚的清醒动物中测量AR为评估气道高反应性发生和维持的潜在机制和动力学以及评估各种治疗干预措施提供了新机会。

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