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免疫后卵清蛋白激发试验可引起豚鼠嗜酸性粒细胞募集,但不会导致支气管高反应性:时间进程及其与嗜酸性粒细胞活化状态的关系

Ovalbumin challenge following immunization elicits recruitment of eosinophils but not bronchial hyperresponsiveness in guinea-pigs: time course and relationship to eosinophil activation status.

作者信息

Banner K H, Paul W, Page C P

机构信息

Department of Pharmacology, King's College London, UK.

出版信息

Pulm Pharmacol. 1996 Jun;9(3):179-87. doi: 10.1006/pulp.1996.0021.

Abstract

Eosinophils are known to be present in the airways of allergic asthmatics, and have been suggested to contribute to the pathophysiological changes accompanying this condition, particularly hyperresponsiveness to airway spasmogens. However, a causal relationship between pulmonary eosinophil accumulation and bronchial hyperresponsiveness in asthma is not proven. In the present study, the time course of pulmonary cell influx was investigated in an immunized guinea-pig model. Eosinophil activation status was also determined together with the bronchial responsiveness to histamine. Guinea-pigs were sensitized [20 micrograms ovalbumin (OVA) per animal in A1(OH)3 (0.5 ml) i.p.] and subsequently challenged with aerosolized OVA (100 micrograms/ml) for 1 h 18-21 days later. At different time points (1 h to 72 h) after OVA challenge, bronchial responses to i.v. histamine were measured and bronchoalveolar lavage (BAL) was performed to assess pulmonary cell influx. Eosinophil peroxidase (EPO) and total protein levels were measured in BAL fluid supernatants. Exposure of sensitized animals to aerosolized OVA produced a significant increase (P < 0.05 vs. sham immunized) in eosinophil infiltration 24 h later which was sustained up to 72 h. Despite this, OVA challenge did not cause either eosinophil activation, as measured by EPO release, or bronchial hyperresponsiveness to histamine at any of the time points examined. These data show that allergen challenge of sensitized guinea-pigs can elicit airway eosinophil accumulation without accompanying airways hyperresponsiveness or eosinophil activation.

摘要

已知嗜酸性粒细胞存在于过敏性哮喘患者的气道中,并被认为会导致伴随这种疾病的病理生理变化,尤其是对气道痉挛原的高反应性。然而,哮喘患者肺部嗜酸性粒细胞积聚与支气管高反应性之间的因果关系尚未得到证实。在本研究中,我们在免疫豚鼠模型中研究了肺细胞流入的时间进程。同时还测定了嗜酸性粒细胞的激活状态以及支气管对组胺的反应性。将豚鼠致敏[每只动物腹腔注射20微克卵清蛋白(OVA)于0.5毫升氢氧化铝(A1(OH)3)中],并在18 - 21天后用雾化的OVA(100微克/毫升)激发1小时。在OVA激发后的不同时间点(1小时至72小时),测量静脉注射组胺后的支气管反应,并进行支气管肺泡灌洗(BAL)以评估肺细胞流入情况。测定BAL液上清液中的嗜酸性粒细胞过氧化物酶(EPO)和总蛋白水平。致敏动物暴露于雾化OVA后24小时,嗜酸性粒细胞浸润显著增加(与假免疫组相比,P < 0.05),并持续至72小时。尽管如此,在任何检测时间点上,OVA激发均未导致通过EPO释放测定的嗜酸性粒细胞激活,也未引起支气管对组胺的高反应性。这些数据表明,致敏豚鼠的过敏原激发可引发气道嗜酸性粒细胞积聚,而不伴有气道高反应性或嗜酸性粒细胞激活。

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