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本文引用的文献

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Bronchial mucosal permeability and its relationship to airways hyperreactivity.支气管黏膜通透性及其与气道高反应性的关系。
J Allergy Clin Immunol. 1981 Jun;67(6):421-5. doi: 10.1016/0091-6749(81)90094-4.
2
Airway responses to sequential challenges with platelet-activating factor and leukotriene D4 in rhesus monkeys.恒河猴气道对血小板活化因子和白三烯D4序贯激发的反应
J Lab Clin Med. 1984 Sep;104(3):340-5.
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Biology and biochemistry of platelet-activating factor.血小板活化因子的生物学与生物化学
Clin Rev Allergy. 1983 Sep;1(3):353-67. doi: 10.1007/BF02991226.
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Mediator release after nasal airway challenge with allergen.变应原进行鼻气道激发后介质的释放。
Am Rev Respir Dis. 1983 Oct;128(4):597-602. doi: 10.1164/arrd.1983.128.4.597.
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Vitamin E protection of membrane lipids during electron transport functions.电子传递功能期间维生素E对膜脂的保护作用。
Ann N Y Acad Sci. 1972 Dec 18;203:62-73. doi: 10.1111/j.1749-6632.1972.tb27858.x.
6
Sequence of pathologic changes in the airway mucosa of guinea pigs during ozone-induced bronchial hyperreactivity.臭氧诱导豚鼠支气管高反应性过程中气道黏膜的病理变化序列
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7
The eosinophil and the pathophysiology of asthma.嗜酸性粒细胞与哮喘的病理生理学
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Nasal provocation with bradykinin induces symptoms of rhinitis and a sore throat.
Am Rev Respir Dis. 1988 Mar;137(3):613-6. doi: 10.1164/ajrccm/137.3.613.
9
Allergen-induced nasal hyperreactivity appears unrelated to the size of the nasal and dermal immediate allergic reaction.
Allergy. 1987 Nov;42(8):631-7. doi: 10.1111/j.1398-9995.1987.tb00395.x.
10
The effect of platelet activating factor on nasal hypersensitivity.
Eur J Clin Pharmacol. 1988;35(3):231-5. doi: 10.1007/BF00558258.

血小板活化因子对人鼻气道反应性的影响。

The effect of platelet-activating factor on the responsiveness of the human nasal airway.

作者信息

Austin C E, Foreman J C

机构信息

Department of Pharmacology, University College London.

出版信息

Br J Pharmacol. 1993 Sep;110(1):113-8. doi: 10.1111/j.1476-5381.1993.tb13779.x.

DOI:10.1111/j.1476-5381.1993.tb13779.x
PMID:8220870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2176011/
Abstract
  1. The effects of inhaled platelet-activating factor (PAF) on responsiveness of the human nasal airway were examined in normal subjects by measuring nasal airway resistance in response to histamine and bradykinin at 2, 6, 24, 48 h and 7 d after PAF administration. Eosinophil cationic protein (ECP) in nasal secretions was also measured. 2. Intranasal aerosol administration of PAF, 30 or 60 micrograms per nostril to normal human subjects induced an increased responsiveness to inhaled histamine, 50 to 400 micrograms and bradykinin, 100 micrograms per nostril at 2, 6 and 24 h following PAF treatment. However the effect was not apparent at 48 h or 7 days after PAF administration. 3. Intranasal administration of lyso-PAF, 60 micrograms by aerosol did not increase the reactivity of the nasal airway in response to histamine, 200 micrograms. 4. There was no difference in the time course of the PAF-induced hyperresponsiveness to histamine or bradykinin. 5. PAF-induced nasal hyperresponsiveness at 2 and 6 h was associated with increases in the ECP concentration of the nasal lavage fluid. 6. Vitamin E pretreatment of subjects resulted in the attenuation of the PAF-induced hyperresponsiveness to histamine, and a decrease in ECP levels of the nasal lavage fluid. 7. The results suggest that in the human nasal airway, PAF induces a non-specific hyperresponsiveness which is accompanied by eosinophil activation in the nasal cavity. Free radical production induced by PAF may contribute to the hyperresponsiveness and the activation of eosinophils.
摘要
  1. 通过在给予血小板活化因子(PAF)后2、6、24、48小时及7天测量正常受试者对组胺和缓激肽的鼻腔气道反应性,研究吸入PAF对人鼻腔气道反应性的影响。还测量了鼻分泌物中的嗜酸性粒细胞阳离子蛋白(ECP)。2. 向正常人体受试者每侧鼻腔内喷雾给予30或60微克PAF,在PAF治疗后2、6和24小时,可诱导对吸入组胺(每侧鼻腔50至400微克)和缓激肽(每侧鼻腔100微克)的反应性增加。然而,在给予PAF后48小时或7天时,这种作用并不明显。3. 经喷雾向鼻腔内给予60微克溶血PAF,并未增加鼻腔气道对200微克组胺的反应性。4. PAF诱导的对组胺或缓激肽的高反应性的时间进程没有差异。5. PAF在2和6小时诱导的鼻腔高反应性与鼻腔灌洗液中ECP浓度的增加有关。6. 对受试者进行维生素E预处理可减弱PAF诱导的对组胺的高反应性,并降低鼻腔灌洗液中的ECP水平。7. 结果表明,在人鼻腔气道中,PAF诱导一种非特异性高反应性,伴有鼻腔内嗜酸性粒细胞活化。PAF诱导的自由基产生可能促成高反应性和嗜酸性粒细胞的活化。