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1
The derivation of an inbred line of rats which develop asthma-like symptoms following challenge with aerosolized antigen.一种近交系大鼠的培育,该大鼠在接受雾化抗原激发后会出现类似哮喘的症状。
Immunology. 1981 Jan;42(1):19-24.
2
The respiratory response of sensitized rats to challenge with antigen aerosols.致敏大鼠对抗原气雾剂激发的呼吸反应。
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3
Suppression of the asthmatic phenotype by ultraviolet B-induced, antigen-specific regulatory cells.紫外线B诱导的抗原特异性调节细胞对哮喘表型的抑制作用
Clin Exp Allergy. 2007 Sep;37(9):1267-76. doi: 10.1111/j.1365-2222.2007.02750.x.
4
The respiratory response in sensitized rats to aerosol challenge.致敏大鼠对气雾剂激发的呼吸反应。
Immunology. 1978 Mar;34(3):465-70.
5
Changes in asthma-like responses after extended removal from exposure to trimellitic anhydride in the Brown Norway rat model.在棕色挪威大鼠模型中,长时间去除偏苯三酸酐暴露后哮喘样反应的变化。
Clin Exp Allergy. 2009 Nov;39(11):1746-53. doi: 10.1111/j.1365-2222.2009.03304.x. Epub 2009 Jun 22.
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Genome-wide profiling of antigen-induced time course expression using murine models for acute and chronic asthma.使用急性和慢性哮喘小鼠模型对抗原诱导的时间进程表达进行全基因组分析。
Int Arch Allergy Immunol. 2008;146(1):44-56. doi: 10.1159/000112502. Epub 2007 Dec 14.
7
Interference of methysergide, a specific 5-hydroxytryptamine receptor antagonist, with airway chronic allergic inflammation and remodelling in a murine model of asthma.甲基麦角新碱(一种特异性5-羟色胺受体拮抗剂)对哮喘小鼠模型气道慢性变应性炎症和重塑的干预作用
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Ovalbumin-sensitized mice are good models for airway hyperresponsiveness but not acute physiological responses to allergen inhalation.卵清蛋白致敏的小鼠是气道高反应性的良好模型,但不是吸入过敏原后急性生理反应的良好模型。
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Epigallocatechin-3-gallate reduces allergen-induced asthma-like reaction in sensitized guinea pigs.表没食子儿茶素-3-没食子酸酯可减轻致敏豚鼠中变应原诱导的哮喘样反应。
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IgE production, antigen-induced airway inflammation and airway hyperreactivity in the brown Norway rat: the effects of ricin.棕色挪威大鼠中IgE的产生、抗原诱导的气道炎症和气道高反应性:蓖麻毒素的影响。
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1
The tripeptide FEG ameliorates systemic inflammatory responses to rat intestinal anaphylaxis.三肽FEG可改善大鼠肠道过敏反应引起的全身炎症反应。
BMC Physiol. 2002 Aug 19;2:13. doi: 10.1186/1472-6793-2-13.
2
Different strains of rats develop different clinical forms of adjuvant disease.不同品系的大鼠会发展出不同临床形式的佐剂病。
Ann Rheum Dis. 1982 Oct;41(5):538-43. doi: 10.1136/ard.41.5.538.
3
Inhibition of allergen-induced bronchoconstriction in hyperreactive rats as a model for testing 5-lipoxygenase inhibitors and leukotriene D4 receptor antagonists.以高反应性大鼠变应原诱导的支气管收缩抑制作为测试5-脂氧合酶抑制剂和白三烯D4受体拮抗剂的模型。
Agents Actions. 1987 Oct;22(1-2):69-74. doi: 10.1007/BF01968819.
4
Animal models for testing anti-inflammatory drugs for treatment of bronchial hyperreactivity in asthma.用于测试抗炎药物治疗哮喘支气管高反应性的动物模型。
Pharm Weekbl Sci. 1991 Dec 13;13(6):225-37. doi: 10.1007/BF02015576.

本文引用的文献

1
Two lines of guinea pigs sensitive and nonsensitive to chemical mediators and anaphylaxis.对化学介质和过敏反应敏感和不敏感的两行豚鼠。
J Allergy. 1971 May;47(5):247-61. doi: 10.1016/s0091-6749(71)80003-9.
2
The inhibition by dexamethasone and disodium cromoglycate of anaphylactic bronchoconstriction in the rat.地塞米松和色甘酸钠对大鼠过敏性支气管收缩的抑制作用。
Br J Pharmacol. 1972 Sep;46(1):56-65. doi: 10.1111/j.1476-5381.1972.tb06848.x.
3
Active bronchial anaphylaxis in the rat.大鼠的主动性支气管过敏反应
Can J Physiol Pharmacol. 1974 Dec;52(6):1114-8. doi: 10.1139/y74-146.
4
Animal models of the asthmatic state.哮喘状态的动物模型。
Annu Rev Med. 1974;25(0):53-68. doi: 10.1146/annurev.me.25.020174.000413.
5
Effect of disodium cromoglycate on various types of anaphylactic reaction in the guinea pig.色甘酸钠对豚鼠各类过敏反应的影响。
Int Arch Allergy Appl Immunol. 1973;45(6):795-807. doi: 10.1159/000231080.
6
Immunochemical and biologic properties of rat IgE. I. Immunochemical identification of rat IgE.大鼠IgE的免疫化学和生物学特性。I. 大鼠IgE的免疫化学鉴定。
J Immunol. 1970 Nov;105(5):1082-6.
7
Effect of prostaglandins F2 alpha and E2 on airway conductance in healthy subjects and asthmatic patients.前列腺素F2α和E2对健康受试者及哮喘患者气道传导率的影响。
Am Rev Respir Dis. 1975 Mar;111(3):313-20. doi: 10.1164/arrd.1975.111.3.313.
8
IgE-mediated anaphylactic bronchoconstriction in the guinea pig and the effect of disodium cromoglycate.豚鼠中IgE介导的过敏性支气管收缩及色甘酸钠的作用。
Int Arch Allergy Appl Immunol. 1976;50(3):322-8. doi: 10.1159/000231509.
9
Mediators of passive lung anaphylaxis in the rat.大鼠被动性肺过敏反应的介质
Br J Pharmacol. 1975 Sep;55(1):57-64. doi: 10.1111/j.1476-5381.1975.tb07610.x.
10
Site of respiratory reaction in allergic rats challenged via the airways.经气道激发的变应性大鼠的呼吸反应部位
Int Arch Allergy Appl Immunol. 1978;57(4):358-63. doi: 10.1159/000232125.

一种近交系大鼠的培育,该大鼠在接受雾化抗原激发后会出现类似哮喘的症状。

The derivation of an inbred line of rats which develop asthma-like symptoms following challenge with aerosolized antigen.

作者信息

Holme G, Piechuta H

出版信息

Immunology. 1981 Jan;42(1):19-24.

PMID:7461723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1458206/
Abstract

Sensitized Sprague-Dawley rats developed respiratory impairment after challenge with aerosolized antigen. The response to challenge was heterogeneous. A proportion of each group of rats developed dyspnea and other symptoms similar to asthma; the remainder developed apnea but no other symptoms. Selective breeding from rats which developed dyspnea increased the incidence from 44% in F0 to 55% in F1 and greater than 90% in F2 and F3. Inbreeding also produced a significant increase in the duration of antigen-induced dyspnea. The results from the selective inbreeding suggest antigen-induced dyspnea is controlled genetically, possibly by multiple gene loci. These inbred rats constitute a population which have a predictable response to aerosolized antigen challenge. They should have utility in investigating allergic asthma and evaluating potential new drugs.

摘要

致敏的斯普拉格-道利大鼠在接受雾化抗原激发后出现呼吸功能损害。对激发的反应具有异质性。每组大鼠中有一部分出现呼吸困难和其他类似哮喘的症状;其余的则出现呼吸暂停但无其他症状。从出现呼吸困难的大鼠中进行选择性育种,使发病率从F0代的44%增加到F1代的55%,在F2代和F3代中超过90%。近亲繁殖也使抗原诱导的呼吸困难持续时间显著增加。选择性近亲繁殖的结果表明,抗原诱导的呼吸困难受遗传控制,可能由多个基因位点控制。这些近交系大鼠构成了一个对雾化抗原激发有可预测反应的群体。它们在研究过敏性哮喘和评估潜在新药方面应具有实用价值。