• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

致敏大鼠过敏原激发后早期和晚期气道反应期间胆汁中的白三烯

Leukotrienes in bile during the early and the late airway responses after allergen challenge of sensitized rats.

作者信息

Martin J G, Xu L J, Toh M Y, Olivenstein R, Powell W S

机构信息

Meakins-Christie Laboratories, McGill University, Montreal, Quebec, Canada.

出版信息

Am Rev Respir Dis. 1993 Jan;147(1):104-10. doi: 10.1164/ajrccm/147.1.104.

DOI:10.1164/ajrccm/147.1.104
PMID:8420402
Abstract

The Brown Norway rat produces high levels of IgE in response to active immunization and develops both early and late airway constrictor responses after subsequent allergen challenge. We have used this model of allergic asthma to investigate the temporal relationship between the in vivo synthesis of peptidoleukotrienes (peptido-LTs) and the late response. Brown Norway rats that had been sensitized by injection of ovalbumin 2 to 3 wk prior to the commencement of the experiment were subjected to bile duct cannulation and tracheal intubation. The rats were challenged 2 h later by intratracheal instillation of ovalbumin. Lung resistance was measured before and at frequent intervals after antigen challenge. Biliary peptido-LTs (LTC4, LTD4, LTE4, and N-acetyl-LTE4) were measured by a combination of high pressure liquid chromatography and radioimmunoassay in bile samples collected for a period of 1 h before instillation of ovalbumin, and between zero and 1 h, 1 and 4 h, 4 and 6 h, and 6 and 8 h, subsequently. All of the 10 rats subjected to antigen challenge developed early responses. Of these, six also developed late responses, whereas two died about 1 h after challenge. The levels of peptido-LTs excreted in bile between 4 and 8 h after antigen challenge (corresponding in time to the late responses) were about four times higher in the ovalbumin-instilled rats that developed late responses (n = 6) than in the ovalbumin-sensitized control rats that had been subjected to instillation of saline (n = 6; p < 0.02).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

经主动免疫后,棕色挪威大鼠会产生高水平的IgE,并在随后的过敏原激发后出现早期和晚期气道收缩反应。我们利用这种过敏性哮喘模型来研究肽白三烯(peptido-LTs)的体内合成与迟发反应之间的时间关系。在实验开始前2至3周通过注射卵清蛋白致敏的棕色挪威大鼠,接受胆管插管和气管插管。2小时后,通过气管内滴注卵清蛋白对大鼠进行激发。在抗原激发前及激发后频繁测量肺阻力。在滴注卵清蛋白前1小时收集胆汁样本,随后在0至1小时、1至4小时、4至6小时和6至8小时期间,通过高压液相色谱和放射免疫测定相结合的方法测量胆汁中的肽白三烯(LTC4、LTD4、LTE4和N-乙酰-LTE4)。接受抗原激发的10只大鼠均出现早期反应。其中,6只还出现了迟发反应,而2只在激发后约1小时死亡。在抗原激发后4至8小时(与迟发反应时间相对应),出现迟发反应的卵清蛋白滴注大鼠(n = 6)胆汁中排出的肽白三烯水平,比接受生理盐水滴注的卵清蛋白致敏对照大鼠(n = 6;p < 0.02)高约四倍。(摘要截短至

相似文献

1
Leukotrienes in bile during the early and the late airway responses after allergen challenge of sensitized rats.致敏大鼠过敏原激发后早期和晚期气道反应期间胆汁中的白三烯
Am Rev Respir Dis. 1993 Jan;147(1):104-10. doi: 10.1164/ajrccm/147.1.104.
2
Effects of dexamethasone on leukotriene synthesis and airway responses to antigen and leukotriene D4 in rats.地塞米松对大鼠白三烯合成及气道对抗原和白三烯D4反应的影响
Am J Respir Crit Care Med. 1995 Apr;151(4):1143-50. doi: 10.1164/ajrccm/151.4.1143.
3
Conjugates of ovalbumin and monomethoxypolyethylene glycol abolish late allergic responses and decrease IL-4 and IL-5 mRNA expression in the rat.
Pulm Pharmacol Ther. 2003;16(6):361-9. doi: 10.1016/j.pupt.2003.08.001.
4
Morphometric changes during the early airway response to allergen challenge in the rat.
Am Rev Respir Dis. 1992 Oct;146(4):1037-41. doi: 10.1164/ajrccm/146.4.1037.
5
Adoptive transfer of allergic airway responses with sensitized lymphocytes in BN rats.在BN大鼠中通过致敏淋巴细胞进行变应性气道反应的过继转移。
Am J Respir Crit Care Med. 1995 Jul;152(1):64-70. doi: 10.1164/ajrccm.152.1.7599864.
6
Late airway responses to antigen challenge in sensitized inbred rats.
Am Rev Respir Dis. 1988 May;137(5):1033-7. doi: 10.1164/ajrccm/137.5.1033.
7
Antigen-induced airway inflammation and hyper-responsiveness does not enhance airway responses to a subsequent antigen challenge in rats.抗原诱导的气道炎症和高反应性不会增强大鼠对随后抗原刺激的气道反应。
Respir Med. 2000 Jan;94(1):44-50. doi: 10.1053/rmed.1999.0713.
8
Evidence for major basic protein immunoreactivity and interleukin 5 gene activation during the late phase response in explanted airways.外植气道迟发反应期间主要碱性蛋白免疫反应性和白细胞介素5基因激活的证据。
Am J Respir Cell Mol Biol. 1996 Nov;15(5):582-9. doi: 10.1165/ajrcmb.15.5.8918365.
9
The in vivo production of peptide leukotrienes after pulmonary anaphylaxis in the rat.大鼠肺部过敏反应后肽白三烯的体内生成。
J Immunol. 1988 Nov 15;141(10):3544-50.
10
IL-2 enhances allergic airway responses in rats by increased inflammation but not through increased synthesis of cysteinyl leukotrienes.白细胞介素-2通过加剧炎症反应而非增加半胱氨酰白三烯的合成来增强大鼠的过敏性气道反应。
J Allergy Clin Immunol. 1999 Jul;104(1):145-52. doi: 10.1016/s0091-6749(99)70126-0.

引用本文的文献

1
Site of allergic airway narrowing and the influence of exogenous surfactant in the Brown Norway rat.气道变窄过敏部位及外源性表面活性剂对布朗-挪威大鼠的影响。
PLoS One. 2012;7(1):e29381. doi: 10.1371/journal.pone.0029381. Epub 2012 Jan 19.
2
A small molecule, orally active, alpha4beta1/alpha4beta7 dual antagonist reduces leukocyte infiltration and airway hyper-responsiveness in an experimental model of allergic asthma in Brown Norway rats.一种小分子、口服活性的α4β1/α4β7双重拮抗剂可减少棕色挪威大鼠过敏性哮喘实验模型中的白细胞浸润和气道高反应性。
Br J Pharmacol. 2006 Mar;147(6):661-70. doi: 10.1038/sj.bjp.0706658.
3
Mast-cell activation augments the late phase reaction in experimental immune-mediated blepharoconjunctivitis.
肥大细胞活化增强实验性免疫介导性睑结膜炎的迟发相反应。
Graefes Arch Clin Exp Ophthalmol. 2003 May;241(5):394-402. doi: 10.1007/s00417-003-0641-9. Epub 2003 Apr 4.
4
The strength of the OVA-induced airway inflammation in rats is strain dependent.卵清蛋白诱导的大鼠气道炎症强度具有品系依赖性。
Clin Exp Immunol. 2002 Sep;129(3):390-6. doi: 10.1046/j.1365-2249.2002.01938.x.
5
Involvement of cysteinyl leukotrienes in airway smooth muscle cell DNA synthesis after repeated allergen exposure in sensitized Brown Norway rats.半胱氨酰白三烯在致敏的棕色挪威大鼠反复暴露于变应原后气道平滑肌细胞DNA合成中的作用。
Br J Pharmacol. 1999 Jul;127(5):1151-8. doi: 10.1038/sj.bjp.0702669.
6
Transfer of allergic airway responses with antigen-primed CD4+ but not CD8+ T cells in brown Norway rats.在棕色挪威大鼠中,抗原致敏的CD4 +而非CD8 + T细胞介导变应性气道反应的转移。
J Clin Invest. 1995 Sep;96(3):1303-10. doi: 10.1172/JCI118165.
7
Allergen-induced airway responses in rats pretreated with Sephadex.用葡聚糖预处理的大鼠中变应原诱导的气道反应。
Agents Actions. 1993 Nov;40(3-4):141-9. doi: 10.1007/BF01984053.