• 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

实验性肺炎球菌性中耳炎中耳积液溶菌酶的来源

Middle ear fluid lysozyme source in experimental pneumococcal otitis media.

作者信息

Nonomura N, Giebink G S, Zelterman D, Harada T, Juhn S K

机构信息

Department of Otolaryngology, School of Medicine, University of Minnesota, Minneapolis.

出版信息

Ann Otol Rhinol Laryngol. 1991 Jul;100(7):593-6. doi: 10.1177/000348949110000715.

DOI:10.1177/000348949110000715
PMID:2064274
Abstract

Middle ear infection with Streptococcus pneumoniae is important in the pathogenesis of acute and chronic otitis media, and lysozyme in middle ear fluid (MEF) is an important inflammatory mediator in this disease. To determine the source of lysozyme during the early period of acute pneumococcal otitis media, chinchillas were irradiated to induce neutropenia, and their middle ears were inoculated with heat-killed, encapsulated pneumococci. The number of inflammatory cells and concentration of lysozyme were measured in MEF between 6 and 72 hours after inoculation. In pneumococcus-inoculated ears, the mean number of inflammatory cells but not lysozyme was significantly lower in MEF from irradiated animals than that from nonirradiated animals at 6 hours. Since lysozyme accumulated in MEF before the influx of inflammatory cells in irradiated animals, the initial release of this inflammatory mediator is most likely not from inflammatory cells; and mucosal epithelial cells, the only other known source of lysozyme in the middle ear environment, were the probable source induced by the direct stimulation of pneumococci. Inflammatory cells may contribute lysozyme later in the inflammatory response, since cellular and lysozyme concentrations in irradiated and nonirradiated animals were similar between 24 and 72 hours. These results suggest that future therapeutic interventions to limit middle ear inflammation in acute otitis media may need to recognize the direct action of pneumococcal cells or their envelope components on middle ear epithelium.

摘要

肺炎链球菌引起的中耳感染在急慢性中耳炎的发病机制中具有重要作用,中耳积液(MEF)中的溶菌酶是该疾病中一种重要的炎症介质。为了确定急性肺炎球菌性中耳炎早期溶菌酶的来源,对栗鼠进行照射以诱导中性粒细胞减少,然后向它们的中耳接种热灭活的、有荚膜的肺炎球菌。在接种后6至72小时测量中耳积液中的炎症细胞数量和溶菌酶浓度。在接种肺炎球菌的耳朵中,照射动物的中耳积液中炎症细胞的平均数量在6小时时显著低于未照射动物,但溶菌酶的平均数量并非如此。由于在照射动物中,溶菌酶在炎症细胞流入之前就在中耳积液中积累,因此这种炎症介质的初始释放很可能并非来自炎症细胞;而中耳环境中溶菌酶的唯一其他已知来源——黏膜上皮细胞,很可能是由肺炎球菌的直接刺激所诱导的来源。炎症细胞可能在炎症反应后期才会释放溶菌酶,因为在24至72小时之间,照射动物和未照射动物的细胞和溶菌酶浓度相似。这些结果表明,未来旨在限制急性中耳炎中耳炎症的治疗干预措施可能需要认识到肺炎球菌细胞或其包膜成分对中耳上皮的直接作用。

相似文献

1
Middle ear fluid lysozyme source in experimental pneumococcal otitis media.实验性肺炎球菌性中耳炎中耳积液溶菌酶的来源
Ann Otol Rhinol Laryngol. 1991 Jul;100(7):593-6. doi: 10.1177/000348949110000715.
2
The contribution of pneumococcal cell wall to the pathogenesis of experimental otitis media.肺炎球菌细胞壁在实验性中耳炎发病机制中的作用。
J Infect Dis. 1988 Feb;157(2):245-55. doi: 10.1093/infdis/157.2.245.
3
Penicillin treatment accelerates middle ear inflammation in experimental pneumococcal otitis media.青霉素治疗会加速实验性肺炎球菌性中耳炎的中耳炎症。
Infect Immun. 1992 May;60(5):1908-12. doi: 10.1128/iai.60.5.1908-1912.1992.
4
Pathophysiology of Streptococcus pneumoniae otitis media: kinetics of the middle ear biochemical and cytologic host responses.
Ann Otol Rhinol Laryngol. 1991 Mar;100(3):236-43. doi: 10.1177/000348949110000313.
5
Cathepsin gene expression profile in rat acute pneumococcal otitis media.大鼠急性肺炎球菌性中耳炎中组织蛋白酶基因表达谱
Laryngoscope. 2004 Jun;114(6):1032-6. doi: 10.1097/00005537-200406000-00014.
6
Early biochemical events in pneumococcal otitis media: arachidonic acid metabolites in middle ear fluid.肺炎球菌性中耳炎的早期生化事件:中耳液中的花生四烯酸代谢产物
Ann Otol Rhinol Laryngol. 1991 May;100(5 Pt 1):385-8. doi: 10.1177/000348949110000507.
7
Biochemical pathology of otitis media with effusion.分泌性中耳炎的生化病理学
Acta Otolaryngol Suppl. 1984;414:45-51. doi: 10.3109/00016488409122881.
8
The pathogenesis of pneumococcal otitis media in chinchillas and the efficacy of vaccination in prophylaxis.栗鼠中耳肺炎球菌性中耳炎的发病机制及疫苗接种在预防中的效果。
Rev Infect Dis. 1981 Mar-Apr;3(2):342-53. doi: 10.1093/clinids/3.2.342.
9
Middle ear fluid cytokine and inflammatory cell kinetics in the chinchilla otitis media model.灰鼠中耳炎模型中中耳积液细胞因子及炎症细胞动力学
Infect Immun. 1999 Apr;67(4):1943-6. doi: 10.1128/IAI.67.4.1943-1946.1999.
10
Otitis media: the chinchilla model.中耳炎:栗鼠模型
Microb Drug Resist. 1999 Spring;5(1):57-72. doi: 10.1089/mdr.1999.5.57.

引用本文的文献

1
Peroxiredoxin-glutaredoxin and catalase promote resistance of nontypeable Haemophilus influenzae 86-028NP to oxidants and survival within neutrophil extracellular traps.过氧化物氧还蛋白-谷氧还蛋白和过氧化氢酶促进不可分型流感嗜血杆菌86-028NP对氧化剂的抗性及在中性粒细胞胞外诱捕网内的存活。
Infect Immun. 2015 Jan;83(1):239-46. doi: 10.1128/IAI.02390-14. Epub 2014 Oct 27.
2
Otitis media among high-risk populations: can probiotics inhibit Streptococcus pneumoniae colonisation and the risk of disease?高危人群中的中耳炎:益生菌能否抑制肺炎链球菌定植和发病风险?
Eur J Clin Microbiol Infect Dis. 2013 Sep;32(9):1101-10. doi: 10.1007/s10096-013-1858-0. Epub 2013 Mar 20.
3
Induction of beta defensin 2 by NTHi requires TLR2 mediated MyD88 and IRAK-TRAF6-p38MAPK signaling pathway in human middle ear epithelial cells.
在人中耳上皮细胞中,NTHi诱导β-防御素2需要TLR2介导的MyD88和IRAK-TRAF6-p38MAPK信号通路。
BMC Infect Dis. 2008 Jun 25;8:87. doi: 10.1186/1471-2334-8-87.
4
Antimicrobial activity of innate immune molecules against Streptococcus pneumoniae, Moraxella catarrhalis and nontypeable Haemophilus influenzae.天然免疫分子对肺炎链球菌、卡他莫拉菌和不可分型流感嗜血杆菌的抗菌活性。
BMC Infect Dis. 2004 May 5;4:12. doi: 10.1186/1471-2334-4-12.
5
Roles of autolysin and pneumolysin in middle ear inflammation caused by a type 3 Streptococcus pneumoniae strain in the chinchilla otitis media model.自溶素和肺炎溶血素在栗鼠中耳炎模型中由3型肺炎链球菌菌株引起的中耳炎症中的作用。
Infect Immun. 1996 Apr;64(4):1140-5. doi: 10.1128/iai.64.4.1140-1145.1996.
6
Timing of penicillin treatment influences the course of Streptococcus pneumoniae-induced middle ear inflammation.青霉素治疗的时机影响肺炎链球菌引起的中耳炎症病程。
Antimicrob Agents Chemother. 1995 Aug;39(8):1896-8. doi: 10.1128/AAC.39.8.1896.
7
Oxidative metabolic products released from polymorphonuclear leukocytes in middle ear fluid during experimental pneumococcal otitis media.实验性肺炎球菌性中耳炎期间中耳液中多形核白细胞释放的氧化代谢产物。
Infect Immun. 1991 Nov;59(11):4084-8. doi: 10.1128/iai.59.11.4084-4088.1991.
8
Penicillin treatment accelerates middle ear inflammation in experimental pneumococcal otitis media.青霉素治疗会加速实验性肺炎球菌性中耳炎的中耳炎症。
Infect Immun. 1992 May;60(5):1908-12. doi: 10.1128/iai.60.5.1908-1912.1992.