Chronic ingestion of Porphyromonas gingivalis induces systemic nitric oxide response in mice.

A Nemec, Z Pavlica, D A Crossley, M Sentjurc, A Jerin, D Erzen, M Vrecl, G Majdic, I Zdovc, M Petelin, U Skaleric
{"title":"Chronic ingestion of Porphyromonas gingivalis induces systemic nitric oxide response in mice.","authors":"A Nemec,&nbsp;Z Pavlica,&nbsp;D A Crossley,&nbsp;M Sentjurc,&nbsp;A Jerin,&nbsp;D Erzen,&nbsp;M Vrecl,&nbsp;G Majdic,&nbsp;I Zdovc,&nbsp;M Petelin,&nbsp;U Skaleric","doi":"10.1111/j.1399-302X.2008.00496.x","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Porphyromonas gingivalis induces nitric oxide (NO) production in various cells, systemic NO elevation being expected in chronic oral challenge.</p><p><strong>Methods: </strong>Groups of BALB/c mice were inoculated orally with either live P. gingivalis ATCC 33277 or sterile broth on days 0, 2 and 4, with or without later administration of the inducible nitric oxide synthase (iNOS) inhibitor 1400W. Plasma and tissues were harvested on day 42 for assays of tumor necrosis factor-alpha (TNF-alpha), nitrite and nitrate (NOx) and tissue NO, or histology and iNOS immunohistochemistry.</p><p><strong>Results: </strong>No signs of gingivitis were observed, but plasma NOx was significantly elevated (P = 0.028) as was TNF-alpha (P = 0.079) in P. gingivalis-inoculated animals compared with controls, NOx being reduced when 1400W was used. NO production in organs showed a similar trend, with significant elevation in liver (P = 0.017) and kidneys (P = 0.027), whereas concomitant treatment of inoculated animals with 1400W caused significant reductions in NO in aorta (P = 0.008) and kidneys (P = 0.046). Sham-inoculated 1400W-treated animals had significantly increased plasma NOx (P = 0.004) and liver NO (P = 0.04). NOx in plasma correlated significantly with NO production in lungs (0.35, P = 0.032) and kidneys (0.47, P = 0.003). Immunohistochemistry demonstrated iNOS activity in many tissues in all groups.</p><p><strong>Conclusion: </strong>Repeated oral administration of P. gingivalis induced systemic NO and NOx production in mice, probably by activating iNOS as suggested by the response to 1400W.</p>","PeriodicalId":19630,"journal":{"name":"Oral microbiology and immunology","volume":"24 3","pages":"204-10"},"PeriodicalIF":0.0000,"publicationDate":"2009-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1399-302X.2008.00496.x","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral microbiology and immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1399-302X.2008.00496.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8

Abstract

Introduction: Porphyromonas gingivalis induces nitric oxide (NO) production in various cells, systemic NO elevation being expected in chronic oral challenge.

Methods: Groups of BALB/c mice were inoculated orally with either live P. gingivalis ATCC 33277 or sterile broth on days 0, 2 and 4, with or without later administration of the inducible nitric oxide synthase (iNOS) inhibitor 1400W. Plasma and tissues were harvested on day 42 for assays of tumor necrosis factor-alpha (TNF-alpha), nitrite and nitrate (NOx) and tissue NO, or histology and iNOS immunohistochemistry.

Results: No signs of gingivitis were observed, but plasma NOx was significantly elevated (P = 0.028) as was TNF-alpha (P = 0.079) in P. gingivalis-inoculated animals compared with controls, NOx being reduced when 1400W was used. NO production in organs showed a similar trend, with significant elevation in liver (P = 0.017) and kidneys (P = 0.027), whereas concomitant treatment of inoculated animals with 1400W caused significant reductions in NO in aorta (P = 0.008) and kidneys (P = 0.046). Sham-inoculated 1400W-treated animals had significantly increased plasma NOx (P = 0.004) and liver NO (P = 0.04). NOx in plasma correlated significantly with NO production in lungs (0.35, P = 0.032) and kidneys (0.47, P = 0.003). Immunohistochemistry demonstrated iNOS activity in many tissues in all groups.

Conclusion: Repeated oral administration of P. gingivalis induced systemic NO and NOx production in mice, probably by activating iNOS as suggested by the response to 1400W.

慢性摄取牙龈卟啉单胞菌诱导小鼠全身一氧化氮反应。
简介:牙龈卟啉单胞菌诱导各种细胞产生一氧化氮(NO),在慢性口腔感染中预期全身NO升高。方法:各组BALB/c小鼠分别于第0、2、4天口服活的牙龈假单胞菌ATCC 33277或无菌肉汤,随后分别给予或不给予诱导型一氧化氮合酶(iNOS)抑制剂1400W。第42天采集血浆和组织,进行肿瘤坏死因子- α (tnf - α)、亚硝酸盐和硝酸盐(NOx)、组织NO、组织组织学和iNOS免疫组化检测。结果:与对照组相比,接种牙龈P.菌组未出现牙龈炎的症状,但血浆NOx和tnf - α明显升高(P = 0.028),使用1400W时NOx降低(P = 0.079)。肝脏(P = 0.017)和肾脏(P = 0.027)的一氧化氮产量显著升高,而同时接种1400W的动物主动脉(P = 0.008)和肾脏(P = 0.046)的一氧化氮含量显著降低。假接种1400w处理的动物血浆NOx (P = 0.004)和肝脏NO (P = 0.04)显著升高。血浆中NOx与肺(0.35,P = 0.032)和肾脏(0.47,P = 0.003)的NO生成显著相关。免疫组化显示,在所有组的许多组织中都有iNOS活性。结论:反复口服牙龈假单胞菌可诱导小鼠产生全身NO和NOx,可能是通过激活iNOS引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信