慢性摄取牙龈卟啉单胞菌诱导小鼠全身一氧化氮反应。

A Nemec, Z Pavlica, D A Crossley, M Sentjurc, A Jerin, D Erzen, M Vrecl, G Majdic, I Zdovc, M Petelin, U Skaleric
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引用次数: 8

摘要

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

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.

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