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降钙素原对诱导型一氧化氮合酶基因表达及一氧化氮合成的体外调节作用

In vitro modulation of inducible nitric oxide synthase gene expression and nitric oxide synthesis by procalcitonin.

作者信息

Hoffmann G, Totzke G, Seibel M, Smolny M, Wiedermann F J, Schobersberger W

机构信息

Department of Physiology I, University of Bonn, Germany.

出版信息

Crit Care Med. 2001 Jan;29(1):112-6. doi: 10.1097/00003246-200101000-00023.

Abstract

OBJECTIVE

Serum procalcitonin (PCT) concentration was recently introduced as valuable diagnostic marker for systemic bacterial infection and sepsis. At present, the cellular sources and biological properties of PCT are unclear. During sepsis and septic shock, inducible nitric oxide synthase (iNOS) gene expression is stimulated followed by the release of large amounts of nitric oxide (NO). We investigated the possible association between PCT and iNOS gene expression in an in vitro cell culture model.

DESIGN

Prospective, controlled in vitro cell culture study.

SETTING

University research laboratories.

INTERVENTIONS

Confluent rat vascular smooth muscle cells (VSMC) were incubated for 24 hrs and 48 hrs with PCT (1 ng/mL, 10 ng/mL, 100 ng/mL, 1,000 ng/mL, 5,000 ng/mL) alone or with the combination of tumor necrosis factor-alpha (TNF-alpha, 500 U/mL) plus interferon-gamma (IFN-gamma, 100 U/mL). iNOS gene expression was measured by qualitative as well as quantitative polymerase chain reaction analysis, NO release was estimated by the modified Griess method.

MEASUREMENTS AND MAIN RESULTS

PCT in increasing concentrations had no effect on iNOS gene expression and nitrite/nitrate release for 24 hrs and 48 hrs, respectively. However, PCT ameliorated TNF-alpha/IFN-gamma-induced iNOS gene expression in a dose-dependent manner (maximal inhibition at PCT 100 ng/mL by -66% for 24 hrs and -80% for 48 hrs). This was accompanied by a significantly reduced release of nitrite/nitrate into the cell culture supernatant (maximal reduction at PCT 100 ng/mL by -56% and -45% for 24 hrs and 48 hrs, respectively).

CONCLUSIONS

We conclude that recombinant PCT inhibits the iNOS-inducing effects of the proinflammatory cytokines TNF-alpha/ IFN-gamma in a dose-dependent manner. This might be a counter-regulatory mechanism directed against the large production of NO and the concomitant systemic hypotension in severe sepsis and septic shock.

摘要

目的

血清降钙素原(PCT)浓度最近被作为全身细菌感染和脓毒症的重要诊断标志物。目前,PCT的细胞来源和生物学特性尚不清楚。在脓毒症和脓毒性休克期间,诱导型一氧化氮合酶(iNOS)基因表达受到刺激,随后释放大量一氧化氮(NO)。我们在体外细胞培养模型中研究了PCT与iNOS基因表达之间可能存在的关联。

设计

前瞻性、对照体外细胞培养研究。

单位

大学研究实验室。

干预措施

将汇合的大鼠血管平滑肌细胞(VSMC)单独用PCT(1 ng/mL、10 ng/mL、100 ng/mL、1000 ng/mL、5000 ng/mL)或与肿瘤坏死因子-α(TNF-α,500 U/mL)加干扰素-γ(IFN-γ,100 U/mL)联合孵育24小时和48小时。通过定性和定量聚合酶链反应分析测量iNOS基因表达,通过改良的Griess法估计NO释放。

测量指标及主要结果

浓度递增的PCT分别在24小时和48小时对iNOS基因表达及亚硝酸盐/硝酸盐释放均无影响。然而,PCT以剂量依赖方式改善TNF-α/IFN-γ诱导的iNOS基因表达(PCT 100 ng/mL时,24小时最大抑制率为-66%,48小时为-80%)。这伴随着细胞培养上清液中亚硝酸盐/硝酸盐释放显著减少(PCT 100 ng/mL时,24小时和48小时最大减少率分别为-56%和-45%)。

结论

我们得出结论,重组PCT以剂量依赖方式抑制促炎细胞因子TNF-α/IFN-γ诱导iNOS的作用。这可能是一种针对严重脓毒症和脓毒性休克中大量NO产生及随之而来的全身低血压的反调节机制。

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