Effects of Fluid Treatment in a B. Anthracis Lethal Toxin Challenged Rat Model
Effects of Fluid Treatment in a B. Anthracis Lethal Toxin Challenged Rat Model
批准号:
7593071
负责人:
Peter Q Eichacker
金额:
$4.44万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AnimalsBacillus anthracisBacteriaBacterial InfectionsBacterial ToxinsBacterial TypingBlood PressureCatecholaminesDataDisease OutbreaksEffectivenessEscherichia coliHypoxemiaInfectionInflammatoryLifeLipopolysaccharidesLiquid substanceModelingMonoclonal AntibodiesNitric OxideNorepinephrinePathogenesisPatientsPatternPhasePlasmaPlayPurposeRattusResistanceRoleSepsisSeptic ShockShockToxinVasoconstrictor Agentsanthrax lethal factorbasecytokinehemodynamicsimprovedresponsetreatment effect
中文摘要
在美国最近爆发的炭疽杆菌感染中,对液体和血管升压剂的常规治疗耐受休克在死亡患者中很常见。在以往的研究中,尽管致死性脂多糖(LPS)和炭疽芽孢杆菌致死毒素(LeTx)对血压有相似的降压作用,但血浆细胞因子和一氧化氮水平与LeTx无关。这一数据和其他数据表明,LeTx休克的发病机制可能不同于败血症和感染性休克患者常见的细菌毒素类型。应考虑LeTx休克对常规血流动力学支持的反应是否也不同。
我们现在已经扩展了这些研究,目前正在比较血管升压剂治疗和去甲肾上腺素在用LeTx和脂多糖挑战的动物中的效果。在这些研究中,我们发现,尽管去甲肾上腺素确实在内毒素和LeTx中都会增加血压,但它可以提高前者的存活率,但不能提高后者的存活率。值得注意的是,在这些研究中,内源性儿茶酚胺、一氧化氮和炎性细胞因子,虽然随着脂多糖的攻击而显著升高,但与LeTx有关。因此,传统的血流动力学治疗在挑战脂多糖的情况下具有预期的有益效果,但与LeTx并非如此。
然而,总体而言,目前的发现对常规血流动力学支持治疗LeTx相关性休克的有效性提出了质疑。由于这种毒素在炭疽杆菌感染期间的休克中起着关键作用,因此更好地确定这些治疗方法在活体细菌感染期间的作用可能是重要的。
英文摘要
Shock resistant to conventional treatment with fluid and vasopressors was common in nonsurvivors in the recent outbreak of B. anthracis infection in the US. In prior studies, although blood pressure was reduced similarly with lethal lipopolysaccharide (LPS) and Bacillus anthracis lethal toxin (LeTx) challenges, plasma cytokine and nitric oxide levels, while increased with LPS were not with LeTx. This and other data suggests that the pathogenesis of shock with LeTx may differ from the types of bacterial toxin commonly encountered in patients with sepsis and septic shock. Whether the response of LeTx shock to conventional hemodynamic support differs as well should be considered.
We have now extended these studies and are presently comparing the effects vasopressor treatment with norepinephrine in animals challenged with LeTx versus LPS. In these studies we found that while norepinephrine does increase blood pressure with both LPS and LeTx, it improves survival with the former but not the latter toxin. Of note in these studies endogenous catecholamines, nitric oxide, and inflammatory cytokines, while markedly elevated with LPS challenge, were with LeTx. Once again therefore, a conventional hemodynamic treatment which has the expected beneficial effects with LPS challenge, does not with LeTx.
Overall however the present findings raise questions regarding the effectiveness of conventional hemodynamic support for LeTx associated shock. Since this toxin plays a key role in shock during B. anthracis better defining the role of these treatments during live bacterial infection may be important.
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