首页> 外文期刊>International journal of infectious diseases: IJID : official publication of the International Society for Infectious Diseases >Superantigen-induced multiple organ dysfunction in a toxin-concentration-controlled and sequential parameter-monitored swine sepsis model.
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Superantigen-induced multiple organ dysfunction in a toxin-concentration-controlled and sequential parameter-monitored swine sepsis model.

机译:在毒素浓度控制和顺序参数监测的猪败血症模型中,超抗原诱导的多器官功能障碍。

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OBJECTIVE: In order to examine the biological activity of low-dose and continuously infused superantigen, and to establish a superantigen-induced multiple organ dysfunction animal model, several pathophysiological parameters were sequentially monitored in a toxin-concentration-controlled pig model. METHODS: Anesthetized, mechanically ventilated and Swan-Ganz thermodilution catheter-inserted pigs were treated with toxic shock syndrome toxin-1 (TSST-1) by infusion at 2mug/kg/h for 5h. Monitoring was performed for both the infusion period and a subsequent 1-h post-infusion period. RESULTS: The serum concentration of TSST-1 was controlled so as to elevate it to a level over 1000pg/mL within 1h of initiation of infusion, and then gradually increased further and reached a plateau of about 2500pg/mL at 4h after initiation. The animals showed a significant increase in cardiac output, the intrapulmonary arteriovenous shunt ratio, and infiltration of white blood cells into the lung. Although the observed increase in pulmonary vascular resistance was not statistically significant, it did correlate with the reduction in white blood cell counts. CONCLUSION: The superantigen TSST-1 plays an important role in the pathogenesis of Gram-positive bacterial sepsis by inducing multiple organ dysfunction. Thus, this model provides the first tool to allow the simultaneous examination of the serum toxin levels and other organ parameters in a time-course manner.
机译:目的:为了检查低剂量连续输注的超抗原的生物学活性,并建立由超抗原引起的多器官功能障碍动物模型,在毒素浓度控制的猪模型中依次监测了几种病理生理参数。方法:对麻醉,机械通气和插入Swan-Ganz热稀释导管的猪,以2ug / kg / h的速度输注5毒性毒性休克综合征毒素-1(TSST-1)。监测输液时间和输液后随后的1小时。结果:控制TSST-1的血清浓度,使其在输注开始后1h内升高至1000pg / mL以上,然后逐渐升高,并在开始后4h达到稳定水平约2500pg / mL。这些动物显示出心输出量,肺内动静脉分流比以及白细胞向肺部的浸润显着增加。尽管观察到的肺血管阻力增加没有统计学意义,但确实与白细胞计数减少相关。结论:超抗原TSST-1通过诱导多器官功能障碍在革兰氏阳性细菌性败血症的发病中起重要作用。因此,该模型提供了第一个工具,允许以时程方式同时检查血清毒素水平和其他器官参数。

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