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Development and characterization of a novel porcine model of neonatal sepsis.

机译:发展和特征的小说猪的新生儿脓毒症模型。

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摘要

Sepsis and its sequela remain a major source of morbidity and mortality in neonates despite advances in antimicrobials and aggressive supportive care. Many models of neonatal sepsis have been developed for investigating the pathophysiology of this disease and application of therapy, and a model with an infectious focus is closer to clinical reality. To establish an animal model that mimics the clinical characteristics of neonatal sepsis, the cecal devascularization and perforation procedure was implemented on 15 mixed-strain newborn piglets, which produced an infectious focus that acted as a continuous source of microorganisms to the peritoneal cavity. The mean survival time in animals with sepsis was 10.4 h (range 5.5-17.9 h), whereas all of the sham-operated control animals survived more than 24 h. Animals with sepsis showed a gradual significant decrease in the mean systemic blood pressure (mSBP; 71 +/- 3 mmHg in sepsis vs. 64 +/- 3 mmHg in control at 3 h, 38 +/- 7 mmHg in sepsis vs. 59 +/- 4 mmHg in control at 6 h, mean +/- SEM). They also showed an increase of serum levels of endotoxin (5.6 x 10 +/- 4.5 x 10 pg/mL in sepsis vs. 6.0 x 10 +/- 3.8 x 10 pg/mL in control at 6 h). Serum levels of TNF-alpha in the animals with sepsis became significantly higher than the control animals at 0 h (96 +/- 31 pg/mL in sepsis vs. 12 +/- 1 pg/mL in control) and remained significantly higher than all through the experiment. Serum levels of IL-6 in animals with sepsis showed a gradual increase (484 +/- 231 pg/mL in sepsis in its peak at 6 h vs. 24 +/- 5 pg/mL in control), however, there were no significant differences in serum IL-10 levels between the groups. Microorganisms detected in the blood of animals with sepsis were gram-negative enteric and anaerobic organisms. These results suggested that this model mimics the clinical state of neonatal sepsis and hence may have significant implications for the treatment of sepsis, including its use as a model in further investigations.
机译:脓毒症及其后遗症的主要来源在新生儿尽管发病率和死亡率抗菌素和积极的进步支持性护理。对调查有了吗这种疾病的病理生理学和应用的治疗,并与传染病模型的焦点更接近临床现实。动物模型,模拟临床新生儿败血症的特点,盲肠的devascularization和穿孔过程15日实现mixed-strain新生的小猪,产生一种传染性的关注作为吗一个连续的微生物的来源腹膜腔。与脓毒症动物为10.4 h(范围5.5 - -17.9h),而所有的sham-operated控制超过24 h。动物与动物幸存下来脓毒症显示逐渐显著下降平均系统性血压(mSBP;毫米汞柱在脓毒症和64 + / - 3毫米汞柱控制在338岁的h + / - 7毫米汞柱在脓毒症与59 + / - 4毫米汞柱控制在6 h,意思是+ / - SEM)。增加血清内毒素水平(5.6 x10 + / - 4.5 x 10 pg / mL脓毒症与6.0 x 10 + / -3.8 x 10 pg / mL控制在6 h)。血清水平动物tnf的脓毒症明显高于对照组在控制)和保持更高比所有的实验。il - 6与脓毒症动物显示一个循序渐进的增加(484 + / - 231 pg / mL败血症的顶峰6 h和24 + / - 5 pg / mL控制),然而,血清中没有明显差异il - 10水平之间的组织。动物的血液中检测到与脓毒症革兰氏阴性肠道和厌氧生物。这些结果表明,该模型模拟新生儿败血症的临床状态,因此可能有重大影响的吗脓毒症的治疗,包括它的使用作为一个模型在进一步的调查。

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