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Sepsis-induced acute kidney injury by standardized colon ascendens stent peritonitis in rats - a simple, reproducible animal model

机译:通过标准化结肠的败血症诱导的急性肾损伤在大鼠中升级支架腹膜炎 - 一种简单,可重复的动物模型

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Background Up to 50% of septic patients develop acute kidney injury (AKI). The pathomechanism of septic AKI is poorly understood. Therefore, we established an innovative rodent model to characterize sepsis-induced AKI by standardized colon ascendens stent peritonitis (sCASP). The model has a standardized focus of infection, an intensive care set up with monitoring of haemodynamics and oxygenation resulting in predictable impairment of renal function, AKI parameters as well as histopathology scoring. Methods Anaesthetized rats underwent the sCASP procedure, whereas sham animals were sham operated and control animals were just monitored invasively. Haemodynamic variables and blood gases were continuously measured. After 24 h, animals were reanesthetized; cardiac output (CO), inulin and PAH clearances were measured and later on kidneys were harvested; and creatinine, urea, cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) were analysed. Additional sCASP-treated animals were investigated after 3 and 9 days. Results All sCASP-treated animals survived, whilst ubiquitous peritonitis and significantly deteriorated clinical and macrohaemodynamic sepsis signs after 24 h (MAP, CO, heart rate) were obvious. Blood analyses showed increased lactate and IL-6 levels as well as leucopenia. Urine output, inulin and PAH clearance were significantly decreased in sCASP compared to sham and control. Additionally, significant increase in cystatin C and NGAL was detected. Standard parameters like serum creatinine and urea were elevated and sCASP-induced sepsis increased significantly in a time-dependent manner. The renal histopathological score of sCASP-treated animals deteriorated after 3 and 9 days. Conclusions The presented sCASP method is a standardized, reliable and reproducible method to induce septic AKI. The intensive care set up, continuous macrohaemodynamic and gas exchange monitoring, low mortality rate as well as the opportunity of detailed analyses of kidney function and impairments are advantages of this setup. Thus, our described method may serve as a new standard for experimental investigations of septic AKI.
机译:高达50%的脓毒症患者的50%发育急性肾损伤(AKI)。脓毒症Aki的尸体机制很糟糕。因此,我们建立了一种创新的啮齿动物模型,以通过标准化的冒号升起的肠溶性Aki来表征败血症诱导的胰腺腹膜炎(SCAP)。该模型具有标准化的感染焦点,一种重症监护,并进行了监测血液力学和氧化,导致肾功能的可预测损害,AKI参数以及组织病理学得分。方法无麻醉大鼠进行SCASP程序,而假动物是假手术,对照动物刚刚被侵入地监测。连续测量血液动力变量和血气。 24小时后,动物被分类化;测量心脏输出(CO),菊粉和PAH间隙,并在肾脏上被收获;分析了肌酐,尿素,尿素,胱抑素C和中性粒细胞明胶酶相关的脂素(NGAL)。在3至9天后研究了额外的SCASP处理的动物。结果所有SCASP治疗的动物都幸存下来,而24小时后普遍存在的腹膜炎和明显恶化的临床和宏观致动力败血症症状明显。血液分析显示乳酸和IL-6水平增加以及白细胞。与假和控制相比,SCAP中尿量输出,菊粉和PAH间隙显着降低。另外,检测到胱抑素C和NGAL的显着增加。血清肌酐和尿素等标准参数升高,SCASP诱导的败血症以时间依赖的方式显着增加。 Scasp治疗的动物的肾组织病理学分数在3至9天后恶化。结论所提出的SCASP方法是一种标准化,可靠和可重复的方法,用于诱导脓毒症AKI。重症监护设置,连续的宏观致动力学和气体交流监测,低死亡率以及肾功能和损伤详细分析的机会是该设置的优势。因此,我们所描述的方法可以作为脓毒症AKI的实验研究的新标准。

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