Wieczorowska K, Khanna R, Moore H L, Nolph K D, Twardowski Z J
Department of Pathophysiology, University Medical School of Poznan, Poland.
Adv Perit Dial. 1995;11:48-51.
The aim of this study was to establish a rat model of peritoneal fibrosis. After insertion of peritoneal catheters into 18 rats, the rats were divided into three groups. All animals were dialyzed twice a day with 4.25% Dianeal containing heparin. Group 1 rats (control) received antibiotics (vancomycin and gentamicin) in each exchange: group 2 rats were inoculated with Escherichia coli (5 x 10(6) in 5 mL of saline) at the beginning of the study; group 3 rats were treated with antibiotics after Escherichia coli inoculation; they also received a second inoculation of Escherichia coli after the second week of the study. By the end of the second week, group 2 rats were sacrificed because of catheter problems. Group 1 and 3 rats were sacrificed after 4 weeks of dialysis. A weekly peritoneal equilibration test (PET) was performed in each rat. The comparison of the PET results from the beginning and end of the study showed an increased permeability to glucose (p < 0.05) and total protein (p < 0.05) in group 3, which was not noted in group 1. In histology samples there was only delicate fibrosis with cellular infiltration in the peritoneum in group 1 rats. These changes were much more prominent in group 3 rats. This study suggests that E. coli peritonitis causes peritoneal fibrosis in rats, but to have a sclerosing encapsulating peritonitis (SEP) model this experiment must be carried out for a longer time.
本研究的目的是建立大鼠腹膜纤维化模型。将腹膜导管插入18只大鼠体内后,将大鼠分为三组。所有动物每天用含肝素的4.25% 艾考糊精透析两次。第1组大鼠(对照组)每次换液时接受抗生素(万古霉素和庆大霉素)治疗;第2组大鼠在研究开始时接种大肠杆菌(5×10⁶个菌,溶于5 mL盐水中);第3组大鼠在接种大肠杆菌后接受抗生素治疗;在研究的第二周后,它们还接受了第二次大肠杆菌接种。到第二周结束时,第2组大鼠因导管问题被处死。第1组和第3组大鼠在透析4周后被处死。每周对每只大鼠进行一次腹膜平衡试验(PET)。研究开始和结束时PET结果的比较显示,第3组葡萄糖通透性(p<0.05)和总蛋白通透性(p<0.05)增加,而第1组未观察到这种情况。在组织学样本中,第1组大鼠腹膜仅有轻微纤维化伴细胞浸润。这些变化在第3组大鼠中更为明显。本研究表明,大肠杆菌性腹膜炎可导致大鼠腹膜纤维化,但要建立硬化包裹性腹膜炎(SEP)模型,本实验必须进行更长时间。