Department of Integrated Diagnostics & Therapeutics, National Taiwan University Hospital; Renal Division, Department of Internal Medicine, National Taiwan University Hospital; Graduate Institute of Physiology, National Taiwan University College of Medicine.
Department of Integrated Diagnostics & Therapeutics, National Taiwan University Hospital; Renal Division, Department of Internal Medicine, National Taiwan University Hospital; Graduate Institute of Physiology, National Taiwan University College of Medicine;
J Vis Exp. 2022 Jun 10(184). doi: 10.3791/63901.
Peritoneal fibrosis can occur in patients undergoing peritoneal dialysis (PD), and patients with severe peritoneal fibrosis have high morbidity and mortality. Peritonitis, high-glucose peritoneal dialysis fluid, and a long period of PD precipitate the onset of peritoneal fibrosis. An animal study of peritoneal fibrosis is needed due to the limitations of human and in vitro studies. However, most animal models do not mimic clinical conditions. To study peritoneal fibrosis, we developed a clinically relevant murine model by implanting a peritoneal catheter and injecting 2.5% high-glucose PD fluid plus 20 mM methylglyoxal (MGO) into the peritoneal cavity daily for 21 days. Implantation of the peritoneal catheter avoids peritoneal injury by needles and mimics clinical PD patients. Immunofluorescence staining showed that myofibroblasts accumulated in the fibrotic peritoneum. The experimental group had lower ultrafiltration volume and peritoneal membrane transport function (peritoneal equilibration test). In this article, we provide a detailed protocol of the model.
腹膜纤维化可发生于腹膜透析(peritoneal dialysis,PD)患者中,且严重腹膜纤维化患者具有较高的发病率和死亡率。腹膜炎、高糖腹透液和长时间 PD 会促使腹膜纤维化的发生。由于受到人体和体外研究的局限性影响,需要开展腹膜纤维化的动物研究。然而,大多数动物模型并不能模拟临床状况。为了研究腹膜纤维化,我们通过植入腹膜导管并每天向腹腔内注射 2.5%高糖 PD 液加 20mM 甲基乙二醛(methylglyoxal,MGO)来建立一种与临床相关的小鼠模型,共持续 21 天。腹膜导管的植入避免了针引起的腹膜损伤,并模拟了临床 PD 患者。免疫荧光染色显示肌成纤维细胞在纤维化的腹膜中聚集。实验组超滤量和腹膜转运功能(腹膜平衡试验)较低。本文提供了该模型的详细方案。