Zovko D, Loff S, Dzakovic A, Kränzlin B, Hohl H P, Grün S, Waag K L
Kinderchirurgische Klinik, Fakultät für Klinische Medizin Mannheim, Universität Heidelberg, Germany.
Res Exp Med (Berl). 1996;196(4):235-42. doi: 10.1007/BF02576846.
A rabbit model for long-term total parenteral nutrition (TPN), specially provided with cholecystostomy tube, was designed to investigate further aspects of TPN-associated cholestasis (TPN-AC). Modified surgical procedures concerning vascular access, cholecystostomy tube implantation and authors' original modalities for prolonged infusion management in the rabbit were used. Continuous TPN was performed in 30 young rabbits. Five animals died during the experiment (16.6%) and were excluded from final evaluation. Twenty-five rabbits were successfully maintained on continuous TPN for 28 days without restraint, having a cholecystostomy tube implanted 1 week after initiation of TPN. The collection of blood samples and daily parenteral administration of drugs were simply accomplished via a central venous catheter. At the same time the cholecystostomy tube enabled us to perform daily bile sampling. Saline irrigation of the biliary tree could be carried out in conscious animals maintained on TPN. A 4-week duration of TPN in this rabbit model made it possible for the first time to accomplish serial liver biopsies in order to verify the evolution of histologic changes in TPN-related hepatic dysfunction and possible effects of surgical and medical treatment. A preliminary analysis of operative findings and histology was carried out. An enlarged gallbladder containing hyperviscous bile was found in 80% of the animals 1 week after initiation of TPN. At this time it was possible to observe the first histologic changes consistent with TPN-associated hepatic disease, such as moderate to severe hepatocyte degeneration and portal inflammation. Biliary sludge was seen after 3 weeks of TPN in 70% of the rabbits, as well as a subsequent progression of TPN-associated histologic findings. Portal fibrosis and fatty liver degeneration occurred in 50% of the rabbits and bile duct proliferation in all animals. After 4 weeks of TPN (at autopsy) gallstones were found in 20% of TPN animals, as well as further progression of bile duct proliferation and fibrosis. Our first experiences with this model and preliminary results suggest that this concept offers new possibilities for further elucidation of TPN-associated hepatic dysfunction.
设计了一种长期全胃肠外营养(TPN)的兔模型,特别配备胆囊造瘘管,以进一步研究TPN相关胆汁淤积(TPN-AC)的其他方面。采用了有关血管通路、胆囊造瘘管植入的改良手术程序以及作者在兔中长期输液管理的原始方法。对30只幼兔进行持续TPN。实验过程中有5只动物死亡(16.6%),被排除在最终评估之外。25只兔子成功维持持续TPN 28天,无限制,在TPN开始1周后植入胆囊造瘘管。通过中心静脉导管简单地完成血样采集和每日药物胃肠外给药。同时,胆囊造瘘管使我们能够每日进行胆汁采样。在接受TPN的清醒动物中可以进行胆道树的盐水冲洗。在这个兔模型中进行4周的TPN首次使得能够完成系列肝活检,以验证TPN相关肝功能障碍的组织学变化演变以及手术和药物治疗的可能效果。对手术发现和组织学进行了初步分析。在TPN开始1周后,80%的动物发现胆囊增大,胆汁黏稠。此时可以观察到与TPN相关肝病一致的首批组织学变化,如中度至重度肝细胞变性和门脉炎症。TPN 3周后,70%的兔子出现胆泥,以及TPN相关组织学发现的后续进展。50%的兔子出现门脉纤维化和脂肪肝变性,所有动物均出现胆管增生。TPN 4周后(尸检时),20%的TPN动物发现胆结石,以及胆管增生和纤维化的进一步进展。我们对该模型的首次经验和初步结果表明,这一概念为进一步阐明TPN相关肝功能障碍提供了新的可能性。