Published online Mar 14, 2024. doi: 10.3748/wjg.v30.i10.1420
Peer-review started: October 17, 2023
First decision: January 15, 2024
Revised: January 17, 2024
Accepted: February 21, 2024
Article in press: February 21, 2024
Published online: March 14, 2024
Processing time: 149 Days and 12.7 Hours
Pancreaticobiliary maljunction (PBM) is the main hypothesis of choledochal cyst (CC). However, accumulating clinical evidence suggests that PBM cannot fully explain the pathogenesis of CC. Previously reported animal models, including models of anastomosis of the pancreatic and biliary ducts, models of complete ligation of the lower segment of the common bile duct, have been unable to adequately support basic researches on CCs.
Satisfactory outcomes achieved with current surgical techniques for CCs have led to a pause in basic research on the pathogenesis of CCs. Thus, we need appropriate animal models of CCs to further basic researches.
To establish a stable and repeatable animal model of CC based on partial ligation of the bile duct to investigate the pathogenesis of CCs.
Specific pathogen-free female SD rats were randomly allocated to a surgical group (partial ligation of the bile duct), sham surgical group, or control group. The partial ligation of the bile duct was performed by ligating a 1 mL needle and the bile duct together, followed by the careful removal of the needle after tightening the absorbable suture. The reliability of the model was confirmed through measurements of serum biochemical indices, the morphology of common bile duct and molecular biology experiments in rat and human tissues.
All 84 rats survived to the time of dissection. Rats in the surgical group (groups A-C) showed varying degrees of dilation of the common bile ducts with slight damage to the liver and those in the sham surgical and control groups (groups D-G) showed no dilation of the common bile ducts. The changing trends of biochemical indexes indicated that the partially ligated bile ducts experienced a pathological process of recanalization after incomplete obstruction of the distal bile duct. And the reliability of the model was also confirmed by molecular biology experiments in rat and human tissues.
The model of partial ligation of the bile duct of juvenile rats could morphologically simulate the cystic or fusiform CCs. This stable and repeatable model was more consistent with the natural disease course of CC formation than complete ligation which may assist in the basic researches of CCs.
We hope our partial ligation of the bile duct of juvenile rats can promote the basic research of CCs and provide a reliable animal model for further research on the formation of cystic CCs or fusiform CCs.