Lillemoe K D, Kidder G W, Harmon J W, Gadacz T R, Johnson L F, Bunte R M, Hofmann A F
Dig Dis Sci. 1983 Apr;28(4):359-64. doi: 10.1007/BF01324955.
Bile acids are capable of disrupting the gastric and esophageal mucosal barriers and are known to differ in their ability to injure these mucosae. Two bile acids, chenodeoxycholic and its 7-B epimer, ursodeoxycholic, that are being used to dissolve gallbladder stones were evaluated for their damaging effects on experimental preparations of the esophageal (rabbit) and gastric (dog) mucosa. Damage was assessed by measuring indices of mucosal barrier function, including net acid flux, potential difference, and tissue resistance, before and after exposure to the taurine conjugates of these bile acids. In both the esophageal and gastric mucosa, tauroursodeoxycholic acid caused significantly less disruption of barrier function than taurochenodeoxycholic acid. These results demonstrate that minor differences in conjugated bile acid structure can cause major changes in the effects of bile acids on the upper gastrointestinal mucosa and that ursodeoxycholic acid may be the preferred bile acid for oral ingestion to dissolve gallbladder stones.
胆汁酸能够破坏胃和食管黏膜屏障,并且已知它们损伤这些黏膜的能力存在差异。对用于溶解胆囊结石的两种胆汁酸——鹅去氧胆酸及其7-β差向异构体熊去氧胆酸——对食管(兔)和胃(犬)黏膜实验制剂的损伤作用进行了评估。通过测量暴露于这些胆汁酸的牛磺酸共轭物前后的黏膜屏障功能指标,包括净酸通量、电位差和组织电阻,来评估损伤情况。在食管和胃黏膜中,牛磺熊去氧胆酸对屏障功能的破坏明显少于牛磺鹅去氧胆酸。这些结果表明,共轭胆汁酸结构上的微小差异可导致胆汁酸对上消化道黏膜作用的重大变化,并且熊去氧胆酸可能是口服用于溶解胆囊结石的首选胆汁酸。