Araki Y, Tsujikawa T, Andoh A, Sasaki M, Fujiyama Y, Bamba T
Department of Internal Medicine, Nagahama Red Cross Hospital, Shiga, Japan.
Dig Liver Dis. 2000 Nov;32(8):691-8. doi: 10.1016/s1590-8658(00)80332-1.
The pathogenesis of inflammatory bowel disease is still unknown. However, it is possible that faecal bile acids influence the clinical course.
To evaluate the eliminating effects of faecal bile acids by the oral adsorbent on dextran sulphate sodium-induced rat colitis.
Rats were given 3% dextran sulphate sodium aqueous solution for 7 days, with or without concomitant administration of oral adsorbent, or the rats were given dextran sulphate sodium for 7 days, followed with or without oral adsorbent for 5 days. Macroscopic and microscopic examinations of the colons and measurement of faecal bile acids were performed. The cytotoxicity of bile salts on Caco-2 cells was also evaluated.
Oral adsorbent tended to attenuate the dextran sulphate sodium-induced colitis. Oral adsorbent was fairly effective in reducing faecal hyodeoxycholic acid concentration. A positive correlation was found between the size of the ulcer area and the faecal hyodeoxycholic acid concentration. In a cell culture study, cytotoxicity of bile acid was parallel with increasing hydrophobicity of the bile acid. However, hyodeoxycholate exhibited severe cytotoxicity, despite its hydrophilic properties.
Oral adsorbent tended to attenuate the dextran sulphate sodium-induced colitis and tended to promote the recovery process. It is possible that bile acids in the gut lumen influence the progression of dextran sulphate sodium-induced colitis and its repair process.
炎症性肠病的发病机制仍不清楚。然而,粪便胆汁酸可能会影响其临床病程。
评估口服吸附剂对葡聚糖硫酸钠诱导的大鼠结肠炎中粪便胆汁酸的清除作用。
给大鼠饮用3%葡聚糖硫酸钠水溶液7天,同时或不同时给予口服吸附剂;或者先给大鼠饮用葡聚糖硫酸钠7天,之后再给予或不给予口服吸附剂5天。对结肠进行宏观和微观检查,并测量粪便胆汁酸。还评估了胆盐对Caco-2细胞的细胞毒性。
口服吸附剂倾向于减轻葡聚糖硫酸钠诱导的结肠炎。口服吸附剂在降低粪便猪去氧胆酸浓度方面相当有效。溃疡面积大小与粪便猪去氧胆酸浓度之间存在正相关。在细胞培养研究中,胆汁酸的细胞毒性与胆汁酸疏水性增加呈平行关系。然而,猪去氧胆酸盐尽管具有亲水性,却表现出严重的细胞毒性。
口服吸附剂倾向于减轻葡聚糖硫酸钠诱导的结肠炎,并倾向于促进恢复过程。肠腔内的胆汁酸可能会影响葡聚糖硫酸钠诱导的结肠炎的进展及其修复过程。