Lloyd-Still J D, Beno D W, Uhing M R, Jiyamapa-Serna V A, Kimura R E
Department of Pediatrics, Rush Medical College, Chicago, Illinois, USA.
J Pediatr Gastroenterol Nutr. 2001 Mar;32(3):270-3. doi: 10.1097/00005176-200103000-00007.
The objective of the study was to determine whether ursodeoxycholic acid (Ursodiol) is protective against ibuprofen (IBU)-induced enteropathy.
Using the chronically catheterized rat model, IBU (60 mg/kg body weight per day) was infused via the gastric catheter twice daily. Pancreatic enzyme (PE; 10,000 U lipase/kg body weight per day) and Ursodiol (10 mg/kg body weight per day) in two doses were infused via the duodenal catheter. Rats were assigned to one of six treatment groups and were administered treatment for 20 days: control, IBU, PE, IBU + PE, IBU + Ursodiol, and IBU + PE + Ursodiol. The entire jejunum, ileum, cecum, and colon were available for histologic analysis using previously described techniques.
Addition of Ursodiol to high-dose IBU and normal doses of PE showed a significant reduction in the percentage of rats with ulcers (P < 0.05), total number of serositis events (P < 0.01), total number of severe ulcers (P < 0.001), and an absence of ulcers in the large intestine.
Ursodiol, the drug of choice for the treatment of cystic fibrosis liver disease, may offer a safe method of using high-dose IBU in these patients by ameliorating the enteropathy.
本研究的目的是确定熊去氧胆酸(熊去氧胆素)是否对布洛芬(IBU)诱发的肠病具有保护作用。
采用长期插管的大鼠模型,通过胃导管每天两次注入布洛芬(每天60毫克/千克体重)。通过十二指肠导管注入两种剂量的胰酶(PE;每天10,000单位脂肪酶/千克体重)和熊去氧胆酸(每天10毫克/千克体重)。将大鼠分为六个治疗组之一,并进行20天的治疗:对照组、IBU组、PE组、IBU + PE组、IBU + 熊去氧胆酸组和IBU + PE + 熊去氧胆酸组。使用先前描述的技术对整个空肠、回肠、盲肠和结肠进行组织学分析。
在高剂量IBU和正常剂量PE中添加熊去氧胆酸显示,溃疡大鼠百分比(P < 0.05)、浆膜炎事件总数(P < 0.01)、严重溃疡总数(P < 0.001)显著降低,且大肠无溃疡。
熊去氧胆酸是治疗囊性纤维化肝病的首选药物,通过改善肠病,可能为这些患者提供一种安全使用高剂量IBU的方法。