Martin D M, Someren A O, Nasrallah S M
Gastroenterology. 1981 Oct;81(4):736-41.
Prostaglandins have been reported to exert a protective effect against short-term experimental pancreatic injury. We evaluated the protective effect of PGE2 using a model designed to maintain pancreatitis over a period of 5-10 days. Acute pancreatitis was induced by daily intraperitoneal injections of DL-ethionine in rats maintained on a protein-free diet. Test periods of 10 and 5 days (parts I and II, respectively) were employed. In parts I and II, PGE2 0.1 microgram/g body wt was given subcutaneously 30 min before ethionine. In part II, a second daily dose of PGE2 0.1 microgram/g body wt was given 7 h after ethionine. PGE2 did not protect against the weight loss, decrease in food consumption, alteration in serum amylase, pancreatic necrosis, or mortality induced by ethionine. This study indicates that the protective effect of PGE2 observed in short-term experimental pancreatitis is not reproducible in a model in which pancreatitis is maintained for 5 and 10 day periods.
据报道,前列腺素对短期实验性胰腺损伤具有保护作用。我们使用一个旨在使胰腺炎持续5至10天的模型评估了PGE2的保护作用。急性胰腺炎通过在无蛋白饮食的大鼠中每日腹腔注射DL-乙硫氨酸诱导产生。采用了10天和5天的试验期(分别为第一部分和第二部分)。在第一部分和第二部分中,在注射乙硫氨酸前30分钟皮下给予0.1微克/克体重的PGE2。在第二部分中,在注射乙硫氨酸7小时后每日再给予一次0.1微克/克体重的PGE2。PGE2未能预防由乙硫氨酸引起的体重减轻、食物摄入量减少、血清淀粉酶改变、胰腺坏死或死亡。本研究表明,在短期实验性胰腺炎中观察到的PGE2的保护作用在胰腺炎持续5天和10天的模型中无法重现。