Thomas D W, Henton D H
Digestion. 1985;31(2-3):82-8. doi: 10.1159/000199184.
Fecal alkaline phosphatase excretion was evaluated as a marker for intestinal damage in rats. Animals received either intraperitoneal bleomycin or saline. Controls were pair-fed with animals in the bleomycin group throughout the study. Both groups demonstrated similar patterns of fecal alkaline phosphatase excretion. There was, however, marked daily variability of fecal enzymatic activity. Fecal alkaline phosphatase excretion was largely composed of intestinal alkaline phosphatase, which was characterized by enzymatic inhibition with L-phenylalanine. Dietary intake as well as daily fecal output and protein excretion were reduced immediately following bleomycin injections and gradually increased to baseline values by 7 days. It appeared that both the direct toxic effects of bleomycin and dietary intake influenced fecal alkaline phosphatase excretion. Routine clinical application of this assay may be limited because of the number of factors which may affect its excretion.
粪便碱性磷酸酶排泄被评估为大鼠肠道损伤的一个标志物。动物接受腹腔注射博来霉素或生理盐水。在整个研究过程中,对照组与博来霉素组的动物进行配对饲养。两组粪便碱性磷酸酶排泄模式相似。然而,粪便酶活性存在明显的每日变化。粪便碱性磷酸酶排泄主要由肠道碱性磷酸酶组成,其特征是受L - 苯丙氨酸的酶抑制作用。博来霉素注射后,饮食摄入量以及每日粪便排出量和蛋白质排泄立即减少,并在7天内逐渐增加至基线值。似乎博来霉素的直接毒性作用和饮食摄入量都影响粪便碱性磷酸酶排泄。由于可能影响其排泄的因素数量较多,该检测方法的常规临床应用可能受到限制。