Kim S H, Shidoji Y, Hosoya N
Department of Biochemistry and Nutrition, School of Health Sciences, Faculty of Medicine, University of Tokyo, Japan.
Jikken Dobutsu. 1988 Jan;37(1):7-12. doi: 10.1538/expanim1978.37.1_7.
Alkaline phosphatase (ALP) activity in fecal excretions was measured in male Wistar rats. Total daily ALP activity in fecal extracts was 133.1 +/- 21.2 mumoles/min per rat weighing approximately 150 g. We found that 63.7% of the fecal ALP activity was inhibited by 30 mM L-phenylalanine (L-Phe), a specific inhibitor for intestinal ALP. As body weight increased from 150 g to 300 g, total daily ALP activity in fecal extracts decreased rapidly to 33.7 +/- 6.08 mumoles/min/rat. However, the percentage of L-Phe-sensitive ALP to total enzyme activity was less variable (40-65%) in the growing rats. Cysteamine-HCl, an ulcerogenic drug, was injected subcutaneously to adult rats (300 g b. w) at a dosage of 400 mg/kg. b. w. Daily excretion of L-Phe-sensitive ALP in fecal extracts decreased to one-third 2 days after injection. Afterwards, a steep and transient increase in the enzyme activity was detected in fecal extracts between days 4 and 7 after injection. ALP activity in fecal excretions may be a clinical indicator of duodenal mucosal damage.
在雄性Wistar大鼠中测量了粪便排泄物中的碱性磷酸酶(ALP)活性。粪便提取物中每日总ALP活性为每只体重约150克的大鼠133.1±21.2微摩尔/分钟。我们发现,粪便ALP活性的63.7%被30 mM L-苯丙氨酸(L-Phe)抑制,L-Phe是肠道ALP的特异性抑制剂。随着体重从150克增加到300克,粪便提取物中每日总ALP活性迅速下降至33.7±6.08微摩尔/分钟/大鼠。然而,在生长中的大鼠中,L-Phe敏感的ALP占总酶活性的百分比变化较小(40-65%)。将致溃疡药物半胱胺盐酸盐以400毫克/千克体重的剂量皮下注射给成年大鼠(体重300克)。注射后2天,粪便提取物中L-Phe敏感的ALP每日排泄量降至三分之一。此后,在注射后第4天至第7天之间,粪便提取物中检测到酶活性急剧且短暂的增加。粪便排泄物中的ALP活性可能是十二指肠黏膜损伤的临床指标。