Luk G D, Vaughan W P, Burke P J, Baylin S B
Cancer Res. 1981 Jun;41(6):2334-7.
Diamine oxidase (DAO; EC 1.4.3.6) is an enzyme found in high activity in the mature upper villus cells of rat intestinal mucosa and only in very low activity in all other tissues except for the placenta in the pregnant rat. The present study was designed to investigate whether plasma and mucosal DAO could be used to monitor the timing and severity of injury and recovery of the intestinal mucosa after administration of the chemotherapeutic agent 1-beta-D-arabinofuranosylcytosine (ara-C). A dose of 0.3 g/kg s.c. every 8 hr for 6 doses was given to adult Lewis x Brown Norway rats. This resulted in death of the proliferating crypt cells, followed by regeneration of the mucosa from the surviving crypt cells, with recovery by Day 8. This mucosal damage and recovery was reflected by histological changes and a decrease in activity of mucosal disaccharidases and alkaline phosphatase. Both mucosal and plasma DAO levels also fell markedly to less than 10% of basal levels (N = 30, p less than 0.005) by Day 4 and recovered with a time course similar to the histological and biochemical changes indicative of injury and recovery. With increasing dosage and/or increasing duration of ara-C treatment, mucosal injury was progressive, with increasing loss of both plasma and mucosal DAO levels as compared to controls (N = 38, p less than 0.005). Plasma DAO levels in three patients with leukemia following ara-C chemotherapy decreased markedly to less than 30% of basal pretreatment levels (p less than 0.05) by Days 9 to 12, with a time course that was compatible with clinical intestinal mucosal injury. Our data document that plasma DAO levels reflect the mucosal injury and subsequent recovery after ara-C treatment in the rat and humans. Thus, plasma DAO may serve as a marker of the integrity of the intestinal mucosa after chemotherapy.
二胺氧化酶(DAO;EC 1.4.3.6)是一种在大鼠肠黏膜成熟的上部绒毛细胞中高活性存在的酶,在除怀孕大鼠胎盘外的所有其他组织中活性都非常低。本研究旨在调查血浆和黏膜DAO是否可用于监测化疗药物1-β-D-阿拉伯呋喃糖基胞嘧啶(ara-C)给药后肠黏膜损伤和恢复的时间及严重程度。对成年Lewis×Brown Norway大鼠每8小时皮下注射0.3 g/kg,共注射6剂。这导致增殖的隐窝细胞死亡,随后存活的隐窝细胞使黏膜再生,至第8天恢复。这种黏膜损伤和恢复通过组织学变化以及黏膜二糖酶和碱性磷酸酶活性降低得以体现。到第4天,黏膜和血浆DAO水平均显著下降至基础水平的10%以下(N = 30,p < 0.005),并随着与损伤和恢复相关的组织学及生化变化的时间进程而恢复。随着ara-C治疗剂量增加和/或治疗持续时间延长,黏膜损伤呈进行性加重,与对照组相比,血浆和黏膜DAO水平下降幅度增大(N = 38,p < 0.005)。3例接受ara-C化疗的白血病患者的血浆DAO水平在第9至12天显著下降至预处理基础水平的30%以下(p < 0.05),其时间进程与临床肠黏膜损伤相符。我们的数据表明,血浆DAO水平反映了ara-C治疗后大鼠和人类的肠黏膜损伤及随后的恢复情况。因此,血浆DAO可作为化疗后肠黏膜完整性的标志物。