Moser J, Bagchi D, Akubue P I, Stohs S J
School of Pharmacy and Allied Health, Creighton University, Omaha, NE 68178.
Alcohol Alcohol. 1993 May;28(3):287-95.
Recent studies have shown that xenobiotics which induce oxidative stress result in an increased production and excretion of acetaldehyde (ACT), formaldehyde (FA), acetone (ACON) and malondialdehyde (MDA) in the urine of rats. We have therefore examined the effect of acute and chronic ethanol administration on the excretion of these four lipid metabolites in female Sprague-Dawley rats. Urine samples were collected over dry ice for 6 hr time periods. Aliquots of urine were derivatized with 2,4-dinitrophenylhydrazine HCl, and extracted with n-pentane. High pressure lipid chromatogrpahy (HPLC) was used to quantitate and the hydrazones of the four lipid metabolite products. Following a single, oral, acute dose of 5 g ethanol/kg, urinary excretion of ACT increased approximately 5.8-fold from 6 to 12 hr posttreatment, and decreased thereafter. FA excretion decreased by approximately 50% from 0 to 12 hr, returned to control values in the 18-24 hr urine samples, and was 1.3-fold greater than control values at 42-48 hr. ACON increased 3.1-fold over control values from 0 to 30 hr and remained elevated throughout the remaining 18 hr of the study. The excretion of MDA increased approximately 1.5-fold from 18 to 36 hr, then remained constant through the 48 hr time point. In a separate series of experiments, a chronic oral dose of 0.5 g ethanol/kg was administered to rats for 10 consecutive days and the urinary excretion of the lipid metabolites MDA, FA, ACT and ACON was examined for 11 days, beginning with the first day of ethanol administration.(ABSTRACT TRUNCATED AT 250 WORDS)
近期研究表明,诱导氧化应激的外源性物质会导致大鼠尿液中乙醛(ACT)、甲醛(FA)、丙酮(ACON)和丙二醛(MDA)的生成及排泄增加。因此,我们研究了急性和慢性给予乙醇对雌性斯普拉格 - 道利大鼠这四种脂质代谢产物排泄的影响。在干冰上收集尿液样本,每次收集6小时。尿液等分试样用盐酸2,4 - 二硝基苯肼衍生化,并用正戊烷萃取。采用高压脂质色谱法(HPLC)对四种脂质代谢产物的腙进行定量。单次口服5 g乙醇/千克的急性剂量后,ACT的尿排泄量在治疗后6至12小时增加了约5.8倍,此后下降。FA排泄量在0至12小时减少了约50%,在18 - 24小时的尿液样本中恢复到对照值,在42 - 48小时比对照值高1.3倍。ACON在0至30小时比对照值增加了3.1倍,并且在研究剩余的18小时内一直保持升高。MDA的排泄量在18至36小时增加了约1.5倍,然后在48小时时间点保持恒定。在另一系列实验中,对大鼠连续10天给予0.5 g乙醇/千克的慢性口服剂量,并从给予乙醇的第一天开始的11天内检测脂质代谢产物MDA、FA、ACT和ACON的尿排泄情况。(摘要截断于250字)