Laliberte R, Chakrabarti S, Brodeur J
J Pharmacol Exp Ther. 1977 Jan;200(1):44-51.
A study was undertaken to investigate the influence of fasting on the disposition of warfarin in rats. Fasting consisted of withholding solid food, but not water, immediately following warfarin (3 or 10 mg/kg s.c.) administration until sacrifice at different time intervals (3, 6, 12, 24 and 30 hours). Control animals were fed ad libitum. Total and unbound warfarin concentrations were measured in plasma and liver supernatant as well as unchanged warfarin and its metabolites in urine. The disposition of unbound warfarin was found to be markedly affected by fasting, especially at the 3 mg/kg dose: the disappearance rate of unbound warfarin from plasma was accelerated in fasted animals in contrast to that of total warfarin. In addition, unbound warfarin was cleared from plasma at a more rapid rate than total warfarin in both control and fasted animals. At the 10 mg/kg dose, the disposition of total and unbound warfarin was little affected by fasting. The concentration of unbound warfarin in the liver supernatant of fasted rats given warfarin, 3 mg/kg, was significantly increased at 6 and 24 hours of fasting. Plasma free fatty acids were significantly elevated starting at 6 hours, but no such difference was noticed with liver homogenate, except at 24 hours. The 24-hour urinary excretion of unchanged warfarin was higher in fasted rats, but fasting failed to produce any change in the excretion of warfarin metabolites. The results of the present investigation indicate that short periods of fasting influence the disposition of unbound warfarin without apparently modifying its biotransformation and further show the importance of plasma protein binding on the pharmacokinetics of warfarin.
进行了一项研究以调查禁食对大鼠体内华法林处置的影响。禁食包括在皮下注射华法林(3或10mg/kg)后立即停止供应固体食物,但不限制饮水,直至在不同时间间隔(3、6、12、24和30小时)处死。对照动物自由进食。测量血浆和肝脏上清液中的总华法林和游离华法林浓度,以及尿液中未改变的华法林及其代谢物。发现禁食对华法林游离部分的处置有显著影响,尤其是在3mg/kg剂量时:与总华法林相比,禁食动物血浆中游离华法林的消失速率加快。此外,在对照动物和禁食动物中,游离华法林从血浆中的清除速率均比总华法林快。在10mg/kg剂量时,禁食对总华法林和游离华法林的处置影响较小。给予3mg/kg华法林的禁食大鼠在禁食6和24小时时,肝脏上清液中游离华法林的浓度显著升高。血浆游离脂肪酸从6小时开始显著升高,但肝脏匀浆中除24小时外未观察到此类差异。禁食大鼠中未改变的华法林24小时尿排泄量较高,但禁食未对华法林代谢物的排泄产生任何影响。本研究结果表明,短时间禁食会影响游离华法林的处置,但未明显改变其生物转化,并进一步表明血浆蛋白结合对华法林药代动力学的重要性。