Schäfer S G, Fichtl B, Doering W
Biopharm Drug Dispos. 1984 Apr-Jun;5(2):163-8. doi: 10.1002/bdd.2510050209.
Following i.v. injection of digoxin (10 micrograms kg-1) the ratio between digoxin concentrations in the lumen of jejunal loops perfused in situ and in plasma (L/P) of guinea pigs increased linearly with time. After 3 h, L/P was 8.7, indicating net secretion of digoxin against a concentration gradient. In quinidine treated animals (100 mg kg-1 p.o., 2 h before experiment) both the L/P ratio (5.7; p less than 0.01) and the digoxin content of jejunal tissue (-32 per cent; p less than 0.01) were markedly reduced. It is suggested that quinidine reduces the extrarenal clearance of digoxin at least in part by inhibiting the intestinal secretion of this glycoside.
静脉注射地高辛(10微克/千克)后,豚鼠原位灌注的空肠肠腔与血浆中地高辛浓度之比(L/P)随时间呈线性增加。3小时后,L/P为8.7,表明地高辛逆浓度梯度进行净分泌。在奎尼丁处理的动物中(实验前2小时口服100毫克/千克),L/P比值(5.7;p<0.01)和空肠组织中的地高辛含量(-32%;p<0.01)均显著降低。提示奎尼丁至少部分通过抑制这种糖苷的肠道分泌来降低地高辛的肾外清除率。