Anthony L, Koshakji R, Wood A J
Department of Medicine, Vanderbilt University, Nashville, TN 37232.
Clin Pharmacol Ther. 1989 Sep;46(3):297-300. doi: 10.1038/clpt.1989.141.
We investigated the effect of debrisoquin on propranolol metabolism in six normal subjects who were extensive metabolizers of debrisoquin. Each subject was studied on two occasions. On the first occasion, each subject received oral propranolol (80 mg) alone; on the second occasion, 7 days later, each subject received a dose of propranolol (80 mg) 30 minutes after the administration of oral debrisoquin (40 mg). Oral propranolol clearance was reduced 33% +/- 16% (p less than 0.05) by the administration of debrisoquin. As predicted, the 4-hydroxypropranolol partial metabolic clearance was significantly (p less than 0.05) inhibited by debrisoquin. However, the side-chain oxidation pathway, as measured by naphthoxylactic acid, was also significantly (p less than 0.05) inhibited by debrisoquin. Debrisoquin administration did not change the renal clearance of any of the metabolites. These data support the usefulness of the in vivo inhibition model in the prediction of cosegregation of routes of metabolism. However, for propranolol, pathways of its metabolism that are not thought to cosegregate with debrisoquin was also inhibited.
我们研究了异喹胍对6名异喹胍广泛代谢者体内普萘洛尔代谢的影响。每位受试者均进行了两次研究。第一次,每位受试者单独口服普萘洛尔(80毫克);第二次,7天后,每位受试者在口服异喹胍(40毫克)30分钟后服用一剂普萘洛尔(80毫克)。服用异喹胍后,口服普萘洛尔的清除率降低了33%±16%(p<0.05)。正如所预测的,异喹胍显著抑制了4-羟基普萘洛尔的部分代谢清除率(p<0.05)。然而,以萘氧乳酸衡量的侧链氧化途径也被异喹胍显著抑制(p<0.05)。服用异喹胍并未改变任何代谢物的肾清除率。这些数据支持了体内抑制模型在预测代谢途径共分离方面的有用性。然而,对于普萘洛尔,其未被认为与异喹胍共分离的代谢途径也受到了抑制。