Prasad K V, Sivakumar B, Narasinga Rao B S
Contraception. 1979 Dec;20(6):619-32. doi: 10.1016/s0010-7824(79)80040-2.
The pharmacokinetics of norethindrone (NET) were studied in adult female rabbits and rhesus monkeys with a view to developing an animal model closely resembling humans in the handling of NET. Plasma levels of NET were determined in rabbits and monkeys after administering either labelled NET or a NET minipill. Pharmacokinetic parameters were evaluated by using a two-compartment open model and by graphical and regression analysis of plasma NET data. In rabbits, the drug absorption was found to be rapid and NET peak levels were attained within 0.5 to 1.0 hour. The clearance half-lives were 1.3 hours for 'alpha' and 10.0 hours for 'beta'. In monkeys, plasma NET values showed an inconsistent pattern and the approximate t 1/2 was found to lie between 4 and 6 hours. The observed pharmacokinetics of NET in rabbits rather than in monkeys were closer to those in humans. On this basis, it would appear that the rabbit is a suitable animal model for studying effects of nutritional factors on the pharmacokinetics of NET.
为了建立一个在炔诺酮(NET)处理方面与人类极为相似的动物模型,对成年雌性家兔和恒河猴的炔诺酮药代动力学进行了研究。在给予标记的炔诺酮或炔诺酮微型避孕丸后,测定家兔和猴子体内的血浆炔诺酮水平。采用二室开放模型并通过对血浆炔诺酮数据进行图形分析和回归分析来评估药代动力学参数。在家兔中,发现药物吸收迅速,在0.5至1.0小时内达到炔诺酮峰值水平。“α”相清除半衰期为1.3小时,“β”相为10.0小时。在猴子中,血浆炔诺酮值呈现出不一致的模式,发现近似t1/2在4至6小时之间。在家兔而非猴子中观察到的炔诺酮药代动力学更接近人类。在此基础上,家兔似乎是研究营养因素对炔诺酮药代动力学影响的合适动物模型。