Hamilton R D, Wynalda M A, Fitzpatrick F A, Teagarden D L, Hamdy A H, Snider B G, Weed S D, Stringfellow D A
J Interferon Res. 1982;2(3):317-27. doi: 10.1089/jir.1982.2.317.
Using a high-performance liquid chromatographic assay, these studies attempted to correlate circulating levels of 2-amino-5-bromo-6-phenyl-4(3H)-pyrimidinone (ABPP) with the serum interferon response induced in mice, cats, dogs, cattle, and rabbits. The order of greatest sensitivity for interferon induction by ABPP was mice greater than cats greater than dogs greater than cattle greater than rabbits. Experiments to date indicate that the circulating drug levels associated with a detectable interferon response were 10-15 microgram/ml (mice), 15-30 micrograms/ml (cats and dogs), and 30-50 micrograms/ml (cattle). Whereas rabbits produced large amounts (greater than 10(4) units/ml) of interferon when induced with Newcastle disease virus, we could not demonstrate unequivocally that rabbits were induced by ABPP even when circulating drug levels reached 50 micrograms/ml, or greater. We also observed differences in the pharmacokinetics of ABPP in the different species which may contribute to the differences described for the interferon responses. The data point out the need for cautious selection of animal models for preclinical efficacy evaluation and cautious extrapolation of data from preclinical studies to eventual clinical evaluation.
利用高效液相色谱分析法,这些研究试图将2-氨基-5-溴-6-苯基-4(3H)-嘧啶酮(ABPP)的循环水平与在小鼠、猫、狗、牛和兔子中诱导的血清干扰素反应关联起来。ABPP诱导干扰素的敏感性顺序为小鼠>猫>狗>牛>兔子。迄今为止的实验表明,与可检测到的干扰素反应相关的循环药物水平在小鼠中为10 - 15微克/毫升,在猫和狗中为15 - 30微克/毫升,在牛中为30 - 50微克/毫升。虽然用新城疫病毒诱导时兔子会产生大量(>10⁴单位/毫升)的干扰素,但即使循环药物水平达到50微克/毫升或更高,我们也无法明确证明兔子能被ABPP诱导。我们还观察到ABPP在不同物种中的药代动力学存在差异,这可能导致了所描述的干扰素反应差异。这些数据指出在临床前疗效评估中谨慎选择动物模型以及谨慎地将临床前研究数据外推至最终临床评估的必要性。