Landskroner K A, Hess P, Treiber A
Actelion Pharmaceuticals Ltd., Preclinical Drug Metabolism and Pharmacokinetics, Gewerbestrasse 16, Allschwil, CH-4123 Switzerland.
Xenobiotica. 2011 Aug;41(8):687-700. doi: 10.3109/00498254.2011.569772. Epub 2011 Apr 13.
Mechanistic approaches in drug metabolism and pharmacokinetics during drug discovery depend upon animal models to increase the understanding of the absorption and disposition of new compounds. These animal models are also important to understand the complex interplay of biochemical and physiological events, and for the ability to answer questions in a reasonable time frame while interrogating numerous chemical structures. Many animal models have been described for understanding absorption, distribution, metabolism, and excretion and this review attempts to summarise some of these models. The focus is primarily on surgical and pharmacological models for pharmacokinetic studies in rodents with special emphasis on descriptive methodologies for researchers embarking on in vivo studies. In this review, the surgical approaches include the mechanical instrumentation of anatomical structures, e.g. abdominal cavity, marginal ear vein, while pharmacological models are restricted to chemical inhibition of the cytochrome P450 enzymes and P-gp to understand hepatic metabolism or brain penetration and intestinal absorption, respectively. The purpose of this review is not to exhaustively characterise each model but to serve as a general resource for investigators interested in performing these models.
药物研发过程中药物代谢和药代动力学的机制研究方法依赖于动物模型,以增进对新化合物吸收和处置的理解。这些动物模型对于理解生化和生理事件的复杂相互作用也很重要,并且有助于在合理的时间框架内解答众多化学结构相关问题。为理解吸收、分布、代谢和排泄,人们描述了许多动物模型,本综述旨在总结其中一些模型。重点主要放在啮齿动物药代动力学研究的手术和药理模型上,特别强调为开展体内研究的研究人员提供描述性方法。在本综述中,手术方法包括对解剖结构(如腹腔、耳缘静脉)进行机械插管,而药理模型则限于分别通过化学抑制细胞色素P450酶和P-糖蛋白来理解肝脏代谢或脑内渗透以及肠道吸收。本综述的目的不是详尽描述每个模型,而是为有兴趣开展这些模型研究的研究人员提供一个通用资源。