Tibbitts Jay
XOMA (US) LLC, Berkeley, California 94710, USA.
Toxicol Pathol. 2003 Jan-Feb;31 Suppl:17-24. doi: 10.1080/01926230390174896.
The dog is a commonly used animal model by virtue of its size, well-characterized physiology, and ease of handling. For these reasons and others, dogs are also useful in pharmacokinetic and metabolism studies during the development of both human and veterinary pharmaceutical products. In comparison with humans, or with other animals, dogs have some unique physiologic attributes that can affect the disposition of drugs. Species differences in gastrointestinal physiology, metabolism, renal function, and protein binding can affect the correlation of the pharmacokinetics and toxicology of dogs with those of other species. With the use of relevant examples, this article will provide an introduction to characteristics of dog physiology and their impact on pharmacokinetics, metabolism, drug disposition, toxicity, and dose selection.
狗因其体型、生理特征明确以及易于处理,是常用的动物模型。基于这些及其他原因,狗在人用和兽用药品研发过程中的药代动力学和代谢研究中也很有用。与人类或其他动物相比,狗具有一些独特的生理特性,这些特性会影响药物的处置。胃肠生理学、代谢、肾功能和蛋白结合方面的种属差异会影响狗与其他种属在药代动力学和毒理学方面的相关性。本文将通过相关实例介绍狗的生理特征及其对药代动力学、代谢、药物处置、毒性和剂量选择的影响。