Comparative assessment for rat strain differences in metabolic profiles of 14 drugs in Wistar Han and Sprague Dawley hepatocytes. (2nd January 2021)

• Record Type: Journal Article
• Authors: Wang, Wei; Teresa, Mulder; Cai, Jingwei; Zhang, Chenghong; Wong, Susan; Yan, Zhengyin; Khojasteh, S. Cyrus; Zhang, Donglu
• Is Part Of: Xenobiotica. Volume 51:Number 1(2021)
• Page Start: 15
• Page End: 23
• Publication Date: 2021-01-02
• Subjects: Biotransformation -- metabolite -- metabolic pathway -- clearance -- Sprague Dawley rat -- Wistar Han rat; Metabolism -- Periodicals; Drugs -- Physiological effect -- Periodicals; Food additives -- Periodicals; Chemicals -- Physiological effect -- Periodicals; Biochemistry -- Periodicals; Pharmaceutical Preparations -- metabolism -- Periodicals; Metabolism -- Periodicals; 574.133
• DOI: 10.1080/00498254.2020.1795949
• Languages: English
• ISSNs: 0049-8254

Abstract

Abstract: Knowledge of inter-strain and inter-gender differences in drug metabolism studies is important for animal selection in pharmacokinetic and toxicological studies. The effects of rat strain and gender in in vitro metabolism were investigated in Sprague Dawley (SD) and Wister Han (WH) rats based on the hepatocyte metabolic profiles of 14 small molecule drugs. Similarities were found between the hepatocyte metabolic clearances of SD and WH strains, suggesting that only one strain can be confidently used for the evaluation of hepatic clearance. Neither strain of rat was preferable over the other to cover human metabolites. Higher similarities in metabolic pathways were found between the same gender than the same strain. Differences in metabolite identities, metabolite formation rates and potential biotransformation pathways were observed between SD and WH rat strains. Eleven metabolites from six drugs were "disproportionally" formed between SD and WH rats. The use of a specific rat strain model and gender for ADME and toxicity testing should, therefore, be carefully considered as metabolic profiles may differ, even though metabolic clearance was similar between SD and WH rats.