Koponen Markus, Rysä Jaana, Ruotsalainen Anna-Kaisa, Kärkkäinen Olli, Juvonen Risto O
School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, Yliopistonranta 1, 70210 Kuopio, Finland.
Finnish Safety and Chemicals Agency, PL 66 00521, Helsinki, Finland.
J Nutr Metab. 2023 Mar 31;2023:5599789. doi: 10.1155/2023/5599789. eCollection 2023.
Consumption of a Western diet is an important risk factor for several chronic diseases including nonalcoholic fatty liver disease (NAFLD), but its effect on the xenobiotic metabolizing enzyme activities in the liver has been studied incompletely. In this study, male LDLrApoB mice were fed with Western diet (WD) or a standard diet for five months to reveal the effects on drug metabolism such as cytochrome P450 (CYP) oxidation and conjugation activities in the liver. Hepatic steatosis, lobular inflammation, and early fibrosis were observed in WD fed mice, but not in chow diet control mice. When compared to the controls, the WD-fed mice had significantly decreased protein-normalized CYP probe activities of 7-ethoxyresorufinO-deethylation (52%), coumarin 7-hydroxylation (26%), 7-hydroxylation of 3-(3-fluoro-4-hydroxyphenyl)-6-methoxycoumarin (70%), 7-hydroxylation of 3-(4-trifluoromethoxyphenyl)-6-methoxycoumarin (78%), 7-hydroxylation of 3-(3-methoxyphenyl)coumarin (81%), and pentoxyresorufin O-depentylation (66%). Increased activity was seen significantly in sulfonation of 3-(4-methylphenyl)-7-hydroxycoumarin (289%) and cytosol catechol O-methyltranferase (COMT, 148%) in the WD group when compared to the controls. In conclusion, the WD-induced steatosis in male LDLrApoB mice was associated with decreased CYP oxidation reactions but had no clear effects on conjugation reactions of glucuronidation, sulfonation, and cytosolic catechol O-methylation. Consequently, the WD may decrease the metabolic elimination of drugs compared to healthier low-fat diets.
西方饮食是包括非酒精性脂肪性肝病(NAFLD)在内的几种慢性疾病的重要风险因素,但其对肝脏中异源物质代谢酶活性的影响尚未得到充分研究。在本研究中,雄性LDLrApoB小鼠分别喂食西方饮食(WD)或标准饮食五个月,以揭示其对肝脏中药物代谢的影响,如细胞色素P450(CYP)氧化和结合活性。WD喂养的小鼠出现了肝脂肪变性、小叶炎症和早期纤维化,而普通饮食对照组小鼠未出现这些情况。与对照组相比,WD喂养的小鼠中,7-乙氧基试卤灵O-脱乙基化(52%)、香豆素7-羟基化(26%)、3-(3-氟-4-羟基苯基)-6-甲氧基香豆素的7-羟基化(70%)、3-(4-三氟甲氧基苯基)-6-甲氧基香豆素的7-羟基化(78%)、3-(3-甲氧基苯基)香豆素的7-羟基化(81%)以及戊氧基试卤灵O-脱戊基化(66%)的蛋白质标准化CYP探针活性显著降低。与对照组相比,WD组中3-(4-甲基苯基)-7-羟基香豆素的磺化(289%)和胞质儿茶酚O-甲基转移酶(COMT,148%)的活性显著增加。总之,WD诱导的雄性LDLrApoB小鼠脂肪变性与CYP氧化反应降低有关,但对葡萄糖醛酸化、磺化和胞质儿茶酚O-甲基化的结合反应没有明显影响。因此,与更健康的低脂饮食相比,WD可能会降低药物的代谢消除。