Manchester Pharmacy School (B.A., M.R.R., J.B., A.R-H.), University of Manchester, Manchester, United Kingdom; Simcyp Limited (A.R-H.), a Certara Company, Sheffield, United Kingdom.
Drug Metab Dispos. 2014 Apr;42(4):500-10. doi: 10.1124/dmd.113.055632. Epub 2014 Jan 9.
Cytochrome P450 (P450) and uridine 5'-diphospho-glucuronosyltransferase (UGT) enzymes mediate a major proportion of phase I and phase II metabolism of xenobiotics. In vitro-in vivo extrapolation (IVIVE) of hepatic clearance in conjunction with physiologically-based pharmacokinetics (PBPK) has become common practice in drug development. However, prediction of xenobiotic kinetics in virtual populations requires knowledge of both enzyme abundances and the extent to which these correlate. A multiplexed quantification concatemer (QconCAT) strategy was used in this study to quantify the expression of several P450 and UGT enzymes simultaneously and to establish correlations between various enzyme abundances in 24 individual liver samples (ages 27-66, 14 male). Abundances were comparable to previously reported values, including CYP2C9 (40.0 ± 26.0 pmol mg(-1)), CYP2D6 (11.9 ± 13.2 pmol mg(-1)), CYP3A4 (68.1 ± 52.3 pmol mg(-1)), UGT1A1 (33.6 ± 34.0 pmol mg(-1)), and UGT2B7 (82.9 ± 36.1 pmol mg(-1)), expressed as mean ± S.D. Previous reports of correlations in expression of various P450 (CYP3A4/CYP3A5*1/*3, CYP2C8/CYP2C9, and CYP3A4/CYP2B6) were confirmed. New correlations were demonstrated between UGTs [including UGT1A6/UGT1A9 (r(s) = 0.82, P < 0.0001) and UGT2B4/UGT2B15 (r(s) = 0.71, P < 0.0001)]. Expression of some P450 and UGT enzymes were shown to be correlated [including CYP1A2/UGT2B4 (r(s) = 0.67, P = 0.0002)]. The expression of CYP3A5 in individuals with *1/*3 genotype (n = 11) was higher than those with *3/*3 genotype (n = 10) (P < 0.0001). No significant effect of gender or history of smoking or alcohol use on enzyme expression was observed; however, expression of several enzymes declined with age. The correlation matrix produced for the first time by this study can be used to generate more realistic virtual populations with respect to abundance of various enzymes.
细胞色素 P450(P450)和尿苷 5'-二磷酸葡萄糖醛酸基转移酶(UGT)酶介导了外源性物质的主要 I 相和 II 相代谢。体外-体内外推(IVIVE)与基于生理学的药代动力学(PBPK)相结合,已成为药物开发中的常见做法。然而,预测虚拟人群中外源性物质的动力学需要了解酶丰度以及这些丰度之间的相关性。本研究采用多重定量串联(QconCAT)策略,同时定量检测 24 个个体肝样本(年龄 27-66 岁,男性 14 名)中几种 P450 和 UGT 酶的表达,并建立各种酶丰度之间的相关性。丰度与以前报道的值相当,包括 CYP2C9(40.0±26.0 pmol mg-1)、CYP2D6(11.9±13.2 pmol mg-1)、CYP3A4(68.1±52.3 pmol mg-1)、UGT1A1(33.6±34.0 pmol mg-1)和 UGT2B7(82.9±36.1 pmol mg-1),表示为平均值±S.D. 先前报道的各种 P450(CYP3A4/CYP3A5*1/3、CYP2C8/CYP2C9 和 CYP3A4/CYP2B6)表达的相关性得到了证实。还证实了 UGT 之间的新相关性[包括 UGT1A6/UGT1A9(r(s)=0.82,P<0.0001)和 UGT2B4/UGT2B15(r(s)=0.71,P<0.0001)]。一些 P450 和 UGT 酶的表达显示出相关性[包括 CYP1A2/UGT2B4(r(s)=0.67,P=0.0002)]。具有1/3 基因型(n=11)的个体中 CYP3A5 的表达高于具有3/*3 基因型(n=10)的个体(P<0.0001)。未观察到性别、吸烟或饮酒史对酶表达有显著影响;然而,几种酶的表达随年龄增长而下降。本研究首次生成的相关矩阵可用于生成更符合各种酶丰度的真实虚拟人群。