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UGT1A6 和 UGT2B15 多态性与乙酰氨基酚结合反应对随机对照选择水果和蔬菜饮食的影响。

UGT1A6 and UGT2B15 polymorphisms and acetaminophen conjugation in response to a randomized, controlled diet of select fruits and vegetables.

机构信息

Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N, Seattle, WA 98109, USA.

出版信息

Drug Metab Dispos. 2011 Sep;39(9):1650-7. doi: 10.1124/dmd.111.039149. Epub 2011 Jun 10.

Abstract

Acetaminophen (APAP) glucuronidation is thought to occur mainly by UDP-glucuronosyltransferases (UGT) in the UGT1A family. Interindividual variation in APAP glucuronidation is attributed in part to polymorphisms in UGT1As. However, evidence suggests that UGT2B15 may also be important. We evaluated, in a controlled feeding trial, whether APAP conjugation differed by UGT1A6 and UGT2B15 genotypes and whether supplementation of known dietary inducers of UGT (crucifers, soy, and citrus) modulated APAP glucuronidation compared with a diet devoid of fruits and vegetables (F&V). Healthy adults (n = 66) received 1000 mg of APAP orally on days 7 and 14 of each 2-week feeding period and collected saliva and urine over 12 h. Urinary recovery of the percentage of the APAP dose as free APAP was higher (P = 0.02), and the percentage as APAP glucuronide (APAPG) was lower (P = 0.004) in women. The percentage of APAP was higher among UGT1A6*1/*1 genotypes, relative to *1/*2 and *2/*2 genotypes (P = 0.045). For UGT2B15, the percentage of APAPG decreased (P < 0.0001) and that of APAP sulfate increased (P = 0.002) in an allelic dose-dependent manner across genotypes from *1/*1 to *2/*2. There was a significant diet × UGT2B15 genotype interaction for the APAPG ratio (APAPG/total metabolites × 100) (P = 0.03), with *1/*1 genotypes having an approximately 2-fold higher F&V to basal diet difference in response compared with *1/*2 and 2/2 genotypes. Salivary APAP maximum concentration (C(max)) was significantly higher in women (P = 0.0003), with F&V (P = 0.003), and among UGT1A62/2 and UGT2B151/2 genotypes (P = 0.02 and 0.002, respectively). APAP half-life was longer in UGT2B152/2 genotypes with F&V (P = 0.009). APAP glucuronidation was significantly influenced by the UGT2B152 polymorphism, supporting a role in vivo for UGT2B15 in APAP glucuronidation, whereas the contribution of UGT1A62 was modest. Selected F&V known to affect UGT activity led to greater glucuronidation and less sulfation.

摘要

对乙酰氨基酚(APAP)的葡萄糖醛酸化被认为主要发生在 UDP-葡糖醛酸基转移酶(UGT)家族的 UGT1A 中。APAP 葡萄糖醛酸化的个体间差异部分归因于 UGT1A 的多态性。然而,有证据表明 UGT2B15 也可能很重要。我们在一项对照喂养试验中评估了 UGT1A6 和 UGT2B15 基因型是否会导致 APAP 结合的差异,以及已知的 UGT(十字花科植物、大豆和柑橘类)膳食诱导物是否会与不含水果和蔬菜(F&V)的饮食相比调节 APAP 葡萄糖醛酸化。健康成年人(n = 66)在每个为期两周的喂养期的第 7 天和第 14 天口服 1000 毫克 APAP,并在 12 小时内收集唾液和尿液。尿液中游离 APAP 占 APAP 剂量的百分比较高(P = 0.02),APAP 葡萄糖醛酸酯(APAPG)的百分比较低(P = 0.004)在女性中。与 UGT1A6*1/2 和2/2 基因型相比,UGT1A61/1 基因型的 APAP 百分比更高(P = 0.045)。对于 UGT2B15,APAPG 的百分比随着基因型从1/1 到2/2 的等位基因剂量依赖性降低(P < 0.0001),而 APAP 硫酸盐的百分比增加(P = 0.002)。APAPG/总代谢物的比值(APAPG/总代谢物×100)(P = 0.03)存在显著的饮食×UGT2B15 基因型相互作用,与1/2 和2/*2 基因型相比,1/1 基因型对 F&V 到基础饮食的差异的反应约高 2 倍。女性的唾液 APAP 最大浓度(C(max))显著较高(P = 0.0003),F&V(P = 0.003),UGT1A62/2 和 UGT2B151/2 基因型(P = 0.02 和 0.002,分别)。UGT2B152/2 基因型与 F&V 同时存在时,APAP 的半衰期更长(P = 0.009)。APAP 葡萄糖醛酸化明显受 UGT2B152 多态性的影响,支持 UGT2B15 在体内对 APAP 葡萄糖醛酸化的作用,而 UGT1A62 的作用则较为温和。已知影响 UGT 活性的选定 F&V 导致更大的葡萄糖醛酸化和更少的硫酸盐化。

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