Department of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, 308 Harvard ST SE, 7-115C WDH Minneapolis, MN, USA.
Br J Clin Pharmacol. 2011 Jul;72(1):109-15. doi: 10.1111/j.1365-2125.2011.03959.x.
It is well established that oxidative and conjugative enzyme activity differs between obese and healthy-weight adults. However, the effect of obesity on drug metabolism in children has not been studied extensively. This study examined whether obese and healthy-weight children vary with respect to oxidative enzyme activity of CYP1A2, xanthine oxidase (XO) and conjugative enzyme activity of N-acetyltransferase 2 (NAT2).
In vivo CYP1A2, XO and NAT2 activity was assessed in obese (n= 9) and lean (n= 16) children between the ages of 6-10 years using caffeine (118.3 ml Coca Cola®) as probe. Urine samples were collected in 2-h increments over 8 h. Caffeine and metabolites were measured using LC/MS, and urinary metabolic ratios were determined based on reported methods.
Sixteen healthy-weight and nine obese children were evaluated. XO activity was elevated in paediatric obese volunteers compared with non-obese paediatric volunteers (XO metabolic ratio of 0.7 ± 0.06 vs. 0.6 ± 0.06, respectively, 95% CI 0.046, 0.154, P < 0.001). NAT2 activity was fivefold higher in the obese (1 ± 0.4) as compared with non-obese children (0.2 ± 0.1), 95% CI 0.26, 1.34, P < 0.05. However, no difference was observed in CYP1A2 activity between the groups (95% CI -2.72, 0.12, P > 0.05).
This study provides evidence that obese children have elevated XO and NAT2 enzyme activity when compared with healthy-weight controls. Further studies are needed to determine how this may impact the efficacy of therapeutic agents that may undergo metabolism by these enzymes.
已有研究证实,肥胖人群和健康体重人群的氧化酶和结合酶活性存在差异。然而,肥胖对儿童药物代谢的影响尚未得到广泛研究。本研究旨在探讨肥胖儿童和健康体重儿童的细胞色素 P4501A2(CYP1A2)、黄嘌呤氧化酶(XO)的氧化酶活性和 N-乙酰基转移酶 2(NAT2)的结合酶活性是否存在差异。
本研究采用 LC/MS 法检测咖啡因(118.3ml 可口可乐®)作为探针的体内 CYP1A2、XO 和 NAT2 活性,对 6-10 岁的肥胖儿童(n=9)和瘦儿童(n=16)进行了研究。在 8 小时内每 2 小时采集一次尿液样本。根据报道的方法,测定咖啡因及其代谢产物,并基于代谢比值确定尿液代谢比值。
共评估了 16 名健康体重儿童和 9 名肥胖儿童。与非肥胖儿科志愿者相比,肥胖儿科志愿者的 XO 活性升高(XO 代谢比为 0.7±0.06 比 0.6±0.06,95%CI 0.046,0.154,P<0.001)。肥胖儿童的 NAT2 活性是正常体重儿童的五倍(1±0.4 比 0.2±0.1,95%CI 0.26,1.34,P<0.05)。然而,两组 CYP1A2 活性无差异(95%CI-2.72,0.12,P>0.05)。
本研究提供了证据表明,与健康体重对照组相比,肥胖儿童的 XO 和 NAT2 酶活性升高。需要进一步研究以确定这可能如何影响可能通过这些酶代谢的治疗药物的疗效。