Quantitative Pharmacology DMPK Department, UCB BioPharma, Chemin du Foriest, 1420, Braine L'Alleud, Belgium.
Research Division of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
AAPS J. 2019 May 28;21(4):67. doi: 10.1208/s12248-019-0340-z.
Available data on human brain P-glycoprotein ontogeny during infancy and childhood are limited. This review discusses the current body of data relating to maturation of human brain P-glycoprotein including transporter expression levels in post-mortem human brain samples, in vivo transporter activity using probe substrates, surrogate marker endpoints, and extrapolations from animal models. Overall, the data tend to confirm that human brain P-glycoprotein activity keeps developing after birth, although with a developmental time frame that remains unclear. This knowledge gap is a concern given the critical role of brain P-glycoprotein in drug safety and efficacy, and the vulnerable nature of the pediatric population. Future research could include the measurement of brain P-glycoprotein activity across age groups using positron emission tomography or central pharmacodynamic responses. For now, caution is advised when extrapolating adult data to children aged younger than 2 years for drugs with P-glycoprotein-dependent central nervous system activity.
关于婴儿期和儿童期人脑 P-糖蛋白发生的可用数据有限。本综述讨论了目前与人类大脑 P-糖蛋白成熟相关的数据,包括死后人脑样本中的转运蛋白表达水平、使用探针底物的体内转运蛋白活性、替代标志物终点以及来自动物模型的推断。总的来说,这些数据证实了人类大脑 P-糖蛋白的活性在出生后仍在继续发展,尽管其发育时间框架尚不清楚。鉴于大脑 P-糖蛋白在药物安全性和疗效方面的关键作用,以及儿科人群的脆弱性,这一知识空白令人担忧。未来的研究可以包括使用正电子发射断层扫描或中枢药效反应来测量不同年龄段的大脑 P-糖蛋白活性。目前,对于具有 P-糖蛋白依赖性中枢神经系统活性的药物,当将成人数据外推至 2 岁以下儿童时,应谨慎行事。