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P-glycoprotein in the Developing Human Brain: A Review of the Effects of Ontogeny on the Safety of Opioids in Neonates

机译:人脑发育中的P-糖蛋白:个体发育对新生儿阿片类药物安全性的影响的综述

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摘要

The human blood brain barrier is responsible for maintaining brain homeostasis and protecting against potentially toxic substances. The ATP-binding cassette drug efflux protein, P-glycoprotein (P-gp) is a key player in actively extruding a wide range of xenobiotics such as opioids from the brain. Because the blood brain barrier is structurally and functionally immature in neonates, opioids may have a greater penetration to the central nervous system. This may influence the efficacy and safety of opioids in the newborn. Understanding the extent of P-gp's expression in the brain in the embryo, fetus, and newborn will facilitate rational opioid use during pregnancy and the neonatal period. This review aims to summarize the current evidence that associates the ontogeny of P-gp and the susceptibility to opioid-induced adverse respiratory effects in neonates. To date, evidence suggests that the expression of P-gp in the human brain is low at birth, contributing to increased susceptibility.
机译:人血脑屏障负责维持脑稳态并防止潜在的有毒物质。 ATP结合盒式药物外排蛋白P-糖蛋白(P-gp)是主动从大脑中挤出各种异质生物(如阿片类药物)的关键因素。由于新生儿的血脑屏障在结构和功能上尚不成熟,因此阿片类药物可能会更多地渗透到中枢神经系统。这可能会影响新生儿阿片类药物的疗效和安全性。了解P-gp在胚胎,胎儿和新生儿的大脑中的表达程度将有助于在怀孕和新生儿期合理使用阿片类药物。这篇综述旨在总结当前证据,这些证据将P-gp的个体发育与新生儿对阿片类药物引起的不良呼吸作用的敏感性相关联。迄今为止,有证据表明,人脑中P-gp的表达在出生时就很低,导致易感性增加。

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