Hepatic function and physiology in the newborn

S.V Beath
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引用次数: 97

Abstract

The liver develops from progenitor cells into a well-differentiated organ in which bile secretion can be observed by 12 weeks' gestation. Full maturity takes up to two years after birth to be achieved, and involves the normal expression of signalling pathways such as that responsible for the JAG1 genes (aberrations occur in Alagille's syndrome), amino acid transport and insulin growth factors. At birth, hepatocytes are already specialized and have two surfaces: the sinusoidal side receives and absorbs a mixture of oxygenated blood and nutrients from the portal vein; the other surface delivers bile and other products of conjugation and metabolism (including drugs) to the canalicular network which joins up to the bile ductules. There is a rapid induction of functions such as transamination, glutamyl transferase, synthesis of coagulation factors, bile production and transport as soon as the umbilical supply is interrupted.

Anatomical specialization can be observed across the hepatic acinus which has three distinct zones. Zone 1 borders the portal tracts (also known as periportal hepatocytes) and is noted for hepatocyte regeneration, bile duct proliferation and gluconeogenesis. Zone 3 borders the central vein and is associated with detoxification (e.g. paracetamol), aerobic metabolism, glycolysis and hydrolysis and zone 2 is an area of mixed function between the two zones.

Preterm infants are at special risk of hepatic decompensation because their immaturity results in a delay in achieving normal detoxifying and synthetic function. Hypoxia and sepsis are also frequent and serious causes of liver dysfunction in neonates.

Stem cell research has produced many answers to the questions about liver development and regeneration, and genetic studies including studies of susceptibility genes may yield further insights. The possibility that fatty liver (increasingly recognized as non-alcoholic steatohepatitis or NASH) may have roots in the neonatal period is a concept which may have important long-term implications.

新生儿肝功能与生理
肝脏由祖细胞发育为分化良好的器官,在妊娠12周时可观察到胆汁分泌。完全成熟需要在出生后两年才能实现,这涉及到信号通路的正常表达,比如负责JAG1基因的信号通路(畸变发生在阿拉吉尔综合征中)、氨基酸运输和胰岛素生长因子。出生时,肝细胞已经特化,有两个表面:窦侧接收和吸收来自门静脉的含氧血液和营养物质的混合物;另一个表面将胆汁和其他结合和代谢产物(包括药物)输送到连接到胆管的小管网络。一旦脐带供应中断,转氨酶、谷氨酰转移酶、凝血因子的合成、胆汁的产生和运输等功能就会迅速诱导。解剖专门化可以观察到横跨肝腺泡,它有三个不同的区域。1区毗邻门静脉束(也称为门静脉周围肝细胞),以肝细胞再生、胆管增殖和糖异生而闻名。3区毗邻中央静脉,与解毒(如扑热息痛)、有氧代谢、糖酵解和水解有关,2区是两个区域之间的混合功能区域。早产儿有肝脏失代偿的特殊风险,因为他们的不成熟导致实现正常解毒和合成功能的延迟。缺氧和脓毒症也是新生儿肝功能障碍的常见和严重原因。干细胞研究已经为肝脏发育和再生问题提供了许多答案,而包括易感基因在内的遗传研究可能会产生进一步的见解。脂肪肝(越来越多地被认为是非酒精性脂肪性肝炎或NASH)可能起源于新生儿期,这一概念可能具有重要的长期意义。
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