Department of Clinical Chemistry and Pediatrics, Laboratory Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, The Netherlands.
Department of Clinical Chemistry and Pediatrics, Laboratory Genetic Metabolic Diseases, Academic Medical Center, Amsterdam, The Netherlands.
Mol Aspects Med. 2017 Aug;56:10-24. doi: 10.1016/j.mam.2017.03.003. Epub 2017 Mar 22.
Bile acids facilitate the absorption of lipids in the gut, but are also needed to maintain cholesterol homeostasis, induce bile flow, excrete toxic substances and regulate energy metabolism by acting as signaling molecules. Bile acid biosynthesis is a complex process distributed across many cellular organelles and requires at least 17 enzymes in addition to different metabolite transport proteins to synthesize the two primary bile acids, cholic acid and chenodeoxycholic acid. Disorders of bile acid synthesis can present from the neonatal period to adulthood and have very diverse clinical symptoms ranging from cholestatic liver disease to neuropsychiatric symptoms and spastic paraplegias. This review describes the different bile acid synthesis pathways followed by a summary of the current knowledge on hereditary disorders of human bile acid biosynthesis with a special focus on diagnostic bile acid profiling using mass spectrometry.
胆汁酸有助于肠道内脂质的吸收,但也需要维持胆固醇的体内平衡、诱导胆汁流动、排泄有毒物质,并通过充当信号分子来调节能量代谢。胆汁酸的生物合成是一个复杂的过程,分布在许多细胞细胞器中,除了不同的代谢物转运蛋白外,还需要至少 17 种酶来合成两种主要的胆汁酸,即胆酸和鹅脱氧胆酸。胆汁酸合成的紊乱可从新生儿期到成年期出现,临床表现非常多样化,从胆汁淤积性肝病到神经精神症状和痉挛性截瘫都有。这篇综述描述了不同的胆汁酸合成途径,然后总结了目前关于人类胆汁酸生物合成遗传紊乱的知识,特别关注使用质谱法进行诊断性胆汁酸分析。