Excretion of 3β‐hydroxy‐5‐cholenoic and 3a‐hydroxy‐5a‐cholanoic acids in urine of infants with biliary atresia
Excretion of 3β‐hydroxy‐5‐cholenoic and 3a‐hydroxy‐5a‐cholanoic acids in urine of infants with biliary atresia
复制标题
胆道闭锁婴儿尿液中 3β-羟基-5-胆烯酸和 3a-羟基-5a-胆烷酸的排泄
DOI:
10.1016/0014-5793(71)80047-9
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发表时间:
1971
期刊:
影响因子:
3.5
通讯作者:
B. Strandvik
中科院分区:
文献类型:
--
作者:
I. Makino;Jan Sjövall;A. Norman;B. Strandvik
Infants with extrahepatic bile duct atresia have no enterohepatic circulation of bile acids. Conjugates of cholic (3a, 7a, 12a-trihydroxy-S&cholanoic) and chenodeoxycholic (3q ircr-dihydroxy-SP-cholanoic) acids are the main bile acids excreted in urine [l]. In addition, several compounds with chromatographic properties of mono-and dihydroxycholanoic acids have been detected [l]. This paper reports the identification of 3/I-hydroxy-5-cholenoic and 3cu-hydroxy-So-cholanoic (allolithocholic) acids and S-cholestene-3/3, 24&+ diol as the major components among the less polar compounds isolated by aluminum oxide chromatography. These compounds contained little or no radioactivity in samples from a patient given 4-14C-cholesterol. The results indicate that 3/I-hydroxy-5 cholenoic acid is formed in considerable amounts in infants with biliary atresia, and that the major part is not formed from the cholesterol pool used in the synthesis of cholic and chenodeoxycholic acids.