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1
A biochemical abnormality in cerebrotendinous xanthomatosis. Impairment of bile acid biosynthesis associated with incomplete degradation of the cholesterol side chain.脑腱黄瘤病中的一种生化异常。胆汁酸生物合成受损,与胆固醇侧链不完全降解相关。
J Clin Invest. 1974 May;53(5):1393-401. doi: 10.1172/JCI107688.
2
Cholic acid biosynthesis: the enzymatic defect in cerebrotendinous xanthomatosis.胆酸生物合成:脑腱黄瘤病中的酶缺陷
J Clin Invest. 1979 Jan;63(1):38-44. doi: 10.1172/JCI109275.
3
Identification of pentahydroxy bile alcohols in cerebrotendinous xanthomatosis: characterization of 5beta-cholestane-3alpha, 7alpha, 12alpha, 24xi, 25-pentol and 5beta-cholestane-3alpha, 7alpha, 12alpha, 23xi, 25-pentol.脑腱黄瘤病中五羟基胆汁醇的鉴定:5β-胆甾烷-3α, 7α, 12α, 24ξ, 25-戊醇和5β-胆甾烷-3α, 7α, 12α, 23ξ, 25-戊醇的表征
J Lipid Res. 1975 Jul;16(4):280-6.
4
Differences in hepatic levels of intermediates in bile acid biosynthesis between Cyp27(-/-) mice and CTX.Cyp27(-/-)小鼠与环磷酰胺处理小鼠之间胆汁酸生物合成中间产物肝脏水平的差异。
J Lipid Res. 2001 Feb;42(2):291-300.
5
Bile alcohol metabolism in man. Conversion of 5beta-cholestane-3alpha, 7alpha,12alpha, 25-tetrol to cholic acid.人体内胆汁醇的代谢。5β-胆甾烷-3α,7α,12α,25-四醇向胆酸的转化。
J Clin Invest. 1975 Jul;56(1):226-31. doi: 10.1172/JCI108071.
6
Side chain hydroxylations in bile acid biosynthesis catalyzed by CYP3A are markedly up-regulated in Cyp27-/- mice but not in cerebrotendinous xanthomatosis.由CYP3A催化的胆汁酸生物合成中的侧链羟基化在Cyp27基因敲除小鼠中显著上调,但在脑腱性黄瘤病中未上调。
J Biol Chem. 2001 Sep 14;276(37):34579-85. doi: 10.1074/jbc.M103025200. Epub 2001 Jul 13.
7
Metabolism of bile alcohols in the perfused rabbit liver.灌注兔肝脏中胆汁醇的代谢
J Biol Chem. 1976 May 10;251(9):2709-15.
8
A 25-hydroxylation pathway of cholic acid biosynthesis in man and rat.人和大鼠体内胆酸生物合成的25-羟化途径。
J Clin Invest. 1976 Apr;57(4):897-903. doi: 10.1172/JCI108366.
9
Biosynthesis of bile acids in cerebrotendinous xanthomatosis. Relationship of bile acid pool sizes and synthesis rates to hydroxylations at C-12, C-25, and C-26.脑腱黄瘤病中胆汁酸的生物合成。胆汁酸池大小和合成速率与C-12、C-25和C-26位羟基化的关系。
J Clin Invest. 1985 Aug;76(2):744-51. doi: 10.1172/JCI112030.
10
Metabolism of potential precursors of chenodeoxycholic acid in cerebrotendinous xanthomatosis (CTX).脑腱黄瘤病(CTX)中鹅去氧胆酸潜在前体的代谢
J Lipid Res. 1979 Jan;20(1):22-30.

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Cerebrotendinous xanthomatosis.
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Cerebrotendinous xanthomatosis: a comprehensive review of pathogenesis, clinical manifestations, diagnosis, and management.脑腱黄瘤病:发病机制、临床表现、诊断及治疗的全面综述
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Disorders of bile acid synthesis.胆汁酸合成障碍。
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8
A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis.一位常染色体隐性遗传脑腱黄瘤病女性患者的固醇 27-羟化酶基因的新突变。
Orphanet J Rare Dis. 2010 Oct 6;5:27. doi: 10.1186/1750-1172-5-27.
9
Anomalous enantioselectivity in the sharpless asymmetric dihydroxylation reaction of 24-nor-5beta-cholest-23-ene-3alpha,7alpha,12alpha-triol: synthesis of substrates for studies of cholesterol side-chain oxidation.24-降-5β-胆甾-23-烯-3α,7α,12α-三醇的夏普莱斯不对称双羟基化反应中的异常对映选择性:用于胆固醇侧链氧化研究的底物合成
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10
Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease.胆汁酸合成中一种新的先天性代谢缺陷的鉴定:氧化甾醇7α-羟化酶基因突变导致严重的新生儿肝病。
J Clin Invest. 1998 Nov 1;102(9):1690-703. doi: 10.1172/JCI2962.

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Stero-bile acids and bile sterols. 47. Syntheses of 3alpha,7alpha,12alpha,25,26- and 3alpha,7alpha,12alpha,24,25-pentahydroxycoprostanes.甾体胆汁酸和胆汁甾醇。47. 3α,7α,12α,25,26-和3α,7α,12α,24,25-五羟基粪甾烷的合成。
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Catabolism in vitro of cholesterol. III. Oxidation of 3 alpha, 7 alpha, 12 alpha-trihydroxy-coprostane, 3 alpha, 7 alpha, 12 alpha-trihydroxy-24-ketocoprostane, and 3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxycoprostane by rat liver mitochondria.
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Mass spectrometry in structural and stereochemical problems. CXXV. Mass spectrometry of some steroid trimethylsilyl ethers.
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Stero-bile acids and bile alcohols. 93. Metabolism of 5-beta-cholestane-3-alpha, 7-alpha, 12-alpha, 25-tetrol.甾体胆汁酸和胆汁醇。93. 5-β-胆甾烷-3-α,7-α,12-α,25-四醇的代谢
Hiroshima J Med Sci. 1966 Dec;15(4):375-90.
5
Measurements of cholesterol turnover, synthesis, and absorption in man, carried out by isotope kinetic and sterol balance methods.采用同位素动力学和甾醇平衡方法对人体胆固醇周转、合成及吸收进行的测量。
J Lipid Res. 1969 Jan;10(1):91-107.
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25-hydroxyergocalciferol: a biologically active metabolite of vitamin D2.
Biochem Biophys Res Commun. 1969 Apr 29;35(2):182-5. doi: 10.1016/0006-291x(69)90264-2.
7
Cholestanol deposition in cerebrotendinous xanthomatosis. A possible mechanism.脑腱性黄瘤病中的胆甾烷醇沉积。一种可能的机制。
Ann Intern Med. 1971 Dec;75(6):843-51. doi: 10.7326/0003-4819-75-6-843.
8
Determination of hepatic 3-hydroxy-3-methylglutaryl CoA reductase activity in man.
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9
Improved estimation of body masses and turnover of cholesterol by computerized input--output analysis.通过计算机化投入产出分析改进对体重和胆固醇周转率的估计。
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Three-pool model of the long-term turnover of plasma cholesterol in man.人体血浆胆固醇长期周转的三池模型。
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脑腱黄瘤病中的一种生化异常。胆汁酸生物合成受损,与胆固醇侧链不完全降解相关。

A biochemical abnormality in cerebrotendinous xanthomatosis. Impairment of bile acid biosynthesis associated with incomplete degradation of the cholesterol side chain.

作者信息

Setoguchi T, Salen G, Tint G S, Mosbach E H

出版信息

J Clin Invest. 1974 May;53(5):1393-401. doi: 10.1172/JCI107688.

DOI:10.1172/JCI107688
PMID:4825231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC302628/
Abstract

Bile acid production in cerebrotendinous xanthomatosis (CTX) is subnormal, yet the activity of cholesterol 7alpha-hydroxylase, the rate-determining enzyme of bile acid synthesis, is elevated. To explain this discrepancy, bile acid precursors were sought in bile and feces of three CTX subjects. Over 10% of the total sterols excreted in bile and feces consisted of compounds more polar than cholesterol. Chromatographic analysis of the polar fractions in conjunction with gasliquid chromatography (GLC)-mass spectrometry indicated two major constituents, 5beta-cholestane-3alpha,7alpha,12alpha,25-tetrol and 5beta-cholestane-3alpha,7alpha,12alpha,24xi,25-pentol. After i.v. injection of [4-(14)C]cholesterol both bile alcohols were radioactive proving that they were derived from cholesterol. The accumulation of alcohols hydroxylated at C-25 and C-24,25 suggests that decreased bile acid synthesis in CTX results from impaired oxidation of the cholesterol side chain. This finding and the virtual absence of intermediates hydroxylated at C-26 indicate that current views of the major pathway of bile acid synthesis may require revision.

摘要

脑腱黄瘤病(CTX)中胆汁酸的生成低于正常水平,然而胆汁酸合成的限速酶胆固醇7α-羟化酶的活性却升高。为了解释这种差异,在三名CTX患者的胆汁和粪便中寻找胆汁酸前体。胆汁和粪便中排泄的总固醇中超过10%由比胆固醇极性更强的化合物组成。对极性部分进行色谱分析并结合气液色谱(GLC)-质谱分析表明有两种主要成分,5β-胆甾烷-3α,7α,12α,25-四醇和5β-胆甾烷-3α,7α,12α,24ξ,25-五醇。静脉注射[4-(14)C]胆固醇后,两种胆汁醇都具有放射性,证明它们源自胆固醇。C-25和C-24,25位羟基化醇的积累表明,CTX中胆汁酸合成减少是由于胆固醇侧链氧化受损所致。这一发现以及几乎不存在C-26位羟基化的中间体表明,目前关于胆汁酸合成主要途径的观点可能需要修正。