Setoguchi T, Salen G, Tint G S, Mosbach E H
J Clin Invest. 1974 May;53(5):1393-401. doi: 10.1172/JCI107688.
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.
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。