Hanson R F, Szczepanik-VanLeeuwen P, Williams G C, Grabowski G, Sharp H L
Science. 1979 Mar 16;203(4385):1107-8. doi: 10.1126/science.424737.
Abnormal mitochondrial structure and function have been documented in patients with Zellweger's syndrome (cerebrohepatorenal syndrome). In vitro studies have suggested that the formation of C24 bile acids (chenodeoxycholic acid and cholic acid) from C27 cholesterol requires mitochondrial oxidative clevage of the terminal three carbons of the side chain. Therefore, three patients with Zellweger's syndrome were examined for the presence of mitochondrial defects in bile acid synthesis. All three excreted excessive amounts of 3 alpha, 7 alpha-dihydroxy-5 beta-cholestan-26-oicacid, 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestan-26-oic acid, and 3 alpha, 7 alpha, 12 alpha, 24 xi-tetrahydroxy-5 beta-cholestan-26-oic acid (varanic acid), precursors of chenodeoxycholic acid and cholic acid that have undergone only partial side chain oxidation. These findings give added support to the role of mitochondrial oxidative side chain cleavage in the overall scheme of bile acid synthesis.
在齐-韦氏综合征(脑肝肾综合征)患者中,已证实存在线粒体结构和功能异常。体外研究表明,由C27胆固醇生成C24胆汁酸(鹅去氧胆酸和胆酸)需要线粒体对侧链末端三个碳原子进行氧化裂解。因此,对三名齐-韦氏综合征患者进行了检查,以确定胆汁酸合成中是否存在线粒体缺陷。所有三名患者都排泄出过量的3α,7α-二羟基-5β-胆甾烷-26-酸、3α,7α,12α-三羟基-5β-胆甾烷-26-酸和3α,7α,12α,24ξ-四羟基-5β-胆甾烷-26-酸(瓦拉尼酸),这些是仅经历了部分侧链氧化的鹅去氧胆酸和胆酸的前体。这些发现进一步支持了线粒体氧化侧链裂解在胆汁酸合成总体过程中的作用。