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1
Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.在齐-韦二氏脑肝肾综合征中,过氧化物酶体对C27-甾体侧链的切割存在缺陷。
J Clin Invest. 1985 Feb;75(2):427-35. doi: 10.1172/JCI111717.
2
In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.关于齐-韦二氏综合征患者胆汁酸形成的体内和体外研究。过氧化物酶体在胆酸和鹅去氧胆酸正常生物合成中起重要作用的证据。
J Clin Invest. 1985 Dec;76(6):2393-402. doi: 10.1172/JCI112252.
3
Role of peroxisomes in the biosynthesis of bile acids.过氧化物酶体在胆汁酸生物合成中的作用。
Scand J Clin Lab Invest Suppl. 1985;177:23-31.
4
Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome.过氧化物酶体在人肝脏中鹅去氧胆酸形成中的重要性。齐-韦综合征中3α,7α-二羟基-5β-胆甾烷酸的代谢。
Pediatr Res. 1991 Jan;29(1):64-9. doi: 10.1203/00006450-199101000-00013.
5
Bile acids and bile alcohols in two patients with Zellweger (cerebro-hepato-renal) syndrome.两名患有泽尔韦格(脑肝肾)综合征患者的胆汁酸和胆汁醇
J Pediatr Gastroenterol Nutr. 1986 Sep-Oct;5(5):701-10. doi: 10.1097/00005176-198609000-00006.
6
Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.过氧化物酶体3-氧代酰基辅酶A硫解酶缺乏症中的胆汁酸谱
J Clin Invest. 1990 Apr;85(4):1267-73. doi: 10.1172/JCI114563.
7
Biosynthesis of bile acids in man. An in vivo evaluation of the conversion of R and S 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic and 3 alpha, 7 alpha, 12 alpha-24 xi-tetrahydroxy-5 beta-cholestanoic acids to cholic acid.
J Biol Chem. 1981 Jan 25;256(2):912-6.
8
Human hepatoblastoma cells (HepG2) and rat hepatoma cells are defective in important enzyme activities in the oxidation of the C27 steroid side chain in bile acid formation.人肝癌细胞(HepG2)和大鼠肝癌细胞在胆汁酸形成过程中C27甾体侧链氧化的重要酶活性方面存在缺陷。
J Lipid Res. 1993 Dec;34(12):2041-50.
9
Configuration of the 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholest-24-enoic acid, an intermediate in the peroxisomal conversion of 3 alpha,7 alpha,12-trihydroxy-5 beta-cholestanoic acid to cholic acid in rat liver.
Biochem Int. 1992 Mar;26(4):725-30.
10
Zellweger's cerebro-hepato-renal syndrome--variations in expressivity and in defects of bile acid synthesis.
Clin Genet. 1983 Nov;24(5):313-9.

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1
Two Major Bile Acids in the Hornbills, (24R,25S)-3α,7α,24-Trihydroxy-5β-cholestan-27-oyl Taurine and Its 12α-Hydroxy Derivative.犀鸟体内的两种主要胆汁酸,(24R,25S)-3α,7α,24-三羟基-5β-胆甾烷-27-酰牛磺酸及其12α-羟基衍生物。
Lipids. 2016 Jun;51(6):757-68. doi: 10.1007/s11745-016-4150-0. Epub 2016 Apr 23.
2
Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders.过氧化物酶体缺乏症患者中白三烯降解受损。
J Clin Invest. 1993 Mar;91(3):881-8. doi: 10.1172/JCI116309.
3
Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.过氧化物酶体酰基辅酶A氧化酶缺乏症和双功能酶缺乏症的新型亚型,伴有可检测到的酶蛋白:通过互补分析进行鉴定。
Am J Hum Genet. 1994 Jan;54(1):36-43.
4
In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.关于齐-韦二氏综合征患者胆汁酸形成的体内和体外研究。过氧化物酶体在胆酸和鹅去氧胆酸正常生物合成中起重要作用的证据。
J Clin Invest. 1985 Dec;76(6):2393-402. doi: 10.1172/JCI112252.
5
Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).在缺乏可识别过氧化物酶体的人(齐-韦综合征)的肝脏中存在过氧化物酶体22-kDa整合膜蛋白。
Proc Natl Acad Sci U S A. 1986 Dec;83(23):9193-6. doi: 10.1073/pnas.83.23.9193.
6
Peroxisomal disorders: a newly recognised group of genetic diseases.过氧化物酶体病:一组新发现的遗传性疾病。
Eur J Pediatr. 1986 Feb;144(5):430-40. doi: 10.1007/BF00441734.
7
Subcellular localization of sterol carrier protein-2 in rat hepatocytes: its primary localization to peroxisomes.大鼠肝细胞中固醇载体蛋白-2的亚细胞定位:其主要定位于过氧化物酶体。
J Cell Biol. 1989 Apr;108(4):1353-61. doi: 10.1083/jcb.108.4.1353.
8
Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry.过氧化物酶体功能障碍综合征患者的血浆胆汁酸:毛细管气相色谱-质谱分析
Eur J Pediatr. 1987 Mar;146(2):166-73. doi: 10.1007/BF02343226.
9
Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.过氧化物酶体3-氧代酰基辅酶A硫解酶缺乏症中的胆汁酸谱
J Clin Invest. 1990 Apr;85(4):1267-73. doi: 10.1172/JCI114563.
10
The inborn errors of peroxisomal beta-oxidation: a review.过氧化物酶体β-氧化的先天性代谢缺陷:综述
J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330.

本文引用的文献

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A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS.一种多发性先天性缺陷的家族综合征。
Bull Johns Hopkins Hosp. 1964 Jun;114:402-14.
2
The turnover of cholic acid in man: bile acids and steroids.人体内胆酸的周转:胆汁酸与类固醇
Acta Physiol Scand. 1957 Sep 17;40(1):1-9. doi: 10.1111/j.1748-1716.1957.tb01473.x.
3
Conversion of 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid into cholic acid by rat liver peroxisomes.大鼠肝脏过氧化物酶体将3α,7α,12α-三羟基-5β-胆甾烷酸转化为胆酸。
FEBS Lett. 1980 Dec 1;121(2):345-8. doi: 10.1016/0014-5793(80)80377-2.
4
Liver in the cerebro-hepato-renal syndrome: defective bile acid synthesis and abnormal mitochondria.脑肝肾综合征中的肝脏:胆汁酸合成缺陷与线粒体异常
Gastroenterology. 1980 Dec;79(6):1311-7.
5
Cerebrotendinous xanthomatosis: a defect in mitochondrial 26-hydroxylation required for normal biosynthesis of cholic acid.脑腱黄瘤病:正常胆汁酸生物合成所需的线粒体26-羟化缺陷。
J Clin Invest. 1980 Jun;65(6):1418-30. doi: 10.1172/JCI109806.
6
An in vivo evaluation of the quantitative significance of several potential pathways to cholic and chenodeoxycholic acids from cholesterol in man.人体中胆固醇生成胆酸和鹅去氧胆酸的几种潜在途径的定量意义的体内评估。
J Lipid Res. 1980 May;21(4):455-66.
7
Biosynthesis of cholic acid in rat liver: formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy- and 3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxy-5 beta-cholestanoic acids.大鼠肝脏中胆酸的生物合成:由3α,7α,12α-三羟基-和3α,7α,12α,24-四羟基-5β-胆甾烷酸形成胆酸。
Lipids. 1980 Feb;15(2):113-21. doi: 10.1007/BF02533886.
8
Biosynthesis of bile acids in man. Multiple pathways to cholic acid and chenodeoxycholic acid.人体内胆汁酸的生物合成。胆酸和鹅脱氧胆酸的多种合成途径。
J Biol Chem. 1980 Apr 10;255(7):2925-33.
9
Cholic acid and chenodeoxycholic acid concentrations in serum during infancy and childhood.婴儿期和儿童期血清中胆酸和鹅去氧胆酸的浓度。
Acta Paediatr Scand. 1980 Sep;69(5):659-62. doi: 10.1111/j.1651-2227.1980.tb07339.x.
10
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.脑肝肾(泽尔韦格)综合征与新生儿肾上腺脑白质营养不良:表型及极长链脂肪酸蓄积方面的相似性
Johns Hopkins Med J. 1982 Dec;151(6):344-51.

在齐-韦二氏脑肝肾综合征中,过氧化物酶体对C27-甾体侧链的切割存在缺陷。

Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.

作者信息

Kase B F, Björkhem I, Hågå P, Pedersen J I

出版信息

J Clin Invest. 1985 Feb;75(2):427-35. doi: 10.1172/JCI111717.

DOI:10.1172/JCI111717
PMID:3973012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC423512/
Abstract

Based on in vitro work with rat liver, we recently suggested that the peroxisomal fraction is most important for the oxidation of 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid (THCA) into cholic acid. The cerebro-hepato-renal syndrome of Zellweger is a fatal recessive autosomal disorder, the most characteristic histological feature of which is a virtual absence of peroxisomes in liver and kidneys. This disease offers a unique opportunity to evaluate the relative importance of peroxisomes in bile acid biosynthesis. A child with Zellweger syndrome was studied in the present work. In accordance with previous work, there was a considerable accumulation of THCA, 3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxy-5 beta-cholestanoic acid (24-OH-THCA), 3 alpha, 7 alpha, 12 alpha-trihydroxy-27-carboxymethyl-5 beta-cholestan-26-oic acid (C29-dicarboxylic acid), and 3 alpha, 7 alpha-dihydroxy-5 beta-cholestanoic acid in serum. In addition, a tetrahydroxylated 5 beta-cholestanoic acid with all the hydroxyl groups in the steroid nucleus was found. 3H-Labeled 5 beta-cholestane-3 alpha, 7 alpha, 12 alpha-triol was administered intravenously together with 14C-labeled cholic acid. There was a rapid incorporation of 3H in THCA and a slow incorporation into cholic acid. The specific radioactivity of 3H in THCA was about one magnitude higher than that in cholic acid. The conversion was evaluated by following the increasing ratio between 3H and 14C in biliary cholic acid. The rate of incorporation of 3H in cholic acid was considerably less than previously reported in experiments with healthy subjects, and the maximal conversion of the triol into cholic acid was only 15-20%. About the same rate of conversion was found after oral administration of 3H-THCA. Both in the experiment with 3H-5 beta-cholestane-3 alpha, 7 alpha, 12 alpha-triol and with 3H-THCA, there was an efficient incorporation of 3H in the above unidentified tetrahydroxylated 5 beta-cholestanoic acid. There was only slow incorporation of radioactivity into 24-OH-THCA and into the C29-dicarboxylic acid. From the specific activity decay curve of 14C in cholic acid obtained after intravenous injection of 14C-cholic acid, the pool size of cholic acid was calculated to be 24 mg/m2 and the daily production rate to 9 mg/m2 per d. This corresponds to a reduction of approximately 85 and 90%, respectively, when compared with normal infants. It is concluded that liver peroxisomes are essential in the normal conversion of THCA to cholic acid. In the Zellweger syndrome this conversion is defective and as a consequence the accumulated THCA is either excreted as such or transformed into other metabolites by hydroxylation or side chain elongation. The accumulation of THCA, as well as the similar rate of conversion of 5 beta-cholestane-3 alpha,7 alpha.12 alpha-triol and THCA into cholic acid, support the contention that the 26-hydroxylase pathway with intermediate formation of THCA is the most important pathway for formation of cholic acid in man.

摘要

基于对大鼠肝脏的体外研究,我们最近提出,过氧化物酶体部分对于将3α,7α,12α-三羟基-5β-胆甾烷酸(THCA)氧化为胆酸最为重要。泽尔韦格脑肝肾综合征是一种致命的隐性常染色体疾病,其最典型的组织学特征是肝脏和肾脏中几乎没有过氧化物酶体。这种疾病为评估过氧化物酶体在胆汁酸生物合成中的相对重要性提供了一个独特的机会。在本研究中对一名患有泽尔韦格综合征的儿童进行了研究。与先前的研究一致,血清中THCA、3α,7α,12α,24-四羟基-5β-胆甾烷酸(24-OH-THCA)、3α,7α,12α-三羟基-27-羧甲基-5β-胆甾烷-26-酸(C29-二羧酸)和3α,7α-二羟基-5β-胆甾烷酸大量蓄积。此外,还发现了一种在甾体核中所有羟基都被羟基化的四羟基化5β-胆甾烷酸。将3H标记的5β-胆甾烷-3α,7α,12α-三醇与14C标记的胆酸一起静脉注射。3H迅速掺入THCA,而缓慢掺入胆酸。THCA中3H的比放射性比胆酸中的高约一个数量级。通过跟踪胆汁胆酸中3H与14C之间不断增加的比率来评估转化率。3H掺入胆酸的速率比先前在健康受试者实验中报道的要低得多,三醇转化为胆酸的最大转化率仅为15% - 20%。口服3H-THCA后发现了大致相同的转化率。在3H-5β-胆甾烷-3α,7α,12α-三醇和3H-THCA的实验中,3H都有效地掺入了上述未鉴定的四羟基化5β-胆甾烷酸中。放射性仅缓慢掺入24-OH-THCA和C29-二羧酸中。根据静脉注射14C-胆酸后获得的胆酸中14C的比活性衰减曲线,计算出胆酸的池大小为24mg/m2,每日生成率为9mg/m2 per d。与正常婴儿相比,这分别相当于减少了约85%和90%。结论是肝脏过氧化物酶体对于THCA正常转化为胆酸至关重要。在泽尔韦格综合征中,这种转化存在缺陷,因此积累的THCA要么原样排出,要么通过羟基化或侧链延长转化为其他代谢产物。THCA的积累以及5β-胆甾烷-3α,7α,12α-三醇和THCA转化为胆酸的相似速率,支持了这样的观点,即具有THCA中间形成的26-羟化酶途径是人类胆酸形成的最重要途径。