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Mol Genet Metab. 2013 Sep-Oct;110(1-2):176-8. doi: 10.1016/j.ymgme.2013.04.004. Epub 2013 Apr 10.
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Pharmacol Biochem Behav. 2013 May;106:101-8. doi: 10.1016/j.pbb.2013.03.007. Epub 2013 Mar 26.
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Biochem Pharmacol. 2013 Jul 1;86(1):43-55. doi: 10.1016/j.bcp.2013.03.003. Epub 2013 Mar 13.
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Hepatic isoprenoid metabolism in a rat model of Smith-Lemli-Opitz Syndrome.史密斯-勒米-奥皮茨综合征大鼠模型中的肝脏类异戊二烯代谢
Lipids. 2013 Mar;48(3):219-29. doi: 10.1007/s11745-013-3762-x. Epub 2013 Jan 30.
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Atypical antipsychotics alter cholesterol and fatty acid metabolism in vitro.非典型抗精神病药物会改变胆固醇和脂肪酸的代谢。
J Lipid Res. 2013 Feb;54(2):310-24. doi: 10.1194/jlr.M026948. Epub 2012 Nov 21.
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Assays of plasma dehydrocholesteryl esters and oxysterols from Smith-Lemli-Opitz syndrome patients.Smith-Lemli-Opitz 综合征患者血浆脱氢胆固醇酯和氧化固醇的检测。
J Lipid Res. 2013 Jan;54(1):244-53. doi: 10.1194/jlr.M031732. Epub 2012 Oct 16.
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A comprehensive method for extraction and quantitative analysis of sterols and secosteroids from human plasma.一种从人血浆中提取和定量分析甾体和甾族化合物的综合方法。
J Lipid Res. 2012 Jul;53(7):1399-409. doi: 10.1194/jlr.D022285. Epub 2012 Apr 19.
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DHCEO accumulation is a critical mediator of pathophysiology in a Smith-Lemli-Opitz syndrome model.DHCEO 堆积是 Smith-Lemli-Opitz 综合征模型中病理生理学的关键介质。
Neurobiol Dis. 2012 Mar;45(3):923-9. doi: 10.1016/j.nbd.2011.12.011. Epub 2011 Dec 11.
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Biosynthesis of cholesterol and other sterols.胆固醇及其他甾醇的生物合成。
Chem Rev. 2011 Oct 12;111(10):6423-51. doi: 10.1021/cr200021m. Epub 2011 Sep 8.

用于 Smith-Lemli-Opitz 综合征研究的 7-脱氢胆固醇分析的高灵敏度方法。

A highly sensitive method for analysis of 7-dehydrocholesterol for the study of Smith-Lemli-Opitz syndrome.

机构信息

Department of Chemistry, Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, TN 37235.

出版信息

J Lipid Res. 2014 Feb;55(2):329-37. doi: 10.1194/jlr.D043877. Epub 2013 Nov 20.

DOI:10.1194/jlr.D043877
PMID:24259532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3886672/
Abstract

We describe a highly sensitive method for the detection of 7-dehydrocholesterol (7-DHC), the biosynthetic precursor of cholesterol, based on its reactivity with 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) in a Diels-Alder cycloaddition reaction. Samples of biological tissues and fluids with added deuterium-labeled internal standards were derivatized with PTAD and analyzed by LC-MS. This protocol permits fast processing of samples, short chromatography times, and high sensitivity. We applied this method to the analysis of cells, blood, and tissues from several sources, including human plasma. Another innovative aspect of this study is that it provides a reliable and highly reproducible measurement of 7-DHC in 7-dehydrocholesterol reductase (Dhcr7)-HET mouse (a model for Smith-Lemli-Opitz syndrome) samples, showing regional differences in the brain tissue. We found that the levels of 7-DHC are consistently higher in Dhcr7-HET mice than in controls, with the spinal cord and peripheral nerve showing the biggest differences. In addition to 7-DHC, sensitive analysis of desmosterol in tissues and blood was also accomplished with this PTAD method by assaying adducts formed from the PTAD "ene" reaction. The method reported here may provide a highly sensitive and high throughput way to identify at-risk populations having errors in cholesterol biosynthesis.

摘要

我们描述了一种基于 7-脱氢胆固醇(7-DHC)与 4-苯基-1,2,4-三唑啉-3,5-二酮(PTAD)在 Diels-Alder 环加成反应中的反应性,来检测胆固醇生物合成前体 7-DHC 的高灵敏度方法。添加氘标记内部标准品的生物组织和流体样本经过 PTAD 衍生化后,通过 LC-MS 进行分析。该方案允许快速处理样品,缩短色谱时间,提高灵敏度。我们将这种方法应用于来自多个来源的细胞、血液和组织的分析,包括人血浆。本研究的另一个创新点是,它提供了一种可靠且高度重现性的 7-脱氢胆固醇还原酶(Dhcr7)-杂合子(用于 Smith-Lemli-Opitz 综合征的模型)样本中 7-DHC 的测量方法,显示出脑组织中的区域差异。我们发现,7-DHC 水平在 Dhcr7-杂合子小鼠中始终高于对照组,脊髓和周围神经的差异最大。除了 7-DHC 之外,通过测定 PTAD“ene”反应形成的加合物,还可以用这种 PTAD 方法对组织和血液中的 desmosterol 进行敏感分析。这里报道的方法可能为鉴定胆固醇生物合成错误的高危人群提供一种高度敏感和高通量的方法。