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筛查史密斯-利姆利-奥皮茨综合征中异常的胆固醇生物合成:通过紫外光谱法快速测定血浆7-脱氢胆固醇

Screening for abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz syndrome: rapid determination of plasma 7-dehydrocholesterol by ultraviolet spectrometry.

作者信息

Honda A, Batta A K, Salen G, Tint G S, Chen T S, Shefer S

机构信息

Department of Medicine, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, USA.

出版信息

Am J Med Genet. 1997 Jan 31;68(3):288-93. doi: 10.1002/(sici)1096-8628(19970131)68:3<288::aid-ajmg8>3.0.co;2-i.

Abstract

The Smith-Lemli-Opitz syndrome (SLOS) is a common condition caused by deficiency of 7-dehydrocholesterol delta 7-reductase. The syndrome can usually be diagnosed by demonstrating markedly increased plasma concentrations of the cholesterol precursor, 7-dehydrocholesterol. We describe a simple and rapid method for detection of plasma 7-dehydrocholesterol by use of ultraviolet (UV) spectrometry. Lipids were extracted from plasma by addition of ethanol and n-hexane, and the n-hexane phase was directly subjected to spectrometry. The absorption maxima characteristics of 7-dehydrocholesterol (lambda max 271, 282, and 294 nm) were observed in patients' plasma but not in controls. For quantitative measurements, absorbance at 282 nm was used. Since this absorbance is the sum of the absorbance derived from 7-dehydrocholesterol and background absorbance, the concentrations of 7-dehydrocholesterol in various plasma samples were quantified by subtracting estimated background absorbance at 282 nm from observed absorbance at 282 nm. The results correlated well with total (free plus esterified) 7-dehydrocholesterol concentrations measured by gas-liquid chromatographic method. The UV spectrometric assay was sensitive enough to detect increased 7-dehydrocholesterol in cultured skin fibroblasts from patients grown in delipidated medium. The present method will make it possible to screen plasma or fibroblasts to detect the syndrome rapidly in general clinical laboratories.

摘要

史密斯-利姆利-奥皮茨综合征(SLOS)是一种由7-脱氢胆固醇δ7-还原酶缺乏引起的常见病症。该综合征通常可通过证明胆固醇前体7-脱氢胆固醇的血浆浓度显著升高来诊断。我们描述了一种使用紫外(UV)光谱法检测血浆7-脱氢胆固醇的简单快速方法。通过加入乙醇和正己烷从血浆中提取脂质,正己烷相直接进行光谱分析。在患者血浆中观察到了7-脱氢胆固醇的吸收峰特征(最大吸收波长271、282和294nm),而在对照中未观察到。对于定量测量,使用282nm处的吸光度。由于该吸光度是来自7-脱氢胆固醇的吸光度与背景吸光度之和,通过从282nm处观察到的吸光度中减去估计的282nm处背景吸光度,对各种血浆样品中7-脱氢胆固醇的浓度进行定量。结果与通过气液色谱法测量的总(游离加酯化)7-脱氢胆固醇浓度相关性良好。紫外光谱测定法足够灵敏,能够检测在无脂培养基中培养的患者皮肤成纤维细胞中升高的7-脱氢胆固醇。本方法将使在一般临床实验室中快速筛查血浆或成纤维细胞以检测该综合征成为可能。

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