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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Utility of isolated hepatocytes and radio-HPLC-MSn for the analysis of the metabolic fate of 19-nortestosterone laurate in cattle
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Utility of isolated hepatocytes and radio-HPLC-MSn for the analysis of the metabolic fate of 19-nortestosterone laurate in cattle

机译:分离的肝细胞和放射HPLC-MSn在牛19-去甲睾酮月桂酸酯代谢结果分析中的应用

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摘要

The metabolic fate of 19-nortestosterone laurate in cattle was investigated to evaluate target analyte(s) appropriate to surveillance for illicit use as a growth promoting agent. Bovine hepatocytes were incubated with either [H-3] 19-nortestosterone laurate (19-NTL; 4-estren-17 beta-laurate-3-one) or [H-3] 19-nortestosterone (19-NT; 4-estren-17 beta-ol-3-one; nandrolone). Hepatocyte medium was extracted with solid phase Clx media and analysed by narrow bore radio-HPLC-MSn (LCQ, Finnigan) to evaluate the structure of metabolites of 19-NTL and 19-NT. Radio-HPLC of hepatocyte medium extracts following incubation with [3H]19-NTL confirmed that the first step of biotransformation in liver was hydrolysis of the fatty acid ester to release [3H]19-NT, which, in turn, was converted into a range of metabolites of diverse polarity. Hydrolysis of hepatocyte medium extracts with P-glucuronidase (Helix pomatia) indicated that some of these metabolites were glucuronide or sulfate conjugates. Structural analysis of unconjugated metabolities by positive-ion atmospheric pressure chemical ionisation MS2 and comparison with available reference preparations indicated biotransformation of 19-NT to 4-estren-17 alpha-ol-3-one, 4-estren-3,17-dione (major metabolite after 1 h), n-hydroxy-4-estren-3, 17-dione, n-hydroxy-4-estren-17-ol-3-one, beta-estran-3 alpha-ol-17-one (noretiocholanolone) and 5 beta-estran-3 alpha,17 beta-ol(major metabolite after 4 h). Conjugated metabolites were analysed by electrospray ionization, which revealed the presence of glucuronide conjugates of alpha-(trace) and P-epimers of 19-NT, n-hydroxy-4-estren-3, 17-dione, n-hydroxy-4-estren-17-ol-3-one and 5 beta-estran-3 alpha,17 beta-diol. These studies provide a clear indication of the route of hepatic metabolism in the bovine, which may now be readily substantiated by reference to samples, such as urine or bile, derived from animals treated with unlabelled 19-NTL. [References: 19]
机译:研究了牛体内19-去甲睾丸激素月桂酸酯的代谢命运,以评估适于监测是否非法用作生长促进剂的目标分析物。牛肝细胞与[H-3] 19-月桂睾酮月桂酸酯(19-NTL; 4-雌烯-17β-月桂酸酯-3-one)或[H-3] 19-月睾酮(19-NT; 4-雌激素)孵育-17 beta-ol-3-one; Nandrolone)。用固相Clx培养基提取肝细胞培养基,并通过窄孔放射性HPLC-MSn(LCQ,Finnigan)分析以评估19-NTL和19-NT的代谢物结构。与[3H] 19-NTL孵育后,对肝细胞培养基提取物进行放射HPLC证实,肝脏中生物转化的第一步是脂肪酸酯水解以释放[3H] 19-NT,然后将其转化为各种极性的代谢产物。用P-葡萄糖醛酸苷酶(Helix pomatia)水解肝细胞培养基提取物表明,其中一些代谢产物是葡萄糖醛酸苷或硫酸盐结合物。通过阳离子大气压化学电离MS2对未结合代谢物进行结构分析,并与可用的参考制剂进行比较,结果表明19-NT可生物转化为4-estren-17α-ol-3-one,4-estren-3,17-dione( 1小时后的主要代谢产物),n-羟基-4-雌烯3、17-二酮,n-羟基-4-雌烯17-ol-3-一个,β-雌三烯3 alpha-ol-17-一个( Noretiocholanolanol)和5 beta-estran-3 alpha,17 beta-ol(4 h后主要代谢产物)。通过电喷雾电离分析共轭的代谢物,结果显示存在19-NT,n-羟基-4-雌烯-3、17-二酮,n-羟基-4-的α-(痕量)和P-表位的葡糖醛酸苷共轭物。 estren-17-ol-3-one和5 beta-estran-3 alpha,17 beta-diol。这些研究清楚地表明了牛体内肝脏的代谢途径,现在可以很容易地通过参考样品(如尿液或胆汁)来证实,这些样品来自未标记19-NTL的动物。 [参考:19]

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