Nilsson Maria E, Vandenput Liesbeth, Tivesten Åsa, Norlén Anna-Karin, Lagerquist Marie K, Windahl Sara H, Börjesson Anna E, Farman Helen H, Poutanen Matti, Benrick Anna, Maliqueo Manuel, Stener-Victorin Elisabet, Ryberg Henrik, Ohlsson Claes
Centre for Bone and Arthritis Research (M.E.N., L.V., M.K.L., S.H.W., A.E.B., H.H.F., M.P., C.O.), Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Wallenberg Laboratory for Cardiovascular and Metabolic Research (Å.T.), Institute of Medicine, Department of Physiology (A.B., M.M., E.S.-V.), Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg SE-413 45, Sweden; Department of Clinical Chemistry (M.E.N., A.-K.N., H.R.), Sahlgrenska University Hospital, Gothenburg SE-413 45, Sweden; and Department of Physiology (M.P.), Institute of Biomedicine and Turku Center for Disease Modeling, University of Turku, Turku FI-20014, Finland.
Endocrinology. 2015 Jul;156(7):2492-502. doi: 10.1210/en.2014-1890. Epub 2015 Apr 9.
Accurate measurement of sex steroid concentrations in rodent serum is essential to evaluate mouse and rat models for sex steroid-related disorders. The aim of the present study was to develop a sensitive and specific gas chromatography-tandem mass spectrometry (GC-MS/MS) method to assess a comprehensive sex steroid profile in rodent serum. A major effort was invested in reaching an exceptionally high sensitivity for measuring serum estradiol concentrations. We established a GC-MS/MS assay with a lower limit of detection for estradiol, estrone, T, DHT, progesterone, androstenedione, and dehydroepiandrosterone of 0.3, 0.5, 4.0, 1.6, 8, 4.0, and 50 pg/mL, respectively, whereas the corresponding values for the lower limit of quantification were 0.5, 0.5, 8, 2.5, 74, 12, and 400 pg/mL, respectively. Calibration curves were linear, intra- and interassay coefficients of variation were low, and accuracy was excellent for all analytes. The established assay was used to accurately measure a comprehensive sex steroid profile in female rats and mice according to estrous cycle phase. In addition, we characterized the impact of age, sex, gonadectomy, and estradiol treatment on serum concentrations of these sex hormones in mice. In conclusion, we have established a highly sensitive and specific GC-MS/MS method to assess a comprehensive sex steroid profile in rodent serum in a single run. This GC-MS/MS assay has, to the best of our knowledge, the best detectability reported for estradiol. Our method therefore represents an ideal tool to characterize sex steroid metabolism in a variety of sex steroid-related rodent models and in human samples with low estradiol levels.
准确测量啮齿动物血清中的性类固醇浓度对于评估与性类固醇相关疾病的小鼠和大鼠模型至关重要。本研究的目的是开发一种灵敏且特异的气相色谱 - 串联质谱法(GC-MS/MS),以评估啮齿动物血清中的综合性类固醇谱。在提高测量血清雌二醇浓度的灵敏度方面投入了大量精力。我们建立了一种GC-MS/MS测定法,其对雌二醇、雌酮、睾酮(T)、双氢睾酮(DHT)、孕酮、雄烯二酮和脱氢表雄酮的检测下限分别为0.3、0.5、4.0、1.6、8、4.0和50 pg/mL,而相应的定量下限值分别为0.5、0.5、8、2.5、74、12和400 pg/mL。校准曲线呈线性,批内和批间变异系数较低,所有分析物的准确度都很高。所建立的测定法用于根据动情周期阶段准确测量雌性大鼠和小鼠的综合性类固醇谱。此外,我们还研究了年龄、性别、去势和雌二醇处理对小鼠这些性激素血清浓度的影响。总之,我们建立了一种高度灵敏且特异的GC-MS/MS方法,可单次运行评估啮齿动物血清中的综合性类固醇谱。据我们所知,这种GC-MS/MS测定法对雌二醇的检测能力是已报道的最佳水平。因此,我们的方法是表征各种与性类固醇相关的啮齿动物模型以及低雌二醇水平人类样本中性类固醇代谢的理想工具。