Sánchez-Guijo A, Blaschka C, Hartmann M F, Wrenzycki C, Wudy S A
Steroid Research & Mass Spectrometry Unit, Division of Pediatric Endocrinology & Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, 35392 Giessen, Germany.
Clinic for Veterinary Obstetrics, Gynecology and Andrology, Department of Molecular Reproductive Medicine, Justus Liebig University, Giessen, Germany.
J Steroid Biochem Mol Biol. 2016 Sep;162:117-25. doi: 10.1016/j.jsbmb.2016.02.020. Epub 2016 Feb 23.
Bile acids (BAs) are present in follicular fluid (FF) from humans and cattle. This fact has triggered an interest on the role BAs might play in folliculogenesis and their possible association with fertility. To achieve a better understanding about this subject, new methods are needed to provide reliable information about concentrations of the most important BAs in FF. In this context, liquid chromatography-tandem mass spectrometry (LC-MS/MS) offers high specificity with a relatively simple sample workup. We developed and validated a new assay for the quick profiling of the 9 most abundant BAs in follicular fluid from cattle. The method uses 200μl of FF and can quantify cholic acid (CA), chenodeoxycholic acid (CDCA), deoxycholic acid (DCA) and their glycine (G) and taurine (T) conjugates. Lithocholic acid (LCA), its conjugates GLCA and TLCA, and sulfated forms, were present in some samples, but their concentration was low compared to other BAs (in average, below 60ng/ml for LCA, GLCA or TLCA and below 20ng/ml for their corresponding sulfates). Method performance was studied at three quality controls for each compound in consonance with their physiological concentration. Excellent linearity and recovery were found for all compounds at every control level. Intra-day and between-day precisions (%CV) and accuracies (relative errors) were below 15% for all the compounds. Matrix effects were negligible for most of the analytes. Samples undergoing freeze-thaw showed no degradation of their BAs. The method makes use of a fused-core phenyl column coupled to a triple quadrupole tandem mass spectrometer to achieve chromatographic separation within 5min. We quantified BAs grouped in four different follicle sizes (3-5mm, 6-8mm, 9-14mm, >15mm), obtaining a similar relative BA profile for all the sizes, with CA always in higher concentration, ranging between 1600 and 18000ng/ml, approximately, followed by its conjugate glycocholic acid, GCA, which ranged between 800 and 9000ng/ml. The highest concentration in CA, DCA or CDCA was always detected in FF stemming from follicles of 6-8mm. To our knowledge, this is the first report in which BAs subspecies have been detected and quantified in bovine follicular fluid.
胆汁酸(BAs)存在于人和牛的卵泡液(FF)中。这一事实引发了人们对BAs在卵泡发生中可能发挥的作用及其与生育能力可能关联的兴趣。为了更好地理解这一主题,需要新的方法来提供关于卵泡液中最重要BAs浓度的可靠信息。在这种情况下,液相色谱 - 串联质谱法(LC-MS/MS)具有高特异性且样品预处理相对简单。我们开发并验证了一种新的检测方法,用于快速分析牛卵泡液中9种最丰富的BAs。该方法使用200μl卵泡液,可定量分析胆酸(CA)、鹅去氧胆酸(CDCA)、脱氧胆酸(DCA)及其甘氨酸(G)和牛磺酸(T)共轭物。石胆酸(LCA)及其共轭物GLCA和TLCA以及硫酸化形式在一些样品中存在,但其浓度与其他BAs相比很低(平均而言,LCA、GLCA或TLCA低于60ng/ml,其相应硫酸盐低于20ng/ml)。针对每种化合物的三种质量控制,根据其生理浓度研究了方法性能。在每个控制水平下,所有化合物均具有出色的线性和回收率。所有化合物的日内和日间精密度(%CV)和准确度(相对误差)均低于15%。大多数分析物的基质效应可忽略不计。经历冻融的样品其BAs未出现降解。该方法使用与三重四极杆串联质谱仪相连的熔融核苯基柱,可在5分钟内实现色谱分离。我们对四种不同卵泡大小(3 - 5mm、6 - 8mm、9 - 14mm、>15mm)的BAs进行了定量分析,所有大小的卵泡均获得了相似的相对BA谱,其中CA浓度始终较高,约在1600至18000ng/ml之间,其次是其共轭物甘氨胆酸(GCA),浓度在800至9000ng/ml之间。在6 - 8mm卵泡的卵泡液中始终检测到CA、DCA或CDCA的最高浓度。据我们所知,这是首次在牛卵泡液中检测和定量分析BAs亚种的报告。