Profiling of bile acids in bovine follicular fluid by fused-core-LC-MS/MS

J Steroid Biochem Mol Biol. 2016 Sep:162:117-25. doi: 10.1016/j.jsbmb.2016.02.020. Epub 2016 Feb 23.

Abstract

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.

Keywords: Bile acids; Bovine fertility; Follicular fluid; Fused-core technology; Liquid chromatography–mass spectrometry.

Publication types

  • Validation Study

MeSH terms

  • Animals
  • Bile Acids and Salts / analysis*
  • Cattle
  • Chenodeoxycholic Acid / analysis
  • Cholic Acid / analysis
  • Chromatography, High Pressure Liquid / methods
  • Deoxycholic Acid / analysis
  • Female
  • Follicular Fluid / chemistry*
  • Limit of Detection
  • Lithocholic Acid / analysis
  • Spectrometry, Mass, Electrospray Ionization / methods
  • Tandem Mass Spectrometry / methods

Substances

  • Bile Acids and Salts
  • Deoxycholic Acid
  • Chenodeoxycholic Acid
  • Lithocholic Acid
  • Cholic Acid