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Abstract
Testosterone is a hormone that plays a key role in carbohydrate, fat, and protein metabolism. Testosterone deficiency is associated with multiple comorbidities, e.g., metabolic syndrome and type 2 diabetes. Despite its importance in many metabolic pathways, the mechanisms by which it controls metabolism are not fully understood. The present study investigated the short-term metabolic changes of pharmacologically induced castration and, subsequently, testosterone supplementation in healthy young males. Thirty subjects were submitted to testosterone depletion (TD) followed by testosterone supplementation (TS). Plasma samples were collected three times corresponding to basal, low, and restored testosterone levels. An untargeted metabolomics study was performed by liquid chromatography–high resolution mass spectrometry (UHPLC–HRMS) to monitor the metabolic changes induced by the altered hormone levels. Our results demonstrated that TD was associated with major metabolic changes partially restored by TS. Carnitine and amino acid metabolism were the metabolic pathways most impacted by variations in testosterone. Furthermore, our results also indicated that LH and FSH might strongly alter the plasma levels of indoles and lipids, especially glycerophospholipids and sphingolipids. Our results demonstrated major metabolic changes induced by low testosterone that may be important for understanding the mechanisms behind the association of testosterone deficiency and its comorbidities.
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1 Federal University of Rio de Janeiro, Laboratory of Proteomics, LADETEC, Institute of Chemistry, Rio de Janeiro, Brazil (GRID:grid.8536.8) (ISNI:0000 0001 2294 473X); Federal University of Rio de Janeiro, Proteomics Unit, Institute of Chemistry, Rio de Janeiro, Brazil (GRID:grid.8536.8) (ISNI:0000 0001 2294 473X)
2 Lund University, Clinical Protein Science and Imaging, Department of Biomedical Engineering, Biomedical Centre, Lund, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); Lund University, Skåne University Hospital Malmö, Section for Clinical Chemistry, Department of Translational Medicine, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361)
3 Federal University of Rio de Janeiro, Laboratory of Proteomics, LADETEC, Institute of Chemistry, Rio de Janeiro, Brazil (GRID:grid.8536.8) (ISNI:0000 0001 2294 473X); National Institute of Cardiology, Rio de Janeiro, Brazil (GRID:grid.419171.b) (ISNI:0000 0004 0481 7106)
4 Lund University, Clinical Protein Science and Imaging, Department of Biomedical Engineering, Biomedical Centre, Lund, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361)
5 Lund University, Clinical Protein Science and Imaging, Department of Biomedical Engineering, Biomedical Centre, Lund, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); Tokyo Medical University, First Department of Surgery, Shinjuku-ku, Japan (GRID:grid.410793.8) (ISNI:0000 0001 0663 3325)
6 Lund University, Molecular Reproductive Medicine, Department of Translational Medicine, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361)
7 Federal University of Rio de Janeiro, Proteomics Unit, Institute of Chemistry, Rio de Janeiro, Brazil (GRID:grid.8536.8) (ISNI:0000 0001 2294 473X)