Pre-estrus progesterone does not affect post-estrus luminal metabolome in cross-bred beef cows

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Authors:
Felipe A. C. C. SilvaF Silva, Department of Animal Sciences, University of Florida, Gainesville, United States

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Thiago MartinsT Martins, Department of Animal Sciences, University of Florida, Gainesville, United States

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Mariana SponchiadoM Sponchiado, Animal Sciences, University of Florida, Gainesville, United States

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Cecilia C. RochaC Rocha, Department of Animal Sciences, University of Florida, Gainesville, United States

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Nadia AshrafiN Ashrafi, Metabolomics Department, Beaumont Research Institute, Royal Oak, United States

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Stewart F. GrahamS Graham, Metabolomics Department, Beaumont Research Institute, Royal Oak, United States

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Ky PohlerK Pohler, Animal Science, Texas A and M University System, College Station, United States

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Francisco PeñagaricanoF Peñagaricano, Department of Animal and Dairy Sciences, University of Wisconsin-Madison, Madison, United States

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Angela Gonella-DiazaA Gonella-Diaza, Animal Sciences, University of Florida North Florida Research and Education Center, Marianna, United States

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Mario BinelliM Binelli, Department of Animal Sciences, University of Florida, Gainesville, United States

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Correspondence: Mario Binelli, Email: mario.binelli@ufl.edu
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In cattle, the concentration of sex steroids modulates uterine function, which is reflected in the composition of the luminal metabolome. Ultimately, the uterine luminal metabolome influences embryonic growth and development. Our objectives were (1) to compare the luminal metabolome 4, 7, and 14 days after estrus of cows that were exposed to greater (HP4; n = 16) vs. lower (LP4; n = 24) concentrations of progesterone before displaying estrus and ovulating spontaneously and (2) to identify changes in the luminal concentration of metabolites across these time points. Luminal epithelial cells and fluid were collected using a cytology brush and gene expression and metabolite concentrations were assessed by RNAseq and targeted mass spectrometry, respectively. Metabolome profile was similar between treatments within each of days 4, 7, and 14 (FDR ≥ 0.1). Concentrations of 53 metabolites changed, independent of treatment, across the diestrus. Metabolites were mostly lipids (40 out 53) and the greatest concentrations were at d 14 (FDR ≤ 0.1). On d 7, the concentration of putrescine and the gene expression of ODC1, PAOX, SLC3A2, and SAT1 increased (P ≤ 0.05). On d 14, the concentration of three ceramides, four glucosylceramides, and 12 sphingomyelins and the expression of SGMS2 were increased, in addition to the concentration of choline and 20 phosphatidylcholines. Collectively, the post-estrus concentration of luminal metabolites changed dynamically, independent of the concentration of sex steroids on the previous cycle, and the greatest magnitude changes were on day 14, when lipid metabolism was the most enriched pathway.