A multilevel analysis identifies the different relationships between amino acids and the competence of oocytes matured individually or in groups

Sci Rep. 2020 Sep 30;10(1):16082. doi: 10.1038/s41598-020-73225-7.

Abstract

High-protein diets contribute to an increase in urea follicular concentrations associated with decreased fertility. Urea has been shown to interfere with the epidermal growth factor (EGF)/EGFR system, which has been shown to have a beneficial effect during in vitro maturation (IVM) of oocytes. Of note, the number of cumulus-oocyte complexes (COCs) in the maturation medium can change the maturation and the developmental competence of COCs. Therefore, it was hypothesized that, the presence of urea and EGF may have a differential effect on the depletion/appearance of AAs and competence of COCs matured individually (I-IVM system) or in groups (G-IVM system). In the G-IVM system, COCs increased consumption (depletion) of AAs compared with other groups in the presence of high-level urea (40 mg/dl) + EGF (10 ng/ml). In the I-IVM system, the non-cleaved COCs depleted more AAs than the cleaved COCs, in particular in the presence of urea. The combination of urea and EGF increased the depletion of AAs in the G-IVM system. However, the EGF abrogated the urea-induced depletion of AAs by the I-IVM COCs. The use of N-acetyl-L-cysteine as an EGFR inhibitor canceled urea-induced depletion of AAs. This shows the inhibiting effect of urea over the EGF/EGFR system. In the presence of urea + EGF, COCs had a lower degree of developmental competence than control in both I- and G-IVM systems. Arginine had the best predictive power to identify highly competent COCs in the G-IVM system, while glutamine was the best predictor of the cleavage in the I-IVM system. In conclusion, this multi-level study shows that COCs matured individually or in groups may have different association with AAs metabolism. These findings provide new insights into the relationships between AA metabolism and the subsequent developmental competence of COCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism*
  • Amino Acids, Essential / metabolism
  • Animals
  • Cattle
  • Culture Media
  • Cumulus Cells / cytology
  • Cumulus Cells / metabolism
  • Epidermal Growth Factor / metabolism
  • Epidermal Growth Factor / pharmacology
  • Female
  • Gene Expression Regulation, Developmental
  • In Vitro Oocyte Maturation Techniques / methods
  • In Vitro Techniques
  • Molecular Docking Simulation
  • Multilevel Analysis
  • Oocytes / cytology
  • Oocytes / drug effects
  • Oocytes / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Urea / metabolism
  • Urea / pharmacology

Substances

  • Amino Acids
  • Amino Acids, Essential
  • Culture Media
  • RNA, Messenger
  • Epidermal Growth Factor
  • Urea