N-octanoylated ghrelin peptide inhibits bovine oocyte meiotic resumption

•50 ng/mL ghrelin could inhibit bovine oocytes germinal vesicle breakdown.•Increased cAMP and cGMP levels in CCs and DOs contributed to this inhibition.•Inhibitory ghrelin benefits the developmental competence of matured oocytes.•Ghrelin could act as a pharmaceutical meiosis inhibitor for bovine ooc...

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Veröffentlicht in:General and comparative endocrinology 2018-07, Vol.263, p.7-11
Hauptverfasser: Xu, X.L., Bai, J.H., Feng, T., Xiao, L.L., Song, Y.Q., Xiao, Y.X., Liu, Y.
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Sprache:eng
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Zusammenfassung:•50 ng/mL ghrelin could inhibit bovine oocytes germinal vesicle breakdown.•Increased cAMP and cGMP levels in CCs and DOs contributed to this inhibition.•Inhibitory ghrelin benefits the developmental competence of matured oocytes.•Ghrelin could act as a pharmaceutical meiosis inhibitor for bovine oocytes. Studies have shown that ghrelin plays an important role in the mammalian reproductive system, including the central, gonadal levels, and also during in vitro maturation of oocytes; however, the functions of ghrelin in bovine oocyte meiosis require further investigation. We aimed to evaluate the effects of an n-octanoylated ghrelin peptide on oocyte meiotic resumption and the developmental competence of mature oocytes in vitro. design: The expression of GHRL (encoding ghrelin) mRNA and its receptor (the growth hormone secretagogue receptor, GHSR) in the cumulus-oocyte complex (COCs), denuded oocytes (DOs), and cumulus cells (CCs) was assessed using quantitative real-time reverse transcription PCR (qRT-PCR), and the effects of the n-octanoylated ghrelin peptide on meiotic resumption were studied at four different doses (0, 10, 50, and 100 ng/mL) in a 6 h culture system. qRT-PCR analysis showed that GHRL and GHSR mRNAs were expressed in all tested samples; however, GHRL was predominantly expressed in DOs, and GHSR was predominantly expressed in CCs. Germinal vesicle breakdown was inhibited significantly by 50 ng/mL ghrelin compared with that in the negative control (P 
ISSN:0016-6480
1095-6840
DOI:10.1016/j.ygcen.2018.04.016