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Mol Cell Endocrinol ; 420: 46-56, 2016 Jan 15.
Article in English | MEDLINE | ID: mdl-26628038

ABSTRACT

Supplementation of in-vitro maturation medium with reagents that inhibit meiotic resumption whilst supporting normal function of cumulus cell-oocyte complexes (COC) is challenging. This study compared the in-vitro effects of synthetic and physiologically-relevant reagents on meiotic resumption, gap junction activity and gene expression of rat COC. Higher doses of forskolin reduced gap junction activity. Whilst addition of phosphodiesterase inhibitors initially promoted gap junction activity, this decreased with time in-vitro. Moreover despite oocytes remaining in meiotic arrest, there was a concomitant decline in expression of genes critical for oocyte maturation, and evidence of a reduction in overall transcription rate. Similarly, supplementing media with C-type natriuretic peptide and/or oestradiol delayed meiotic resumption and only initially maintained gap junction activity. In contrast, several key genes were stimulated and overall transcription rates remained constant with time in-vitro. In summary, supplementation of media with physiologically-relevant reagents may better enable normal functions of the COC.


Subject(s)
Coloring Agents/metabolism , Cumulus Cells/cytology , Cyclic AMP/pharmacology , Cyclic GMP/pharmacology , Extracellular Space/metabolism , Gene Expression Regulation/drug effects , Oocytes/cytology , Animals , Carbenoxolone/pharmacology , Colforsin/pharmacology , Connexin 43/metabolism , Cumulus Cells/drug effects , Cumulus Cells/metabolism , Cyclic Nucleotide Phosphodiesterases, Type 3/metabolism , Female , Gap Junctions/drug effects , Gap Junctions/metabolism , Genetic Association Studies , Meiosis/drug effects , Oocytes/drug effects , Oocytes/metabolism , Phosphodiesterase Inhibitors/pharmacology , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats, Sprague-Dawley , Time Factors
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