Javascript must be enabled to continue!
Inactivation of glucocorticoids by 11β-hydroxysteroid dehydrogenase enzymes increases during the meiotic maturation of porcine oocytes
View through CrossRef
Abstract
Recent reports have shown that glucocorticoids can modulate oocyte maturation in both teleost fish and mammals. Within potential target cells, the actions of physiological glucocorticoids are modulated by 11β-hydroxysteroid dehydrogenase (HSD11B) isoenzymes that catalyse the interconversion of cortisol and cortisone. Hence, the objective of this study was to establish whether HSD11B enzymes mediate cortisol–cortisone metabolism in porcine oocytes and, if so, whether the rate of glucocorticoid metabolism changes during oocyte maturation. Enzyme activities were measured in cumulus–oocyte complexes (COCs) and denuded oocytes (DOs) using radiometric conversion assays. While COCs and DOs oxidised cortisol to inert cortisone, there was no detectable regeneration of cortisol from cortisone. The rate of cortisol oxidation was higher in expanded COCs than in compact COCs containing germinal vesicle (GV) stage oocytes (111±6 vs 2041±115 fmol cortisone/oocyte.24 h; P<0.001). Likewise, HSD11B activities were 17±1 fold higher in DOs from expanded COCs than in those from compact COCs (P<0.001). When GV stage oocytes were subject to a 48 h in vitro maturation protocol, the enzyme activities were significantly increased from 146±18 to 1857±276 fmol cortisone/oocyte.24 h in GV versus MII stage oocytes respectively (P<0.001). Cortisol metabolism was inhibited by established pharmacological inhibitors of HSD11B (glycyrrhetinic acid and carbenoxolone), and by porcine follicular and ovarian cyst fluid. We conclude that an HSD11B enzyme (or enzymes) functions within porcine oocytes to oxidise cortisol, and that this enzymatic inactivation of cortisol increases during oocyte maturation.
Oxford University Press (OUP)
Title: Inactivation of glucocorticoids by 11β-hydroxysteroid dehydrogenase enzymes increases during the meiotic maturation of porcine oocytes
Description:
Abstract
Recent reports have shown that glucocorticoids can modulate oocyte maturation in both teleost fish and mammals.
Within potential target cells, the actions of physiological glucocorticoids are modulated by 11β-hydroxysteroid dehydrogenase (HSD11B) isoenzymes that catalyse the interconversion of cortisol and cortisone.
Hence, the objective of this study was to establish whether HSD11B enzymes mediate cortisol–cortisone metabolism in porcine oocytes and, if so, whether the rate of glucocorticoid metabolism changes during oocyte maturation.
Enzyme activities were measured in cumulus–oocyte complexes (COCs) and denuded oocytes (DOs) using radiometric conversion assays.
While COCs and DOs oxidised cortisol to inert cortisone, there was no detectable regeneration of cortisol from cortisone.
The rate of cortisol oxidation was higher in expanded COCs than in compact COCs containing germinal vesicle (GV) stage oocytes (111±6 vs 2041±115 fmol cortisone/oocyte.
24 h; P<0.
001).
Likewise, HSD11B activities were 17±1 fold higher in DOs from expanded COCs than in those from compact COCs (P<0.
001).
When GV stage oocytes were subject to a 48 h in vitro maturation protocol, the enzyme activities were significantly increased from 146±18 to 1857±276 fmol cortisone/oocyte.
24 h in GV versus MII stage oocytes respectively (P<0.
001).
Cortisol metabolism was inhibited by established pharmacological inhibitors of HSD11B (glycyrrhetinic acid and carbenoxolone), and by porcine follicular and ovarian cyst fluid.
We conclude that an HSD11B enzyme (or enzymes) functions within porcine oocytes to oxidise cortisol, and that this enzymatic inactivation of cortisol increases during oocyte maturation.
Related Results
UVB induces epidermal 11β‐hydroxysteroid dehydrogenase type 1 activity in vivo
UVB induces epidermal 11β‐hydroxysteroid dehydrogenase type 1 activity in vivo
AbstractDetrimental consequences of ultraviolet radiation (UVR) in skin include photoageing, immunosuppression and photocarcinogenesis, processes also significantly regulated by lo...
O-105 Chromatin accessibility of oocytes contributes to PCOS transgenerational inheritance
O-105 Chromatin accessibility of oocytes contributes to PCOS transgenerational inheritance
Abstract
Study question
What is the underlying mechanism contributing to the transgenerational defects of oocytes and embryos of...
Resection of DNA double strand breaks in the germline of Caenorhabditis elegans
Resection of DNA double strand breaks in the germline of Caenorhabditis elegans
<p>Repair of double-strand DNA breaks (DSBs) by the homologous recombination (HR) pathway results in crossovers (COs) required for a successful first meiotic division. DSB re...
3α‐Hydroxysteroid: NAD Oxidoreductase Activity in Crystalline Preparations of 20β‐Hydroxysteroid: NAD Oxidoreductase
3α‐Hydroxysteroid: NAD Oxidoreductase Activity in Crystalline Preparations of 20β‐Hydroxysteroid: NAD Oxidoreductase
Crystalline 20β‐hydroxysteroid: NAD oxidoreductase preparations from Streptomyces hydrogenans were shown to have 3α‐hydroxysteroid: NAD oxidoreductase activity. Compounds of both t...
Analyses of EMI functions on meiotic maturation of porcine oocytes
Analyses of EMI functions on meiotic maturation of porcine oocytes
SUMMARYCyclin B (CCNB) accumulation is essential for regulating maturation/M‐phase promoting factor activity during vertebrate oocyte maturation. Anaphase‐promoting‐complex/cycloso...
Cryopreservation of Immature Porcine Oocytes Using Open Pulled Straw Vitrification
Cryopreservation of Immature Porcine Oocytes Using Open Pulled Straw Vitrification
The aims of this study were to investigate the meiotic competence of immature porcine oocytes following open pulled straw (OPS) vitrification and warming and also to test the effic...
Sperm binding capacity and ultrastructure of the zona pellucida of stored canine oocytes
Sperm binding capacity and ultrastructure of the zona pellucida of stored canine oocytes
Abstract
Sperm binding to the zona pellucida is a prerequisite for fertilization, and tests that evaluate this function have been described for several species. W...
Mitochondrial disorders in neuromuscular pathology
Mitochondrial disorders in neuromuscular pathology
Introduction. With the advent of new drugs — analogues of mitochondrial metabolites, the widespread introduction into practice of research methods for assessing the function of mit...

