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1.
Reprod Domest Anim ; 49(6): 1068-73, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25307885

RESUMO

Oocyte maturation depends on the metabolic activity of cumulus-oocyte complex (COC) that performs nutritive and regulatory functions during this process. In this work, the enzymes [phosphofructokinase (PFK) and malate dehydrogenase (MDH)] were tested to elucidate the metabolic profile of porcine COCs during the in vitro maturation (IVM). Enzymatic activity was expressed in U/COC and U/mg protein (specific activity) as mean ± SEM. In vitro maturation was performed with 2-oxoglutarate (5, 10 and 20 mm) or hydroxymalonate (30, 60 and 100 mm) inhibitors of PFK and MDH, respectively. The PFK and MDH activities (U) remained constant during maturation. For PFK, the U were (2.48 ± 0.23) 10(-5) and (2.54 ± 0.32) 10(-5) , and for MDH, the U were (4.72 ± 0.42) 10(-5) and (4.38 ± 0.25) 10(-5) for immature and in vitro matured COCs, respectively. The specific activities were significantly lower after IVM, for PFK (4.29 ± 0.48) 10(-3) and (0.94 ± 0.12) 10(-3) , and for MDH (9.08 ± 0.93) 10(-3) and (1.89 ± 0.10) 10(-3) for immature and in vitro matured COCs, respectively. In vitro maturation percentages and enzymatic activity diminished with 20 mm 2-oxoglutarate or 60 mm hydroxymalonate (p < 0.05). Viability was not affected by any concentration of the inhibitors evaluated. The U remained unchanged during IVM; however, the increase in the total protein content per COC provoked a decrease in the specific activity of both enzymes. Phosphofructokinase and MDH necessary for oocyte IVM would be already present in the immature oocyte. The presence of inhibitors of these enzymes impairs the meiotic maturation. Therefore, the participation of these enzymes in the energy metabolism of the porcine oocyte during IVM is confirmed in this study.


Assuntos
Técnicas de Maturação in Vitro de Oócitos/veterinária , Malato Desidrogenase/metabolismo , Oócitos/enzimologia , Fosfofrutoquinases/metabolismo , Suínos/fisiologia , Animais , Sobrevivência Celular , Células do Cúmulo , Regulação Enzimológica da Expressão Gênica/fisiologia , Ácidos Cetoglutáricos/farmacologia , Malato Desidrogenase/antagonistas & inibidores , Malato Desidrogenase/genética , Meiose/fisiologia , Fosfofrutoquinases/antagonistas & inibidores , Fosfofrutoquinases/genética , Tartronatos/farmacologia
2.
Cryobiology ; 67(3): 391-3, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23988558

RESUMO

The purpose of this work was to assess commercially available Cryotech Vitrification Kit, in terms of survival, in vitro development and pregnancy rate for bovine embryos. Cumulus-oocyte complexes (COCs) were recovered from ovaries obtained from slaughtered cows and then matured in vitro for 22 h. COCs were fertilized by sex-sorted sperm in IVF-mSOF and cultured in IVC-mSOF for 7 days to the blastocyst stage. Blastocysts were vitrified with the Cryotech Vitrification Kit(®) and then either warmed to check viability or transferred to synchronized heifers. We observed 100% survival of the in vitro produced blastocysts and obtained the same pregnancy rate (46.8%) as that obtained using fresh in vitro produced blastocysts. We thus conclude that the Cryotech vitrification method is a valid alternative to other vitrification or slow-cooling methods in the bovine species and that it is ready for livestock production.


Assuntos
Blastocisto/citologia , Bovinos/embriologia , Criopreservação/veterinária , Vitrificação , Animais , Sobrevivência Celular , Criopreservação/métodos , Transferência Embrionária/veterinária , Feminino , Fertilização in vitro/veterinária , Gravidez
3.
Reprod Domest Anim ; 48(4): 545-53, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23189959

RESUMO

Glycolytic and pentose phosphate pathway (PPP) activities were modulated in porcine cumulus-oocyte complexes (COCs) during in vitro maturation (IVM) by the addition of inhibitors or stimulators of key enzymes of the pathways to elucidate their relative participation in oocyte maturation. The activities of glycolysis and PPP were evaluated by lactate production per COC and by the brilliant cresyl blue test, respectively. Glucose uptake per COC and the oocyte maturation rate were also evaluated. Lactate production, glucose uptake and the percentage of oocytes reaching metaphase II decreased in a dose-dependent manner in the presence of the pharmacological (NaF) or the physiological (ATP) inhibitors of glycolysis (p < 0.05). The addition of the physiological stimulator of glycolysis (AMP) caused no effect on lactate production, glucose uptake or the meiotic maturation rate. The pharmacological (6-AN) and the physiological (NADPH) inhibitors of PPP induced a dose-dependent decrease in the percentage of oocytes with high PPP activity and in the nuclear maturation rate (p < 0.05). The physiological stimulator of PPP (NADP) caused no effect on the percentage of oocytes with high PPP activity. The glycolytic and PPP activities of porcine COCs and maturational competence of oocytes seem to be closely related events. This study shows for the first time the regulatory effect of ATP and NADPH as physiological inhibitors of glycolysis and PPP in porcine COCs, respectively. Besides, these pathways seem to reach their maximum activities in porcine COCs during IVM because no further increases were achieved by the presence of AMP or NADP.


Assuntos
Glicólise/fisiologia , Técnicas de Maturação in Vitro de Oócitos/métodos , Oócitos/crescimento & desenvolvimento , Via de Pentose Fosfato/fisiologia , Suínos , 6-Aminonicotinamida/farmacologia , Monofosfato de Adenosina/farmacologia , Trifosfato de Adenosina/farmacologia , Animais , Células Cultivadas , Células do Cúmulo , Feminino , Glucose/metabolismo , Glicólise/efeitos dos fármacos , Ácido Láctico/biossíntese , NADP/farmacologia , Oócitos/metabolismo , Via de Pentose Fosfato/efeitos dos fármacos , Fluoreto de Sódio/farmacologia
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