Long-term characteristics of idiopathic persistent corpus luteum in the mare.

Persistent CL (PCL; n = 10) in mares was studied daily from Day 20 (Day 0 = ovulation) to the ending ovulation. In addition, the 10 days before ovulation at the end of a PCL were compared with the end of an interovulatory interval (IOI; n = 28) during the same months. Concentration of P4, cross-sectional area of CL, and percentage of CL with Doppler signals of blood flow during PCLs remained constant from 64 to about 33 days before the end of luteolysis and then decreased linearly. Concentration of LH between Day 20 and beginning of the ovulatory LH surge increased linearly. A dominant follicle developed on average every 15 days throughout each PCL. Novel transient P4 depressions were detected with the P4 nadir at a day of maximal diameter of a dominant follicle. At the apparent beginning of luteolysis before the ending ovulation, P4 concentration in PCLs (5.0 ± 0.5 ng/mL) was less (P < 0.0001) than that in IOIs (9.3 ± 0.6 ng/mL). Concentration of LH began to increase 2 days before the end of luteolysis in each group, but concentration on the day of the ending ovulation in PCLs (3.7 ± 0.3 ng/mL) was less (P < 0.005) than that in IOIs (8.9 ± 1.8 ng/mL). In a separate survey of PCLs (n = 23) and IOIs (n = 352), frequency of PCL (6.1%) differed significantly among mares indicating repeatability. These original and critical comparisons between PCLs and IOIs should provide hypotheses for further study.

Ultrastructural characterization of in vivo-produced ovine morulae and blastocysts.

The ultrastructure of in vivo-produced ovine embryos, at the morula, early blastocyst and late blastocyst stages, was evaluated using transmission electron microscopy. Embryonic cells were characterized by the presence of intact intercellular junctions, numerous mitochondria, smooth endoplasmic reticulum cisternae and light vesicles. Polyribosomes, rough endoplasmic reticulum cisternae, secondary lysosomes, Golgi complexes and lipid droplets were also observed in the cytoplasm. The nucleus was well defined and organized, with an intact envelope rich in nuclear pore complexes, and one or more reticular nucleoli. Microvilli were present in external blastomeres of morulae and became more abundant in trophectoderm cells of early and late blastocysts. Light vesicles seemed to be associated with small cisternae of Golgi and endoplasmic reticulum origin. These cisternae fused and created light vesicles with engulfed heterogeneous cytosolic structures, small cisternae and vesicles. Their labile membrane enabled them to rapidly coalesce into medium-sized vesicles that began to engulf mitochondria and lipid droplets, forming giant vacuoles mostly filled with fat. Incomplete matured secretory vesicles were observed to exocytose into the perivitelline space of morulae, whereas fully matured secretory vesicles appeared only in trophectoderm cells, being exocytosed into the blastocoelic cavity. These observations suggested that these endoplasmic-/Golgi-derived vesicles behave as active autophagic organelles presenting probably a maturation process from compact morulae to blastocyst.

Ultrastructural characterization of fresh and cryopreserved in vivo produced ovine embryos.

Controlled slow freezing and vitrification have been successfully used for ovine embryo cryopreservation. Selection of embryos for transfer is based on stereomicroscopical embryo scoring after thawing, but the subjectivity inherent to this selection step has been demonstrated by ultrastructural studies of controlled slow frozen, in vivo produced ovine morulae and blastocysts. These studies have shown that certain abnormalities remain undetected by stereomicroscopy only. In the present study, using ovine in vivo produced morulae and blastocysts, we have studied the ultrastructural alterations induced by open pulled straw vitrification (OPS) and controlled slow freezing, compared stereomicroscopical embryo scoring with light microscopy evaluation of embryo's semithin sections, and related the ultrastructural cellular damage with the embryo classification by stereomicroscopical embryo scoring of embryos' and semithin section evaluation by light microscopy. The ultrastructural lesions found for OPS-vitrified and controlled slow frozen embryos were similar, independently of embryo stage. A significant higher number of grade 3 embryos was found at stereomicroscopical scoring after controlled slow freezing (P=0.02), and a significant higher number of grade 3 blastocysts was found at semithin sectioning after OPS vitrification (P=0.037). The extension of ultrastructural damage, especially of mitochondria and cytoskeleton, was related to the semithin classification but not to stereomicroscopical scoring at thawing. This suggests that semithin scoring is a useful tool for predicting ultrastructural lesions and new improvements in cryopreservation and thawing methods of ovine embryos are still warranted, including in the case of blastocysts cryopreserved by OPS vitrification.