ABSTRACT
The present work was designed to study the in vitro and in vivo viability, as assessed by blastocyst formation, pregnancy rate and term delivery of bovine embryos produced under completely defined conditions with or without insulin-like growth factor I (IGF-I) following direct transfer after cryopreservation. Slaughterhouse-derived bovine oocytes were matured for 24h, fertilized with frozen-thawed spermatozoa and cultured in vitro under completely defined conditions with or without exposure to IGF-I (5 ng/ml). Only those embryos classified as excellent or good quality blastocysts were frozen. Each blastocyst was individually loaded into a straw, seeded and pre-cooled to -7 degrees C. After 10 min at -7 degrees C straws were frozen further to -30 degrees C at a rate of 0.3 degrees C/min and then plunged into liquid nitrogen. Synchronized recipient cows received one embryo in the horn ipsilateral to the corpus luteum (CL). Pregnancies were diagnosed by ultrasonography 35-45 days after embryo transfer (ET). IGF-I failed to improve cleavage rate, as well as blastocyst production, when added during in vitro culture (IVC). Pregnancy outcome was not significantly improved in cows that received an IGF-I-treated embryo compared with controls (4/10 versus 3/10, respectively). Five out of six calves delivered to date were born alive and healthy. We have shown that it is possible to obtain healthy live offspring from frozen-thawed embryos produced under chemically defined conditions after direct transfer.
Subject(s)
Cattle/physiology , Cryopreservation/veterinary , Embryo Transfer/veterinary , Fertilization in Vitro/veterinary , Insulin-Like Growth Factor I/pharmacology , Pregnancy Outcome/veterinary , Animals , Blastocyst/physiology , Cattle/embryology , Cell Division/drug effects , Culture Media , Female , Fertilization in Vitro/methods , Pregnancy , Pregnancy RateABSTRACT
In a series of 3 experiments, participants learned visual patterns that contained the same number of visual features but varied in the complexity of the interrelations among the features. The results indicate a large and orderly effect of the pattern's syntactic complexity on recognition speed. Evidence is provided that this effect was not due to physical characteristics, target-foil similarity, speed-accuracy trade-off, or level of pattern learning. A multiple-encoding explanation of the effect is described. According to this framework, there is an initial, automatically generated encoding of the pattern as a short-term pictorial representation that becomes the basis for the construction of a second syntactic-propositional encoding. In this model, the participant's "sense of familiarity" for a particular stimulus is associated only with the syntactic-propositional encoding.
Subject(s)
Attention , Discrimination Learning , Mental Recall , Pattern Recognition, Visual , Adult , Female , Humans , Male , Orientation , Paired-Associate Learning , Reaction TimeABSTRACT
Two hundred forty excellent-quality blastocysts flushed from 53 superovulated Holstein heifers were frozen by 1 of 16 procedures in a 2 x 2 x 2 x 2 factorial design. The main effects included a simple, inexpensive, portable mechanical freezing unit instead of a programmable Liquid Nitrogen (LN) freezer for freezing bovine embryos, cryoprotective agents dimethyl sulfoxide (DMSO) and glycerol, addition rates of the cryoprotectants and freezing rates. Embryo viability was assessed morphologically and by fluorescein diacetate (FDA) evaluation. Neither the type of freezer, the cryoprotectant nor the rate of cryoprotectant addition affected embryo viability. Embryo survival after 12 h of incubation was higher (P < 0.05) using a conventional freezing rate than a two-step method (37.2 vs 16.5%). The correlation coefficient between viability evaluation methods (morphology vs FDA) was influenced by cryoprotectant and embryo processing methods and ranged from -0.13 to +0.70. This study indicates that more simplified embryo freezing equipment and handling procedures may provide protection equal to that of more complicated, expensive equipment and more time-consuming methods. Economical on-farm embryo freezing is feasible.