ABSTRACT
The domestic geese used in this experiment were free-living, from a lake located in an urban area and its population had increased dramatically. The need for a project proposing the sterilization of some males to restrain population growth, led to the need for sexing these animals. As domestic geese present minimal sexual dimorphism, two techniques were tested: cytogenetic analysis and post anesthetic inspection of the cloaca. There were used eight adults geese randomly chosen from a group of 80 animals. They were caught with nets or by hand, were individually transported and housed in appropriate place waiting for the cytogenetic analysis (three to four days). For the chromosomal sexing, was collected 2 mL of blood and the peripheral blood lymphocyte culture technique was used. The sample was treated with hypotonic KCl, fixed in three changes of methanol/acetic acid solution. The slides were prepared with the standard technique and examined under an optical microscope to observe the metaphase. To the technique of cloaca eversion, was performed injectable anesthesia with tiletamine-zolazepam 5%. Ten minutes after anesthesia, the cloaca has been everted to visualize the internal structures and sex determination. The techniques were performed in blinded trial to avoidinaccurate results. From the eight animals submitted to chromosomal sexing technique, five were identified as male and three as females, reaching 100% agreement when compared with the cloaca eversion technique. Sexing chromosomal technique appeared to cause the least discomfort in the animals evaluated, proving to be a reliable technique for sexualdetermination and favorable to animal welfare. (AU)
Os gansos domésticos utilizados neste experimento eram de vida livre, pertencentes a um lago localizado em uma área urbana e sua população havia aumentado dramaticamente. A necessidade de um projeto com foco na esterilização de alguns machos, para reduzir o crescimento populacional, levou à necessidade de sexagem desses animais. como os gansos domésticos apresentam mínimo dimorfismo sexual, duas técnicas foram testadas: análise citogenética e inspeção da cloaca pós-anestesia. Foram utilizados oito gansos adultos, escolhidos aleatoriamente de um grupo de 80 animais. Eles foram capturados com redes ou manualmente, transportados individualmente e alojados em local apropriado a espera da análise citogenética (três a quatro dias). Para a sexagem cromossomal, foram coletados 2 ml de sangue e a técnica de cultura de linfócitos periféricos foi empregada. As amostras resultantes foram tratadas com kcl hipotônico, fixadas em três trocas de solução de metanol e ácido acético. As lâminas foram preparadas com a técnica padrão e examinadas ao microscópio óptico para observação das metáfases. para a técnica de eversão da cloaca, foi realizada a anestesia injetável com tiletamina-zolazepam 5%. Dez minutos após a anestesia, a cloaca foi evertida para a visualização das estruturas internas e a determinação sexual. AAs técnicas foram conduzidas em duplo cego, para melhor acurácia dos resultados. Dos oito animais submetidos à técnica de sexagem cromossomal, cinco foram identificados como machos e três como fêmeas, alcançando 100% de concordância quando comparada com a técnica de eversão da cloaca. A técnica de sexagem cromossomal aparentou causar o menor desconforto nos animais avaliados, mostrando-se uma técnicaconfiável para determinação sexual e favorável ao bem-estar animal. (AU)
Subject(s)
Animals , Geese/genetics , Karyotype , Cloaca , Cytogenetic Analysis/veterinary , Sex Determination Analysis/veterinary , Anesthesia/veterinaryABSTRACT
Os gansos domésticos utilizados neste experimento eram de vida livre, pertencentes a um lago localizado em uma área urbana e sua população havia aumentado dramaticamente. a necessidade de um projeto com foco na esterilização de alguns machos, para reduzir o crescimento populacional, levou à necessidade de sexagem desses animais. como os gansos domésticos apresentam mínimo dimorfismo sexual, duas técnicas foram testadas: análise citogenética e inspeção da cloaca pós-anestesia. foram utilizados oito gansos adultos, escolhidos aleatoriamente de um grupo de 80 animais. eles foram capturados com redes ou manualmente, transportados individualmente e alojados em local apropriado a espera da análise citogenética (três a quatro dias). para a sexagem cromossomal, foram coletados 2 ml de sangue e a técnica de cultura de linfócitos periféricos foi empregada. as amostras resultantes foram tratadas com kcl hipotônico, fixadas em três trocas de solução de metanol e ácido acético. as lâminas foram preparadas com a técnica padrão e examinadas ao microscópio óptico para observação das metáfases. para a técnica de eversão da cloaca, foi realizada a anestesia injetável com tiletamina-zolazepam 5%. dez minutos após a anestesia, a cloaca foi evertida para a visualização das estruturas internas e a determinação sexual. As técnicas foram conduzidas em duplo cego, para melhor acurácia dos resultados. D
ABSTRACT
The domestic geese used in this experiment were free-living, from a lake located in an urban area and its population had increased dramatically. The need for a project proposing the sterilization of some males to restrain population growth, led to the need for sexing these animals. As domestic geese present minimal sexual dimorphism, two techniques were tested: cytogenetic analysis and post anesthetic inspection of the cloaca. There were used eight adults geese randomly chosen from a group of 80 animals. They were caught with nets or by hand, were individually transported and housed in appropriate place waiting for the cytogenetic analysis (three to four days). For the chromosomal sexing, was collected 2 mL of blood and the peripheral blood lymphocyte culture technique was used. The sample was treated with hypotonic KCl, fixed in three changes of methanol/acetic acid solution. The slides were prepared with the standard technique and examined under an optical microscope to observe the metaphase. To the technique of cloaca eversion, was performed injectable anesthesia with tiletamine-zolazepam 5%. Ten minutes after anesthesia, the cloaca has been everted to visualize the internal structures and sex determination. The techniques were performed in blinded trial to avoidinaccurate results. From the eight animals submitted to chromosomal sexing technique, five were identified as male and three as females, reaching 100% agreement when compared with the cloaca eversion technique. Sexing chromosomal technique appeared to cause the least discomfort in the animals evaluated, proving to be a reliable technique for sexualdetermination and favorable to animal welfare.
Os gansos domésticos utilizados neste experimento eram de vida livre, pertencentes a um lago localizado em uma área urbana e sua população havia aumentado dramaticamente. A necessidade de um projeto com foco na esterilização de alguns machos, para reduzir o crescimento populacional, levou à necessidade de sexagem desses animais. como os gansos domésticos apresentam mínimo dimorfismo sexual, duas técnicas foram testadas: análise citogenética e inspeção da cloaca pós-anestesia. Foram utilizados oito gansos adultos, escolhidos aleatoriamente de um grupo de 80 animais. Eles foram capturados com redes ou manualmente, transportados individualmente e alojados em local apropriado a espera da análise citogenética (três a quatro dias). Para a sexagem cromossomal, foram coletados 2 ml de sangue e a técnica de cultura de linfócitos periféricos foi empregada. As amostras resultantes foram tratadas com kcl hipotônico, fixadas em três trocas de solução de metanol e ácido acético. As lâminas foram preparadas com a técnica padrão e examinadas ao microscópio óptico para observação das metáfases. para a técnica de eversão da cloaca, foi realizada a anestesia injetável com tiletamina-zolazepam 5%. Dez minutos após a anestesia, a cloaca foi evertida para a visualização das estruturas internas e a determinação sexual. AAs técnicas foram conduzidas em duplo cego, para melhor acurácia dos resultados. Dos oito animais submetidos à técnica de sexagem cromossomal, cinco foram identificados como machos e três como fêmeas, alcançando 100% de concordância quando comparada com a técnica de eversão da cloaca. A técnica de sexagem cromossomal aparentou causar o menor desconforto nos animais avaliados, mostrando-se uma técnicaconfiável para determinação sexual e favorável ao bem-estar animal.
Subject(s)
Animals , Karyotype , Cloaca , Geese/genetics , Anesthesia/veterinary , Cytogenetic Analysis/veterinary , Sex Determination Analysis/veterinaryABSTRACT
Oocytes from preantral follicles could be an alternative for in vitro maturation because most follicles are at the preantral stage. There are few studies that have sought to estimate the number of preantral follicles in bitches. Therefore, the aims of this study were to estimate the population of preantral follicles in the ovaries of small- and medium-sized prepubertal and adult bitches and compare the population of preantral follicles between the right and left ovaries and evaluate the frequency of multioocyte follicles (MOF). Eighty ovaries were collected by elective ovariohysterectomy from 40 healthy bitches. The bitches were divided into four groups: small-size prepubertal bitches (<10 kg, n = 20), medium-size prepubertal bitches (10-20 kg, n = 20), small-size adult bitches (<10 kg, n = 20), and medium-size adult bitches (10-20 kg, n = 20). Immediately after surgery, the ovaries were fixed in Bouin's solution and processed for histology. For each specimen, 70 histologic sections were cut and mounted on slides; then, the number of preantral follicles was estimated using a correction factor. The preantral follicles were classified according to the developmental stage. The data were analyzed using the Kruskal-Wallis test followed by Dunn's test for comparison between groups, and Fisher's exact test was used to evaluate the frequency of MOF (P ≤ 0.05). Considering the population of preantral follicles from the pair of ovaries, medium-size prepubertal bitches had the highest (P < 0.05) population of preantral follicles compared with the small and medium-size adult groups. There was a large variation in the numbers of preantral follicles among individuals of the same weight and within each group. There were differences between medium-size prepubertal and adult bitches regarding the population of preantral follicles in the right ovaries (145,482 ± 110,712 vs. 49,500 ± 44,821; P = 0.02); however, no differences were observed between the groups on the basis of comparisons of the number of preantral follicles in the left ovaries (P > 0.05). The prevalence of primordial MOF was higher in prepubertal bitches (47% vs. 28%), whereas adult bitches had a higher frequency of secondary MOF (49% vs. 25%; P < 0.05). We conclude that medium-size prepubertal bitches had the highest population of preantral follicles compared with small and medium-size adult bitches, and the use of only one ovary per bitch implied contrasting result. The presence of primordial MOF was higher in prepubertal bitches and at the secondary stage in adult bitches.
Subject(s)
Dogs/physiology , Ovarian Follicle/physiology , Sexual Maturation/physiology , Animals , Body Size/physiology , FemaleABSTRACT
The collection of epididymal sperm is an option for preservation of germplasm of genetically superior animals that need to be orchiectomized or have died. The extender type used to freeze sperm is important to avoid spermatozoal membrane damage and to preserve semen quality after cryopreservation. The objective of this study was to verify the effects of a commercial bovine extender (Bovimix(®); Nutricell, Campinas) and a traditional TRIS-citric acid-glucose-egg yolk-7% glycerol extender on cryopreservation of canine epididymal sperm. The testes of 13 adult dogs were kept at 5 °C for 24 h in saline solution, and epididymal sperm was recovered in Ringers solution without lactate and were evaluated for motility. Samples with ≥ 80% motility were pooled and then divided before dilution and packaging in 0.5 ml plastic straws, equilibration at 4 °C for 1 h, freezing in nitrogen vapour for 20 min and storing at -196 °C. The straws were thawed at 56 °C for 10 s and were evaluated for motility by computer assisted analysis (CASA). The semen parameters, sperm movement index, linearity, total motility and rapid progressive motility were statistically higher in Bovimix(®) than TRIS. In contrast, amplitude of lateral head displacement, slow sperm and static sperm were lower in Bovimix(®). Despite the high percentage of sperm defects in epididymal cells, regardless of the extender, we concluded that Bovimix(®) is a viable alternative for the freezing of canine epididymal sperm.