The effect of superovulatory treatment during the two phases of the ovarian cycleon follicular growth and embryo quality was evaluated in 45 sexually adult llamas. Animals bearing a >7 mm follicle, observed by ultrasonography, were selected and allocated into 3 groups: T0 (non-stimulated), T1 (superovulatory treatment during the non luteal phase), and T2 (superovulatory treatment during the luteal phase). Animals in groups T1 and T2 received 1 ml of LH (day 0) for synchronization of the follicular wave and 1000 IU of eCG (day 3) as superovulatory treatment. Vaginal sponges impregnated with progesterone were used on days 3 to 7 in T2 to simulate the luteal phase. The induction of the ovulation (day 8) was done through natural mating and the application of GnRH (1 ml). Embryo recovery was done 7 days after natural mating (day 15) on T1 and T2. Similarly, embryo recovery was done 7 days ...

Se evaluó el efecto del tratamiento superovulatorio en las dos fases del ciclo ovárico sobre la respuesta folicular y la calidad embrionaria en 45 llamas hembras adultas. Se incluyeron en el estudio aquellos animales que a la ecografía presentaron un folículo preovulatorio >7 mm. Los animales se distribuyeron en tres grupos: T0 (no estimulado), T1 (tratamiento superovulatorio en fase no luteal) y T2 (tratamiento superovulatorio en fase luteal). Los animales de T1 y T2 recibieron 1 ml de LH (día 0) para sincronizar la onda folicular y 1000 UI de eCG (día 3) como tratamiento superovulatorio. Se utilizaron esponjas vaginales impregnadas con progesterona entre el día 3 y 7 para simular la fase luteal en el T2. La inducción de la ovulación se hizo mediante monta natural y aplicación de 1 ml de GnRH (día 8). La colección y evaluación de embriones se realizó 7 días post cópul...

Semen was collected in a Spectacled Bear (Tremarctos ornatus) reared in captivity using the electroejaculation technique. Four series of 6 volt discharges by 15 seconds each plus manual stimulation were carried out. An effective penis erection and small volume of ejaculate was obtained in the last series of electrical stimulus. Seminal motility was 50%. Further studies are required to optimize the use of the electroejaculator in order to obtain higher volumes and better semen quality.

The aim of this study was to determine the optimal concentration of glycerol, ethylene glycol and dimethyl sulfoxide (DMSO) in the cryopreservation of epididymal spermatozoa of alpaca. The effect of different concentrations of glycerol, ethylene glycol and DMSO: T1 (0 M), T2 (0.25 M), T3 (0.5 M), T4 (0.75 M), T5 (1 M), T6 (1.25 M), T7 (1.5 M) and T8 (1.75 M) was evaluated. A polynomial regression model was used to determine the best concentration of each cryoprotectant, resulting 1.16, 1.02 and 0.9 M the optimal concentrations for glycerol, ethylene glycol and DMSO respectively. In Experiment 2, the effect of the optimal concentrations between glycerol, ethylene glycol and DMSO on motility, plasma membrane integrity, and acrosomal viability and integrity in alpaca epididymal spermatozoa were analyzed. The results showed a mean of 35.8, 51.8 and 38.3% for DMSO and 30.8, 45.0 and 33.8% for...

Semen was collected in a Spectacled Bear (Tremarctos ornatus) reared in captivity using the electroejaculation technique. Four series of 6 volt discharges by 15 seconds each plus manual stimulation were carried out. An effective penis erection and small volume of ejaculate was obtained in the last series of electrical stimulus. Seminal motility was 50%. Further studies are required to optimize the use of the electroejaculator in order to obtain higher volumes and better semen quality.

The aim of this study was to determine the optimal concentration of glycerol, ethylene glycol and dimethyl sulfoxide (DMSO) in the cryopreservation of epididymal spermatozoa of alpaca. The effect of different concentrations of glycerol, ethylene glycol and DMSO: T1 (0 M), T2 (0.25 M), T3 (0.5 M), T4 (0.75 M), T5 (1 M), T6 (1.25 M), T7 (1.5 M) and T8 (1.75 M) was evaluated. A polynomial regression model was used to determine the best concentration of each cryoprotectant, resulting 1.16, 1.02 and 0.9 M the optimal concentrations for glycerol, ethylene glycol and DMSO respectively. In Experiment 2, the effect of the optimal concentrations between glycerol, ethylene glycol and DMSO on motility, plasma membrane integrity, and acrosomal viability and integrity in alpaca epididymal spermatozoa were analyzed. The results showed a mean of 35.8, 51.8 and 38.3% for DMSO and 30.8, 45.0 and 33.8% for...

The study aimed to evaluate the superovulatory response and conception rate byapplying the technique of non-surgical embryo transfer in dairy cows of a commercialfarm in the Lima milkshed. Eight donor cows were used and distributed in two workingyears. Donors were synchronized with estrogens, progestagens and luteolitic agents,superovulated with 400 mg of FSH, and inseminated with two doses of frozen semen. Therecipient animals (n=28) were also distributed in two years. The Pre-synch protocol wasused for estrus synchronization in the first year and the CIDR-synch protocol in thesecond year. The expected day of heat presentation coincided for both donors andrecipients. The recovery of embryos was done seven days post service where embryoswere classified and immediately transferred. Pregnancy diagnosis by transrectalultrasonography was done at day 28 post transfer. A total of 23 embryos we...

El estudio tuvo como objetivo evaluar la respuesta superovulatoria y la tasa de concepción al aplicar la técnica no quirúrgica de transferencia de embriones en vacas lecheras de un establo comercial de la cuenca de Lima. Se utilizaron ocho vacas donadoras, distribuidas en dos años de trabajo. Estas fueron sincronizadas con estrógenos, progestágenos y agentes luteolíticos, superovuladas con 400 mg de FSHe inseminadas con dos dosis de semen congelado. Se utilizaron 28 receptoras, también distribuidas en dos años. En el primer año se sincronizaron con el protocolo Pre-synchy en el segundo año con el protocolo CIDR-synch. Se hizo coincidir el día esperado del celo de las donadoras y receptoras. Los embriones fueron recolectados en el día siete del servicio, se clasificaron y se transfirieron de inmediato a las receptoras. Eldiagnóstico de gestación se realizó mediante ultraso...

DNA integrity in alpaca spermatozoa was evaluated by flow cytometric analysis in sperm cryopreserved using antioxidants analogues of superoxide dismutase (Tempo and Tempol). Twelve alpaca semen samples were frozen using an extender based on skim milk, fructose, egg yolk, and ethylene glicol. Each sample was divided into three aliquots: Control group, Tempo group (1 mM), and Tempol group (1 mM). Antioxidants were added during cooling at 10 °C. After thawing, samples were fixed using 2% formaldehyde solution and permeabilizated using 0.8% Triton X-100 solution. TUNEL assay and Iodure propidium (PI) were used for evaluation of DNA integrity and cell permeability. Spermatozoa labeled with TUNEL and PI was classified as cells with DNA damaged. Samples were analyzed by flow cytometric using a 488 nm laser, counting at least 10 000 cells per sample, and by epifluorescene microscopy. Frequency ...

Se evaluó la estabilidad del ADN en espermatozoides de alpaca mediante citometría de flujo en muestras congeladas con antioxidantes análogos de superóxido dismutasa (Tempo y Tempol). Doce muestras de semen de alpaca fueron congeladas utilizando un dilutor en base a leche descremada, fructosa, yema de huevo y etilenglicol. Cada muestra fue dividida en tres porciones: grupo control, grupo Tempo (1 mM) y grupo Tempol (1 mM). Los antioxidantes fueron agregados al dilutor durante la curva de enfriamiento (10 °C). Las muestras fueron descongeladas y fijadas en una solución de formaldehido al 2% y permeabilizadas utilizando una solución de Triton X-100 al 0.8%. La integridad del ADN espermático se evaluó con la técnica de TUNEL y una sonda fluorescente para determinar la viabilidad celular (Ioduro de propidio [PI]). Los espermatozoides marcados con la sonda del TUNEL y PI fueron consi...

The objective of this study was to evaluate the effect of three semen extenders (skim milk, Tris, and Tes) on cryopreservation of epididymal alpaca sperm. Previously, the effect of timespan since slaughtering or castration to the recovery of epididymal sperm was evaluated. Twenty-four alpaca testicles were used to obtain sperm from the epididymis in a buffered saline solution (PBS). The recovery of spermatozoa was performed at 0, 35, 48, and 72 hours (6 testes per group) after slaughtering or castration. Sperm motility, concentration, and sperm membrane functional integrity were analyzed. Sperm recovered after 35 hours was not usable for cryopreservation. Sperm samples recovered at 0 hours were subjected to the process of freezing. Samples were diluted with skim milk, Tris, and Tes, cooled from 35 to 5 °C in 90 minutes, packed into 0.25 ml straws and frozen in liquid nitrogen. After tha...

El estudio tuvo por objetivo evaluar el efecto de tres dilutores (Tris, Tes y leche descremada) en la criopreservación de espermatozoides obtenidos del epidídimo de alpaca. Previamente se determinó el efecto del tiempo entre el beneficio/castración y la recuperación de los espermatozoides del epidídimo. Se utilizaron 24 testículos de alpacas para la obtención de los espermatozoides directamente del epidídimo en una solución fisiológica buferada (PBS). La recuperación de espermatozoides se realizó a las 0, 35, 48 y 72 horas (6 testículos por grupo) y se evaluó la motilidad, concentración espermática e integridad funcional de membrana. Los espermatozoides recuperados a partir de 35 horas post beneficio/castración no fueron aptos para ser congelados. Las muestras recuperadas a las 0 horas fueron diluidas con Tris, Tes y leche descremada, enfriadas desde 35 a 5 oC en 90 min...