RESUMO Benzoato de estradiol (EB), cipionato de estradiol (EC) e hormônio liberador de gonadotrofinas (GnRH) foram avaliados como indutores da ovulação na IATF em vacas mestiças em lactação. No experimento I (n=45) a dinâmica folicular foi avaliada, enquanto no experimento II (n=171) a eficiência reprodutiva foi avaliada. Todas as fêmeas foram submetidas a um protocolo de sincronização: inserção no dia 0 (D0) de dispositivo intravaginal de liberação de progesterona (PRID; 1g) mais administração de EB 2mg; D8, remoção de PRID, administração de 0,150mg de PGF2α e 400 UI de eCG, e as vacas foram alocadas em três tratamentos: 1) TEB9 - administração IM de 1mg EB em D9 e AI realizada 52 horas após a remoção PRID; 2) TEC - administração IM de 1mg EC em D8 e AI realizada 48 horas após a remoção de PRID; e 3) TGnRH - administração de 100μg GnRH em D10 e AI realizada 52 horas após a remoção de PRID. A taxa de crescimento folicular foi menor no grupo EC (p <0,05). Não houve efeito dos tratamentos nas taxas de ovulação e prenhez (p >0,05). O uso de EB, EC e GnRH como indutores de ovulação em protocolos de IATF não mostrou diferenças marcantes nos padrões avaliados de dinâmica folicular e prenhez.

ABSTRACT Estradiol benzoate (EB), estradiol cypionate (EC), and gonadotrophin releasing hormone (GnRH) were evaluated as ovulation inducers for TAI of crossbred lactating cows. In experiment I (n = 45), the follicular dynamics was evaluated, while in experiment II (n = 171) the reproductive efficiency was evaluated. All females were submitted to a synchronization protocol: insertion on day 0 (D0) of intravaginal progesterone -release intravaginal device (PRID; 1g) plus administration of EB 2mg; D8, PRID removal, administration of 0.150mg PGF2α and 400 IU of eCG, and cows were allocated into three treatments: 1) TEB9 - IM administration of 1mg EB on D9 and AI performed 52 hours after PRID removal; 2) TEC - IM administration of 1mg EC on D8 and AI performed 48 hours after withdrawal of PRID; and 3) TGnRH - administration of 100pg GnRH on D10 and AI performed 52 hours after removal of PRID. The follicular growth rate was lower in the EC group (p <0.05). There was no effect of treatments on ovulation and pregnancy rates (p >0.05). The use of EB, EC, and GnRH as ovulation inducers in the TAI protocol did not show marked differences in the evaluated patterns of follicular dynamics and pregnancy.

O objetivo do trabalho foi avaliar o efeito da associação entre crioprotetores ainda pouco estudados no Brasil como a dimetilformamida e a trealose em meio diluidor, por meio de protocolos de descongelamento rápido e lento. Foram utilizados três cães machos, adultos, sadios da raça Labrador do Retrievier, que foram submetidos a uma coleta de sêmen semanal durante o período de cinco semanas. Os três meios diluentes utilizados neste estudo foram: (D1)-tris-citrato, acrescido de 3% de dimetilformamida + 3% de glicerol, (D2)-3% de dimetilformamida e de trealose e (D3)-4% de glicerol. No descongelamento, metade das amostras de cada meio diluente foi descongelada pelo método rápido, em banho-maria a 75ºC por sete segundos, seguido de nova imersão a 37 ºC por 1 minuto. A outra metade foi descongelada pelo método lento, em banho-maria à 37 ºC por 1 minuto. O sêmen foi avaliado quanto à motilidade progressiva, vigor espermáticos e integridade de membrana. Pra isso, as amostras foram submetidas aos testes hipo-osmótico e de integridade da membrana plasmática e do acrossoma (fluorescência). Os resultados indicam que o uso do glicerol como crioprotetor em diluidor TRIS proporciona maior eficácia na criopreservação dos espermatozoides da espécie canina, quando comparados com a dimetilformamida associada ao glicerol ou trealose.

The aim of this study was to evaluate the association between cryoprotectants little studied in Brazil such as dimethylformamide and trehalose amid thinner, using protocols of fast and slow defrosting. Three adult Labrador Retrievier male, healthy dogs, weekly submitted to one semen collection during five-weeks period, were used. The base diluent medium used in this study was tris-citrate added with 3% of dimethylformamide + 3% glycerol (D1), 3% dimethylformamide and trehalose (D2) and 4% glycerol (D3). At defrosting, half of the semen samples from each diluent medium was defrosted by rapid method in water-bath at 75 °C for seven minutes, followed by a new immersion at 37 °C for 1 minute. The other half of the samples was defrosted by slow method, in water-bath at 37 °C for 1 minute. The semen was evaluated for sperm progressive motility and vigor, besides membrane integrity. For this, the semen samples were submitted to either hyposmotic and membrane integrity tests of the plasmatic membrane and acrosome (fluorescence). The results indicated that the use of glycerol as cryoprotector in TRIS diluter provides greater efficacy in cryopreserving spermatozoa of the canine species, when compared to dimethylformamide associated with trehalose or glycerol.

The objective of this work was to evaluate the effects of protein and/or starch supplementation on the nutritional performance of cattle grazing on low-quality tropical forage. Five crossbred steers (Holstein × Gyr) with an average body weight (BW) of 397 kg that were fitted with ruminal and abomasal cannulae were used. The animals were kept in individual signal-grass (Bracharia decumbens) paddocks. Five treatments were evaluated: 1 - control (without supplementation); 2 - supplementation with 1 g of crude protein (CP) per kg of BW; 3 - supplementation with 2.5 g of starch per kg of BW; 4 - supplementation with CP and starch as described for treatments 2 and 3; and 5 - supplementation as described for treatment 4 but replacing the corn starch with a mixture of corn starch and nitrogenous compounds, thereby resulting in an energy supplement of 150 g CP/kg of dry matter. The experiment was performed according to a 5 × 5 Latin square design in a 2 × 2 + 1 factorial arrangement. The forage intake was not affected by any of the factors evaluated in this study. The production of microbial nitrogen in the rumen was not affected by nitrogen or starch supplementation. The apparent nitrogen balance was only increased when both starch and nitrogen were supplied. Supplementation with both starch and nitrogenous compounds for cattle grazing on low-quality tropical forage is characterized by an interactive metabolic effect that increases nitrogen accretion by the animals.

Objetivou-se avaliar os efeitos de compostos nitrogenados suplementares sobre o consumo, a digestibilidade e a síntese de proteína microbiana em bovinos alimentados com forragem tropical de baixa qualidade. Foram utilizadas cinco novilhas mestiças Holandês × Zebu, com peso vivo médio de 209 kg, fistuladas no rúmen. O volumoso consistiu de feno de capim-braquiária (Brachiaria decumbens Stapf.) (5,08% de proteína bruta (PB), com base na matéria seca), fornecido à vontade. Os cinco tratamentos avaliados foram definidos de acordo com o nível de suplementação proteica (0, 3, 5, 7 e 9 pontos percentuais acima do nível de PB da forragem). Como fonte de compostos nitrogenados, empregou-se mistura de ureia, sulfato de amônia e albumina, nas proporções de 4,5:0,5:1,0, respectivamente. O experimento constou de cinco períodos experimentais, segundo delineamento em quadrado latino 5 × 5. Os níveis médios de PB observados nas dietas foram de 5,28; 8,08; 9,82; 11,87 e 13,63%, com base na matéria seca (MS). Verificou-se efeito quadrático dos níveis de PB na dieta sobre os consumos de MS, matéria orgânica (MO) e fibra em detergente neutro (FDN) (kg/dia), com respostas máximas nos níveis de 10,83%, 10,78% e 10,37% de PB, respectivamente. Os coeficientes de digestibilidade da MO e FDN apresentaram relação do tipo linear-response-plateau com os níveis de PB na dieta com início de platô (resposta máxima) em 7,93 e 7,55% de PB, respectivamente. A concentração média diária de nitrogênio amoniacal ruminal apresentou comportamento linear crescente em função dos níveis de PB da dieta, com valor estimado de 15,33 mg/dL, equivalente ao máximo consumo de MS. A avaliação da relação entre consumo de nitrogênio e fluxo intestinal de nitrogênio microbiano indica que as estimativas dessas variáveis tornam-se equivalentes no nível de 7,13% de PB na dieta.

The objective of this study was to evaluate the effects of supplementation with nitrogenous compounds on intake, digestibility, and rumen microbial synthesis in cattle fed low-quality tropical forage. Five crossbred heifers, averaging 209 kg and fitted with ruminal fistulla, were used. The animals were fed ad libitum with signal grass (Brachiaria decumbens Stapf.) hay, which had crude protein (CP) content of 5.08%, as dry matter (DM) basis. The five treatments were defined according to the increasing level of CP in the diet (0, 3, 5, 7, and 9 percentile points above the forage CP level). The supplement consisted of the following nitrogen sources: urea, ammonium sulfate and albumin (4.5:0.5:1.0, respectively). The experiment was carried out according to a 5 × 5 Latin square design, with five experimental periods. The average CP levels in the diets were: 5.28, 8.08, 9.82, 11.87, and 13.63% on DM basis. The intakes of DM, organic matter (OM), and neutral detergent fiber (NDF) showed a quadratic response according to CP levels in the diet, with maximum responses at 10.83%, 10.78%, and 10.37% CP, respectively. The digestibility coefficients of OM and NDF showed a linear-response-plateau response according to CP levels, with the plateau beginning (maximum response) at 7.93% and 7.55% CP, respectively. The average daily concentration of rumen ammonia nitrogen (RAN) was positively related with CP levels. The RAN estimate associated with the maximum DM intake was 15.33 mg/dL. It was observed that intestinal flow of microbial nitrogenous compounds and nitrogen intake became equivalent to each other at 7.13% of CP.

O objetivo neste trabalho foi avaliar os efeitos da dimetil-formamida na criopreservação de sêmen caprino, por meio de testes in vitro. As partidas de sêmen foram congeladas com os diluidores leite desnatado-gema, associado a diferentes crioprotetores e concentrações: 7% de glicerol (T1); 3,5% de glicerol e 3,5% de dimetil-formamida (T2) e 5% de dimetil-formamida (T3). O sêmen foi centrifugado e envasado em palhetas de 0,5 mL, sendo resfriado por 40 minutos, atingindo 5,0°C e permanecendo nesta temperatura por mais 1 hora e 20 minutos. Os parâmetros avaliados in vitro foram a motilidade progressiva e o vigor espermático, a integridade acrossômica, a integridade da membrana plasmática (HO) e a reação acrossômica. Observou-se perda de 30,0% da motilidade inicial quando as amostras foram submetidas aos procedimentos de criopreservação. A perda de integridade da membrana plasmática, avaliada pelo teste hiposmótico (HO) foi de 19%. As lesões de acrossoma aumentaram em 3% durante o teste de termo-resistência (TTR) lento. Não houve diferença entre os tratamentos quanto aos aspectos de motilidade nos tempos de 0,00; 0,05; e 1,00 horas do TTR e vigor em todos os tempos. No tempo de 2,00 horas do TTR, registrou-se diferença entre os tratamentos 1 e 2, de modo que a motilidade no tratamento 2 foi superior às demais. Os valores de integridade de membrana plasmática, integridade acrossômica e reação acrossômica pós-descongelamento não diferiram entre os tratamentos, indicando que a dimetil-formamida não foi superior ao glicerol na manutenção da qualidade espermática após a criopreservação.

The objective of this trial was to evaluate the efficiency of dimethylformamide on cryopreservation of goat semen using semen physical analyses and complementary tests. Alpine and Saanen bucks from the Dairy Goat Experimental Station- DZO were used. Semen samples were frozen with a yolk-skimmed milk diluent and cryoprotectors with different concentrations as follows: 7% glycerol (T1), 3.5% glycerol plus 3.5% dimethylformamide (T2) or 5% dimethylformamide (T3). Semen was centrifuged, diluted, and bottled in 0.5 mL straws followed by cooling for 40 minutes until reach 5.0°C and kept at this temperature for additional 80 minutes. Samples were then exposed to liquid nitrogen vapor for 15 minutes and finally frozen. Thawing was done in a waterbath at 37°C for 50 seconds. The following variables were evaluated in vitro: sperm progressive motility and vigor, acrosomal integrity and reaction, and plasmatic membrane integrity. The cryopreservation procedures reduced 30.0% of the initial motility and 19% of plasmatic membrane integrity that was evaluated using the hyposmotic swelling test (HOST). It was observed an increaseof 3% in acrosomal lesions when samples were submitted to a slow thermoresistance test (TRT). No significant differences in sperm motility were observed among treatments at 0, 5, and 60 minutes of TRT as well as in sperm vigor at all TRT times. However, at 120 minutes of TRT a significant difference in sperm motility was found comparing T1 and T2 while T3 was intermediate. There were no significant differences on plasmatic membrane integrity, acrosomal integrity, and post-thawing acrossomal reaction across treatments. It can be concluded that dimethylformamide can be a viable alternative for goat semen cryopreservation used alone or in association with glycerol.