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Objective: The cardioprotective enzyme paraoxonase‐1 (PON1) suffers an important influence from genetic polymorphisms and nutritional factors. The aim of this study was to investigate the influence of diet, nutritional status, and the C(‐107)T polymorphism on PON1 arylesterase activity in children. Methods: This was a cross‐sectional study with 97 children, aged between 5 and 8 years, of both genders, from a pediatric outpatient clinic in southern Brazil. A sociodemographic, behavioral, and food consumption questionnaire was applied, and anthropometric measurements and laboratory blood samples were taken. PON1 arylesterase activity was measured by phenol extinction (U/mL), and DNA extraction and analysis of the PON1 C(‐107)T polymorphism were performed. The Hardy–Weinberg equilibrium was tested with the chi‐squared test and linear regression was used to estimate PON1 activity according to four adjustment models, with an acceptable error of 5%. Results: In the sample, the male gender accounted for 50.5%, 39.2% were 6 years of age, 54.5% had normal weight, and 51.5% had PON1 activity below the median (90.0, 15–30 U/mL). Genotype frequency was 54.6% (53/97), 31.0% (30/97), and 14.4% (14/97), respectively, for CT, CC, and TT, consistent with the Hardy–Weinberg equilibrium (p = 0.22). In the regression analysis, the model that included sociodemographic variables as well as frequency of consumption of fruits, vegetables, legumes, dairy products, and beans estimated a variability of 14.8% in PON1 activity combined with the PON1 C(‐107)T polymorphism. Conclusions: During childhood, a good‐quality diet with greater inclusion of healthy foods was important to predict the activity of the cardioprotective enzyme PON1 combined with the C(‐107)T polymorphism of the PON1 gene. Resumo: Objetivo: A enzima cardioprotetora Paraoxonase 1 (PON1) sofre importante influência de polimorfismos genéticos e fatores nutricionais. O objetivo deste estudo foi investigar a influência da alimentação, do estado nutricional e do polimorfismo C(‐107)T sobre a atividade arilesterase da PON1 em crianças. Métodos: Estudo transversal com 97 crianças entre 5 e 8 anos, de ambos os sexos, de um ambulatório de pediatria no sul do Brasil. Realizou-se questionário sociodemográfico, de comportamento e de consumo alimentar, medidas antropométricas e coleta de sangue em laboratório. A atividade arilesterase da PON1 foi mensurada pela extinção de fenol (U/mL), realizada extração do DNA e análise do polimorfismo PON1 C(‐107)T. O equilíbrio de Hardy‐Weinberg foi testado com qui‐quadrado e usada regressão linear para estimar a atividade da PON1 segundo quatro modelos de ajuste, erro aceitável de 5%. Resultados: Na amostra o sexo masculino representou 50,5%, 39,2% tinham 6 anos, 54,5% eram eutróficos e 51,5% tinha atividade da PON1 inferior à mediana (90,0;15‐30 U/ml). A frequência dos genótipos foi 54,6% (53/97), 31,0% (30/97) e 14,4% (14/97), respectivamente, para CT, CC e TT, estiveram em equilíbrio de Hardy‐Weinberg (p = 0,22). Na análise de regressão o modelo que incluiu variáveis sociodemográficas, de frequência do consumo de frutas, verduras, legumes, laticínios e feijões estimou uma variabilidade de 14,8% na atividade da PON1 combinada ao polimorfismo PON1 C(‐107)T. Conclusões: Na infância uma alimentação de boa qualidade, com maior participação de alimentos saudáveis foi importante para predizer a atividade da enzima cardioprotetora PON1 combinada ao polimorfismo C(‐107)T do gene da PON1.

The objective of this study was to determine the ability of prostaglandin E2 (PGE2) to induce ovulation and expression of PGE2 receptor (EP2 and EP4) and COX genes (COX-1 and COX-2) in the ovary and pituitary of prepubertal mice. The positive control consisted of the application of 5 μg of gonadotropin-releasing hormone (GnRH, n = 29); the negative control applied 0.5 mL of phosphate buffered saline (PBS, n=31); the treatment tested the application of 250 μg of PGE2 (n = 29), making a total of 89 prepubertal mice (BALB/c). Mice were euthanized 14 to 15 h after treatments to detect ovulation and tissue collection. A Chi-square test was used to compare the proportion of animals ovulating. Gene expressions and number of ovulation were analyzed by one-way ANOVA and Tukey’s test was used to compare means among groups. A greater proportion of mice (P < 0.001) ovulated after receiving GnRH (89.7%, 26/29) compared to PGE2 group (58.6%, 17/29). However, the proportion was higher compared to those treated with PBS (0%, 0/31). Ep2 gene expression in the pituitary was > two-fold higher (P < 0.05) in the PGE2 group compared to the PBS and GnRH groups. Further, PGE2 stimulated Cox1 (2.7 fold, P < 0.05) while GnRH stimulated Cox2 expression (6.5 fold, P < 0.05) in the pituitary when compared to the PBS group. In conclusion, our results support the hypothesis that PGE2 can induce ovulation in prepubertal mice with a concomitant increase in Ep2 and Cox1 gene expression in the pituitary gland.

This study aimed to evaluate the role of prostaglandin F2α (PGF) on ovulation. In Experiment 1, cows were randomly allocated to two treatments to receive 150 μg of d-Cloprostenol (PGF Group, n = 12) or 2 mL of NaCl 0.9% (Control Group, n = 11) and CIDRs, were removed 4 days later. No cow ovulated in Control and PGF groups. In Experiment 2, cows were randomly separated into two experimental groups to receive 4 injections of 150 μg of d-Cloprostenol (n = 9) or 2 mL of NaCL 0.9% (n = 9). In this experiment, ovulation was not observed in any cows. In Experiment 3, ovariectomized cows receive three injections of 300μg of PGF analog (PGF Group, n = 5), 100μg of Lecirelin (GnRH Group, n = 5) or 2 mL of PBS (Control Group, n = 4). The LH concentration was higher (P 11.5 mm) were treated with Saline (Control Group, n = 6); Lecirelin (GnRH Group, n = 7) or Cloprostenol Sodium (PGF Group, n = 6). There was a significant increase in the vascular area of follicles from 0 to 24 h in GnRH and PGF treatments. In conclusion, PGF was not able to induce ovulation in cows with high or low plasma progesterone concentration. Additionally, PGF alone was not able to induce LH release and follicle luteinization, but increased follicular vascularization.

This study evaluated the effect of a prostaglandin F2? (PGF) analogue as an ovulatory stimulus in dairy cows and buffaloes raised in the Amazon biome. To this end, three experiments were performed in the state of Rondônia, located in the Amazon biome. In Experiment 1, 22 lactating dairy buffaloes received 2 mg of intramuscular (I.M.) estradiol benzoate (EB) on day 0 and an intravaginal progesterone-releasing device (CIDR) from day 0 to day 9 of the protocol. On days 8 and 9, all cows were given 500 ?g of I.M. d-cloprostenol (PGF analogue). On day 10, buffaloes were divided into two groups to receive 500 ?g of PGF (PGF group, n = 8) or no treatment (CTL group, n = 14), respectively. In Experiment 2, 16 lactating crossbred dairy cows (Holstein x Gir) received 2 mg of EB on day 0 and a CIDR insert from day 0 to day 8. On days 7 and 8, all cows were given 500 ?g of d-cloprostenol. On day 9, cows were divided into two groups to receive 500 ?g of d-cloprostenol (PGF group, n = 8) or no treatment (CTL group, n = 8), respectively. In Experiment 3, 16 lactating crossbred dairy cows (Holstein x Gir) were handled and treated similarly as in Experiment 2, although cows did not receive d-cloprostenol on day 8. Single-point outcome variables were analyzed using one-way analysis of variance (ANOVA), while proportions with dichotomous outcomes were analyzed with the chi-square test. In Experiment 1, there was no difference (P = 0.30) in the ovulation rate between groups, and, on average, 68% of the buffaloes ovulated. Moreover, the treatment did not affect the interval to ovulation (P = 0.61) nor the diameter of the preovulatory follicle (P = 0.47). As for Experiment 2, only one cow, from the PG group, did not ovulate. There were no differences between the CTL and PG groups (P = 0.69) in the moment of ovulation, which occurred in average 82 h after CIDR removal. Finally, in Experiment 3, cows treated with PGF ovulated earlier than those in the CTL group (62.5 ± 5.8 and 94.5 ± 13.5 h, respectively; P = 0.05). Collectively, these results suggest that PGF hastens ovulation in lactating dairy cows, whereas no effect was observed in dairy buffaloes.

The aim of this study was to compare the J-Synch and conventional protocols associated with estrus detection in beef heifers and to compare pregnancy rate between non-lactating cows displaying estrus or not during the J-Synch protocol. In Experiment 1, heifers were subjected to timed artificial insemination (AI) in a conventional protocol with ECP (n=147) or J-Synch protocol plus eCG (n=149). The AI occurred 12 hours after estrus expression; or 48 (Conventional protocol) and 72 hours (J-Synch protocol) after device removal for animals not displaying estrus. The J-Synch group received 10 µg of GnRH at AI. In Experiment 2, the JSynch was performed (n=116 cows), but without eCG injection, and estrus was monitored. Pregnancy rate was not different between protocols in Experiment 1 (Conventional: 50.68%; J-Synch: 60.4%). Heifers that displayed estrus had higher pregnancy rate only in the conventional protocol. In Experiment 2, pregnancy rate was not different between cows that displayed estrus or not. Therefore, performing AI earlier according to estrus expression increases pregnancy rate in conventional protocol, however it does not increase pregnancy rate in the J-Synch protocol.

A ação do hormônio Lactogênio Placentário Bovino (bLP) no metabolismo materno ainda é pouco conhecida. Alguns marcadores, como a proteína de fase aguda Paraoxanase (PON1), são utilizados como indicadores da função hepática auxiliando na determinação da condição metabólica no período de transição em vacas leiteiras. O objetivo deste trabalho foi avaliar a atividade sérica de PON1 durante o periparto em vacas leiteiras com diferentes níveis de bLP. As vacas foram divididas em três grupos de acordo com as concentrações plasmáticas de bLP, em que BAIXO < 2,68 ng mL-1 (n=6), MÉDIO > 2,68 ng mL-1 e < 2,80 ng mL-1 (n=6) e ALTO > 2,80 ng mL-1 (n=6). O período experimental ocorreu entre os 21 dias pré-parto e 28 dias pós-parto. Amostras de soro foram coletadas para a determinação das concentrações de bLP e atividade sérica de PON1. Houve diferença entre os três grupos (P ? 0,0001) de acordo com as concentrações de bLP, assim como entre os dias coletados (P ? 0,0001). No pré-parto, os níveis de PON1 apresentaram diferença entre grupos (P ? 0,05) e coletas (P ? 0,05). Vacas com alta concentração de bLP apresentaram menor atividade sérica de PON1 (P ? 0,05), enquanto vacas com baixos níveis do hormônio obtiveram maior atividade da enzima (P ? 0,05). No pós-parto não houve diferença entre grupos (P ? 0,10), houve diferença entre os dias coletados (P ? 0,0001) e interação entre grupos e coletas (P ? 0,01). O grupo com altas concentrações de bLP apresentou menores níveis de PON1 (P ? 0,01), enquanto vacas do grupo com baixo bLP mantiveram maiores concentrações de PON1 (P ? 0,01). Conclui-se que, vacas com maiores concentrações de bLP no período pré-parto apresentam redução na atividade sérica da enzima PON1 durante o período periparto.

The transition period of dairy cows is characterized by several metabolic alterations, due to the negative energy balance, which negatively affects fertility. The aim of this study was to evaluate the effect of supplementing the in vitro maturation medium with serum from dairy cows at early and late lactation in the oocyte maturation on the rates of nuclear maturation, cleavage and initial embryo development. The cumulus-oocyte complexes (COCs) were randomly divided into treatments: LL: serum from four cows at 354 ± 3.8 days in milk (DIM); and EL: serum from four cows at 10.8 ± 4.8 DIM. Subsequently, the COCs were submitted to maturation, fertilization; and in vitro culture in an incubator at 39°C with 5% CO2. For analysis of nuclear maturation; oocytes were collected after IVM, denuded and stained with Hoechst®. No difference was observed in the number of oocytes that reached metaphase II among treatments. The cleavage rate was not different between LL (59.3%; 320/540) and EL (47.0%; 243/517) treatments (P>0.05), as embryonic development between LL (15.0%; 81/540) and EL (16.6%; 86/517) (P>0.05). It was concluded that supplementation with serum from cows at different lactation periods during the bovine oocyte IVM did not influence the results of in vitro embryo production.

ABSTRACT: Previous studies have evaluated the effects of different reproductive procedures on discomfort markers in sheep and cattle. Such studies may help stimulate the adoption of techniques that are more beneficial for animal welfare. However, markers that are commonly used to evaluate discomfort are highly influenced by external factors. To overcome this, several systemic markers can be evaluated to more precisely identify stress, pain, and inflammation. Such markers include cortisol, acute phase proteins, bradykinin, and substance P. We aimed to review the potential markers of stress, pain, and inflammation, and discuss how and when they are regulated after different stimuli related to reproductive procedures in cattle and sheep. Furthermore, we aimed to review how reproductive procedures with different degrees of invasiveness cause stress and provide information that may help develop strategies to limit animal discomfort.

ABSTRACT: The aim of this study was to estimate neosporosis seroprevalence and its associated risk factors in milk herds (Bos taurus taurus) located in the northwestern region of Rio Grande do Sul State, Brazil. Three hundred twenty-two blood samples were collected from dairy cows on 18 farms in 17 cities of this region. An epidemiologic questionnaire was completed for each farm. It consisted of questions about the general characteristics of the herd, reproduction, and animal management. Serum samples were tested for Neospora caninum using a commercial enzyme-linked immunosorbent assay (ELISA) kit. Results indicated a seroprevalence of Neospora in 88.9% (16/18) of herds and 31.1% (100/322) of individuals. Risk factor analyses demonstrated that culling by reproductive disorder (OR = 0.6), flooding (OR = 0.5), and commercial sale (OR = 0.4) were associated with seroprevalence. Nevertheless, the purchase of replacement animals in the herd played an important role in disease occurrence (OR = 2.2). Results of this study suggested that Neospora caninum was present in the studied herds under investigation and that there are risk factors associated with its seroprevalence on the farms of the northwestern of Rio Grande do Sul.

The liver is an organ with a differential value on the market. However, due to its metabolic functions it is susceptible to various types of alterations, including a large rate of disposal by perihepatitis. The aim of this study was to evaluate the sensitivity and specificity of the diagnosis of perihepatitis by the Federal Inspection Service (FIS), according to histopathological examination and correlate these findings with plasmatic concentrations of AST and GGT. One hundred and fifty four culled sows of the Landrace breed were used. Slaughter was performed by the method of desensitization by electrical stimulation and subsequent exsanguination. Then 5 mL of whole blood was collected to evaluate concentrations of GGT and AST. During evisceration, liver condition was assessed by visual inspection and classified as good or condemned by perihepatitis. Also, fragments of the liver were collected to histopathologic examination. The alterations in the liver parenchyma were classified as degenerative, inflammatory or reparative. The alterations found in liver tissues, considered as perihepatitis by visual inspection, were often due to fibrosis, fatty degeneration or mild hepatitis. The serum concentrations of GGT were high. Moreover, it concentrations were higher in livers with lesions of inflammatory and degenerative nature when compared to livers without injuries (p0.05). Concluding, the perihepatitis diagnosis from the FIS showed low specificity and sensitivity, and the enzyme GGT was a good indicator of liver injuries in swine.

The objective of this study was to evaluate the influence of the ovulatory follicle diameter on the reproductive performance of lactating beef cows subjected to low progesterone fixed-time artificial insemination (FTAI) protocols. Ninety-three lactating beef cows (60-80 days postpartum) at random stages of estrous cycle were given a luteolytic dose of prostaglandin F2α (500 μg cloprostenol; PGF) twice, 11 d apart. Ten days after the second PGF treatment, cows were given 1.5 mg of estradiol benzoate im and a progesterone-releasing intravaginal device (Cue-Mate) with a single pod containing 0.78 g progesterone (Day 0). Cows received another luteolytic dose of PGF on Day 0. On Day 8, the Cue-Mate was removed. Fifty-four to 56 hours later, cows received 12.5 mg of porcine LH (pLH) i.m. and were concurrently artificially inseminated. Ultrasound examinations of the ovaries were performed on Days 10 and 17 to evaluate the diameter of ovulatory follicle and corpus luteum, respectively. Cows which presented ovulatory follicle > 19 mm resulted in larger corpus luteum than cows that had ovulatory follicle

The objective of this study was to evaluate the plasma concentrations of insulin-like growth factor-I (IGF-I), and the mRNA hepatic expression of IGF-I and of the growth hormone receptors GHR and GHR 1A, in postpartum beef cows. Four Angus and four crossbred (Angus x Nelore) postpartum suckled beef cows were used. Liver and blood samples were collected every 10 days, from calving to 40 days postpartum, for gene expression and for β-hydroxybutyrate and IGF-I assays, respectively. Samples for progesterone assay were collected every other day, from day 10 to 40 postpartum. Three cows ovulated before 40 days postpartum. IGF-I concentration was higher in Angus x Nelore than in Angus cows. There was no difference in the expression of GHR, GHR 1A and IGF-I according to breed or ovulatory status. IGF-I concentrations were higher in crossbred cows, but have not changed according to postpartum ovulatory status. Moreover, changes in postpartum IGF-I concentrations are not associated with changes in liver GHR, GHR 1A and IGF-I mRNA expression in either breed.O objetivo deste estudo foi avaliar as concentrações plasmáticas do fator de crescimento semelhante à insulina tipo I (IGF-I) e a expressão hepática de mRNA de IGF-I e dos receptores do hormônio de crescimento GHR e GHR 1A, no pós-parto de vacas de corte. Quatro vacas Angus e quatro mestiças (Angus x Nelore) lactantes foram usadas durante o período de pós-parto. As coletas de tecido hepático e de sangue foram realizadas a cada dez dias, do parto até 40 dias pós-parto, para a avaliação da expressão gênica, e análise de β-hidroxibutirato e IGF-I, respectivamente. As amostras para análise de progesterona foram coletadas a cada dois dias, dos dez aos 40 dias pós-parto. Três vacas ovularam antes dos 40 dias pós-parto. A concentração de IGF-I foi maior em vacas Angus x Nelore do que em vacas Angus. Não houve diferença na expressão hepática de GHR, GHR 1A e IGF-I de acordo com a raça ou com a ovulação. As concentrações de IGF-I foram maiores em vacas cruzadas, e não mudaram com o status ovulatório pós-parto. Além disso, as mudanças observadas na concentração de IGF-I, durante o período pós-parto, não estão associadas a alterações na expressão hepática de mRNA de GHR, GHR 1A e IGF-I, em nenhuma das duas raças.

Foi realizado um estudo para identificar parâmetros de desempenho associados a indicadores de eficiência durante o parto de fêmeas suínas. Foram coletados os seguintes dados de 636 partos e 7.100 leitões nascidos: ordem de parto, número de leitões nascidos vivos, natimortos, mumificados, total de nascidos, aplicação de ocitocina, uso de palpação vaginal, momento do nascimento de cada leitão e do início e final do parto. O intervalo médio de nascimento dos leitões foi de 16,7 minutos e a duração média do parto, de 247 minutos. A duração média do parto aumentou conforme o total de leitões nascidos, o uso de ocitocina e a ocorrência de palpação vaginal. O total de nascimentos nos partos longos (> 211 min), de 13,1 leitões, foi maior que nos partos curtos (< 210 min), de 11,7 leitões, portanto, quanto maior o total de nascidos, maior a duração do parto. As leitegadas foram maiores nas fêmeas de segundo parto (12,8) em comparação àquelas de primeiro parto (11,9). A duração do parto é influenciada pelo total de leitões nascidos, que é maior em fêmeas de segundo parto e está associada à maior ocorrência de leitões natimortos e mumificados.This study aimed to identify some performance parameters associated with the farrowing efficiency in sows. From a total of 636 births and 7,100 piglets born, data was collected for: parity (OP), number of piglets born alive (NV), stillborns (NAT), mummified (MUM), total litter size (TN), use of vaginal palpation and oxytocin injection, time of birth for each piglet, and beginning and end of the parturition. The average interval among piglets birth was 16.7 min and the average duration of parturition was 247 min. The average duration of parturition increased regarded to the number of born piglets, the use of oxytocin and with the ocurence of vaginal palpation. The total number of births in the long parturitions (> 211 min), with 13.1 piglets was higher than in the short parturitions (< 210 min), with 11.7 piglets, therefore, the higher the number of total piglets born, the longer is the duration of parturition. Litter size was higher for sows of the second parity (12.8) than for sows of first parity (11.9). The duration of parturition is affected by the number of piglets born, which is higher in second parity than first parity females and it is associated to the higher occurence of stillbirths and mummified piglets.

This study aim to evaluate the quality of boar semen stored at different temperatures and media on PIGPEL5 extender, using egg yolk as an external membrane protector, and on PIGPEL5Plus, containing low density lipoprotein (LDL) as protector. In the experiment 1, the semen doses were stored in a semen container at 5 and 17 °C and the results were compared with semen stored at 17 °C in BTS extender. In the experiment 2, the doses with the PIGPEL5 and PIGPEL5Plus extenders were stored in a commercial refrigerator and in semen container, both at 5 °C. The use of extenders with extracellular cryoprotectant (PIGPEL5 e PIGPEL5Plus) showed higher (p < 0.05) motility values in comparison to BTS until 48 h. Furthermore, the use of extracellular cryoprotectant was good to maintenance of membrane integrity and normal morphology at 5 oC similarly to 17 oC extenders. There was no difference (p > 0.05) in the motility, membrane integrity and morphology for the substitution of egg yolk (PIGPEL5) for LDL (PIGPEL5Plus). In experiment 2, also there was no difference (p > 0.05) in motility, membrane integrity and morphology between extenders and type of container until 72 h. The conservation of semen on PIGPEL5 extender and commercial refrigerator (5 ºC) allowed patterns of sperm quality according recommended for AI.Este estudo avaliou a qualidade do sêmen suíno preservado em diferentes temperaturas e meios de conservação no diluente PIGPEL5, utilizando gema de ovo como protetor externo de membrana, e no diluente PIGPEL5Plus, utilizando lipoproteína de baixa densidade (LDL) como protetor. No experimento 1, as doses de sêmen foram conservadas em refrigerador de sêmen a 5 e 17 °C nos diluentes PIGPEL5 e PIGPEL5Plus e comparadas ao diluente BTS a 17 °C. Já no experimento 2, foi comparada a conservação do sêmen nos diluentes PIGPEL5 e PIGPEL5Plus em geladeira convencional ou em refrigerador de sêmen a 5 ºC. Observou-se que o uso de diluidores com crioprotetor extracelular (PIGPEL5 e PIGPEL5Plus) apresentou maiores (p < 0,05) resultados de motilidade com relação ao BTS até 48 h. Além do mais, o uso de crioprotetor extracelular foi benéfico para a manutenção da integridade e morfologia normais a temperatura de 5 ºC em níveis similares aos diluidores a 17 ºC. Não houve diferença (p > 0,05) na motilidade, integridade de membrana e morfologia para a substituição da gema de ovo (PIGPEL5) pela LDL (PIGPEL5Plus). No experimento 2, também não houve diferença na motilidade, integridade de membrana e morfologia espermática entre os diluentes e formas de acondicionamento testados até 72 h (p > 0,05). O acondicionamento do sêmen no diluente PIGPEL5 em geladeira doméstica (5 ºC) proporcionou padrões de qualidade espermática de acordo com o recomendado para a IA.

Os objetivos neste experimento foram avaliar o efeito do tempo de exposição a um progestágeno (P4) na taxa de prenhez de novilhas púberes e pré-púberes inseminadas em tempo-fixo (IATF) e estudar o retorno econômico dos protocolos utilizados, por meio da comparação desses protocolos ao sistema tradicional de acasalamento natural aos 26 meses de idade. Foram utilizadas 114 novilhas da raça Bradford com 16 meses de idade, classificadas em quatro grupos de acordo com o tratamento e a maturidade sexual: GPPLP - pré-puberes, longo tratamento com P4 (n=21); e GPPCP - pré-puberes, curto tratamento com (n=19); GPLP - púberes, longo tratamento com P4 (n=34); e GPCP - púberes, curto tratamento com P4 (n=40). As novilhas do GPPLP e GPLP receberam no dia -8 um pessário intravaginal impregnado com acetato de medroxiprogesterona. No dia 0, o pessário foi removido e outro foi inserido, juntamente com uma injeção de 2,5 mg de benzoato de estradiol (BE). No dia 8, o pessário foi retirado e as novilhas receberam 0,5 mg de BE e 250 µg de cloprostenol sódico. A inseminação artificial em tempo fixo (IATF) foi realizada 54 horas depois. As novilhas do GPPCP e GPCP receberam o mesmo tratamento de sincronização dos grupos GPPLP e GPLP, com exceção do AMP do dia -8 ao dia 0. A taxa de prenhez foi maior nas novilhas púberes (60,3%) que nas pré-puberes (35,0%). No entanto, não foi detectado efeito do tempo de tratamento na taxa de prenhez nas novilhas púberes e pré-puberes. A resposta econômica na utilização de protocolos com P4 foi maior em novilhas aos 16 meses que no sistema de acasalamento aos 26 meses. A exposição prolongada a um P4 não foi eficiente para aumentar a taxa de prenhez de novilhas submetidas a IATF.The aim of this experiment was to evaluate the effect of the duration of progestagen (P4) exposure and sexual maturity of prepubertal and pubertal heifers submitted to timed artificial insemination (TAI). A hundred and fourteen 16- month old Bradford heifers were classified, according treatment and sexual maturity, in 4 groups: PPLPG (prepubertal long exposure to P4, n=21), PPSPG (prepubertal short exposure to P4, n=19), PLPG (pubertal long exposure to P4, n=34) and PSPG (pubertal short exposure to P4, n=40). On day -8, the heifers from PPLPG (prepubertal long exposure to progestagen) and PLPG (pubertal long exposure to progestagen) received an intravaginal sponge impregnated with medroxiprogesterone acetate (MAP). On day 0 the sponge was removed and a new sponge was inserted, together with an injection of 2.5 mg estradiol benzoate (EB). On day 8 the sponge was removed and the heifers received an injection of 0.5 mg EB and 250 ìg sodium cloprostenol. The TAI was performed 54 hours after sponge withdrawal. The heifers from PPSPG and PSPG received the same synchronization treatment, except for the additional MAP from day -8 to day 0. The pregnancy rate was higher in pubertal (60.3%) than in pre-pubertal (35.0%) heifers. However, there was no effect of the duration of treatment in the pregnancy rate between pubertal and prepubertal heifers. The second part of this study aimed to evaluate the economical return of the protocols and compare them with the traditional breeding system at 26 months of age. A better economic response with the use of protocols associating P4 in heifers at 16 months was observed compared to the traditional system at 26 months of age. The prolonged exposure to P4 did not improved pregnancy rate in heifers submitted to TAI.

Objetivou-se verificar a redução de perdas embrionárias por meio do bloqueio da secreção de prostaglandina com a utilização de flunixin meglumine (FM) e avaliar o retorno econômico desta técnica. No experimento 1, utilizaram-se vacas de corte no pós-parto e, no experimento 2, somente novilhas. Todas as fêmeas foram sincronizadas e inseminadas em tempo fixo (IATF) e, após 14 dias da IATF, foram distribuídas em dois grupos: grupo flunixin meglumine (GFM), composto de 59 vacas no experimento 1 e 23 novilhas no experimento 2; e grupo controle (GC), de 56 vacas no experimento 2 e 20 novilhas no experimento 1, que receberam ou não flunixin no dia 14, respectivamente. O tratamento com flunixin não influenciou a taxa de prenhez, que, no experimento 1, foi de 42,4% no grupo flunixin e 42,8% no grupo controle e, no experimento 2, de 39,1% no grupo flunixin e 25,0% no grupo controle. Verificou-se rentabilidade de 21,62; 9,24; 14,36 e 12,06% para os protocolos dos grupos controle e flunixin dos experimentos 1 e 2, respectivamente. A taxa de prenhez não foi influenciada pelo uso de flunixin meglumine no dia 14 após inseminação artificial em vacas no pós-parto e novilhas inseminadas em tempo fixo.This study aimed to evaluate the effectiveness and the economical advantage of using flunixin meglumine (FM) to block uterine secretion of prostaglandin in order to reduce embryonic losses in beef cattle females. Postpartum cows (E1) and heifers (E2) were submitted to estrus synchronization and inseminated at fixed time. Fourteen days after the insemination the animals were assigned to the FM treatment group (FMG, including 59 cows and 23 heifers) and to the control group (CG, including 56 cows and 20 heifers). Pregnancy rates (42.4% for FMG and 42.8% for CG in E1) and (39.1% for FMG and 25.0% for CG in E2) did not differ between groups. Estimates of net income were 21.62, 9.24, 14.36 and 12.06% for the CG e FMG protocols in cows and in heifers, respectively. The use of FM at 14 days after AI did not affect pregnancy rates of postpartum beef cows and heifers.

The aim of this study was to evaluate the use of a prostaglandin F2α analogue (PGF2α) and oestradiol benzo-ate (ODB) in estrus synchronization programs. A hundred and eighty five non-lactating females divided in 4 groups were used. G1 (44) and G2 (46) received two applications of PGF2α (D0 and D11) and G3 (26) and G4 (37) received one application after 5 days of estrous detection. G1 and G3 also received a 1 mg ODB application 48 hours after the PGF2α. The pregnancy rate at AI was 42,2% for G1, 47,8% for G2, 32,1% for G3 e 57,6% for G4 (p>0,05) and of 38,4% and 51,4% for animals submitted to FTAI and estrous detection, respectively (p>0,05). This results show that pregnancy rates of females fixed time inseminated didn’t differ of that inseminated after estrus detection. Key-words: Beef cattle, estrus synchronization, fixed time artificial insemination, prostaglandin. O objetivo deste estudo foi avaliar o emprego de um análogo da prostaglandina F2α (PGF2α) em associação ao benzoato de estradiol (BE) em programas de sincronização de cios. Utilizaram-se 185 fêmeas não-lactantes divididas em quatro grupos. O G1 (44) e o G2 (46) receberam duas aplicações de PGF2α (D0 e D11) e os animais do G3 (26) e G4 (37) uma aplicação de PGF2α, após cinco dias de detecção de cio. O G1 e o G3 receberam 1mg de BE 48 horas após a PGF2α. A taxa de prenhez na IA foi de 42,2% no G1, 47,8% no G2, 32,1% no G3 e 57,6% no G4 (p>0,05) e de 38,4% e 51,4% para animais submetidos à IATF e à detecção de cio, respectivamente (p>0,05). Notou-se que a taxa de prenhez nas fêmeas inseminadas em tempo-fixo não diferiu daquelas que foram inseminadas após a detecção de cio. Palavras-chaves: Bovinos de corte, inseminação artificial em tempo fixo, prostaglandina, sincronização de cios.

O objetivo deste experimento foi avaliar o efeito das técnicas transcervical e laparoscópica sobre a taxa de prenhez de ovelhas inseminadas em tempo-fixo. A taxa de prenhez para as técnicas transcervical e laparoscópica foi de 40% (p>0.05). Quanto ao local de deposição do sêmen na inseminação artificial (IA) transcervical, não houve diferença na taxa de prenhez (p>0.05), com taxas de 25.0% na cervical superficial, 43.7% cervical médio, 41.7% cervical profundo e 50.0% intra-uterino. Estes resultados demonstram que a IA transcervical apresenta resultados semelhantes aos obtidos com o uso de laparoscopia, quando estas técnicas são realizadas em tempo-fixo. PALAVRAS-CHAVE: Cérvix, intrauterino, sêmen congelado, tracionamento The objective of this experiment was to evaluate the effect of the transcervical and laparoscopic techniques on the pregnancy rate of inseminated sheep in fixed-time. The pregnancy rate for the transcervical and for laparoscopic techniques was 40% (p>0.05). About the place of deposition of the semen in transcervical artificial insemination (AI), there was not difference in the pregnancy rate (p>0.05), with rates of 25.0% in the superficial cervical, 43.7% in medium cervical, 41.7% in deep cervical and 50.0% intrauterine. These results demonstrate that transcervical AI showed similar results to the obtained with laparoscopy, when these techniques are accomplished in fixed-time. KEY WORDS: Cervix, intrauterine, frozen semen, traction

The aim of this work was to validate a protocol for induction of subacute ruminal acidosis (SARA) (Experiment 1) and test the efficiency of probiotic Saccharomyces cerevisiae or monensin to avoid pH ruminal drops in sheep (Experiment 2). In Experiment 1, six ewes were fasted for two days and then fed most with concentrate during four days. Ewes in this protocol had ruminal fluid pH below 6.0 and kept it for 75 consecutive hours. In Experiment 2, 18 sheep were distributed into three groups: Control (CG, n = 6), monensin (MG, n = 6) and probiotic group (PG, n = 6). SARA was induced according Experiment 1. PG had lower pH (5.7 ± 0.1) than CG (6.0 ± 0.1) (P = 0.05), while MG (5.7 ± 0.1) was similar to both during SARA induction. SARA induction reduced ruminal protozoa population (P < 0.05) and increased chloride concentrations in ruminal fluid (P < 0.01). In serum, SARA increased concentrations of phosphorus (P < 0.01), AST (P < 0.01) and GGT (P < 0.01), but reduced LDH (P < 0.01). In conclusion, the protocol used for SARA induction was able to maintain ruminal pH between 5.5-6.0 for more than 48 hours. However, monensin and probiotics supplementation was not effective in preventing changes in ruminal and serum parameters during SARA.

The effect of pST on the testicular characteristics and metabolic parameters of prepubertal pigs was evaluated. Experiment 1 aimed to determine the interval between applications of pST based on the concentrations of circulating IGF-I. Experiment 2 aimed to evaluate the effect of pST on metabolic parameters, testicular characteristics, and expression of GHR, IGF-I and PCNA. In Experiment 1 twelve piglets with 30 days of age were used. The pST Group (n=6) was submitted to one i.m. injection of pST and the Control Group (n=6) to one placebo injection. Blood collections were performed until d 7 post pST application to determine IGF-I concentration and metabolic profile. In Experiment 2 twelve piglets with 22 days of age were used. The pST Group was submitted to pST injections every three days, and the Control Group received placebo doses during 30 days. Blood collections were performed every 3 days. Samples of liver and testicular tissue were collected to determine gene expression and testicular characteristics. In Experiment 1 IGF-I concentration was higher for the pST Group (P=0.02). In Experiment 2 the pST Group had higher body and testicular weight (P=0.06) and increased gene expression of PCNA in testes (P

The objective of this work was to evaluate the effect of insulin alone or in association with equine chorionic gonadotropin (eCG) on the fertility of postpartum beef cows subjected to synchronization. A total of 340 cows was subjected to fixed time artificial insemination. In the trial 1, the cows were subjected to temporary weaning (TW), while in the trial 2 the same protocol was tested without TW. The addition of an insulin injection to a progesterone/eCG-based protocol without TW increased the pregnancy rate of beef cows with body condition score (BCS) equal to or lower than 2.5. Insulin had no effect on cows submitted to TW or with BCS equal to or higher than 3.0.O objetivo deste trabalho foi avaliar apenas o efeito da insulina ou dela em associação com gonadotrofina coriônica equina (eCG) na fertilidade de vacas em pós-parto submetidas à sincronização. Um total de 340 vacas foi submetido à inseminação artificial em tempo fixo. No experimento 1, as vacas foram submetidas ao desmame temporário (DT), enquanto no experimento 2, o mesmo protocolo foi testado sem DT. A adição de uma injeção de insulina a um protocolo baseado em progesterona/eCG sem DT aumentou a taxa de prenhez de vacas de corte com escore de condição corporal (ECC) igual ou menor que 2,5. A insulina não teve efeito em vacas submetidas a DT ou com ECC igual ou maior que 3,0.

O objetivo deste estudo foi determinar o efeito do adsorvente (ADS) glucomanano modificado sobre parâmetros clínicos, hematológicos e ruminais de ovinos submetidos a dietas contendo aflatoxina (AFLA). Foram utilizadas 22 ovelhas mestiças (Corriedale e Texel), com 18 meses de idade. Os animais foram divididos em quatro grupos, de acordo com a adição de AFLA (1,5 PPM) ou ADS (2 PPM) na fração concentrada da dieta: animais recebendo AFLA na dieta (AFLA; n=6); animais recebendo AFLA e ADS na dieta (AFLA/ADS; n=6); animais recebendo ADS na dieta (ADS; n=5) e grupo controle, sem adição de ADS ou AFLA na dieta (CONTROLE; n=5). As dietas foram fornecidas por um período de 42 dias. Foram realizadas coletas de fluido ruminal a cada sete dias e avaliações clínicas (exame físico geral, urinálise e hemograma) a cada 10 dias. Quanto ao perfil leucocitário, a suplementação com adsorvente aumentou a concentração plasmática de eosinófilos. Os demais parâmetros clínicos e ruminais não foram influenciados pela presença do adsorvente ou da aflatoxina na dieta. Assim, o adsorvente glucomanano modificado influenciou a resposta leucocitária de ovinos, porém sem efeito na função ruminal e nos parâmetros clínicos avaliados.

O objetivo deste estudo foi avaliar o emprego de um análogo da prostaglandina F2α (PGF2α) em associação ao benzoato de estradiol (BE) em programas de sincronização de cios. Utilizaram-se 185 fêmeas não-lactantes divididas em quatro grupos. O G1 (44) e o G2 (46) receberam duas aplicações de PGF2α (D0 e D11) e os animais do G3 (26) e G4 (37) uma aplicação de PGF2α, após cinco dias de detecção de cio. O G1 e o G3 receberam 1mg de BE 48 horas após a PGF2α. A taxa de prenhez na IA foi de 42,2% no G1, 47,8% no G2, 32,1% no G3 e 57,6% no G4 (p>0,05) e de 38,4% e 51,4% para animais submetidos à IATF e à detecção de cio, respectivamente (p>0,05). Notou-se que a taxa de prenhez nas fêmeas inseminadas em tempo-fixo não diferiu daquelas que foram inseminadas após a detecção de cio. Palavras-chaves: Bovinos de corte, inseminação artificial em tempo fixo, prostaglandina, sincronização de cios.

O objetivo deste experimento foi avaliar o efeito das técnicas transcervical e laparoscópica sobre a taxa de prenhez de ovelhas inseminadas em tempo-fixo. A taxa de prenhez para as técnicas transcervical e laparoscópica foi de 40% (p>0.05). Quanto ao local de deposição do sêmen na inseminação artificial (IA) transcervical, não houve diferença na taxa de prenhez (p>0.05), com taxas de 25.0% na cervical superficial, 43.7% cervical médio, 41.7% cervical profundo e 50.0% intra-uterino. Estes resultados demonstram que a IA transcervical apresenta resultados semelhantes aos obtidos com o uso de laparoscopia, quando estas técnicas são realizadas em tempo-fixo. PALAVRAS-CHAVE: Cérvix, intrauterino, sêmen congelado, tracionamento

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