RESUMO Avaliou-se o tratamento com hCG na resposta ovariana e na taxa de prenhez utilizando protocolo de sincronização do estro de nove dias em ovelhas Santa Inês. As ovelhas receberam um dispositivo intravaginal de progesterona em fase aleatória do ciclo (dia zero= D0). No momento da remoção do dispositivo (D9), as fêmeas receberam 30µg de d-cloprostenol (Prolise®, Syntex, Argentina) e 250UI de eCG (Folligon®, Intervet, Brasil). Nesse momento, as ovelhas foram aleatoriamente distribuídas em dois grupos de tratamento: controle sem indução de ovulação e tratamento com 500UI hCG para indução de ovulação. As ovelhas dos grupos controle e hCG foram inseminadas 60h e 48h após a remoção do dispositivo, respectivamente. Não houve diferença entre os grupos para o diâmetro do primeiro e do segundo folículo pré-ovulatório. As avelhas do grupo hCG apresentaram menor intervalo entre a remoção do dispositivo e a ovulação (grupo controle: 79.9±15.4h e grupo hCG: 54.7±4.9h; P=0.001) e maior sincronização das ovulações. No entanto, o tratamento com hCG diminuiu a taxa de prenhez após a IATF (P=0,009). Conclui-se que, apesar de a administração de hCG aumentar a sincronização da ovulação, reduz a taxa de prenhez.

ABSTRACT The aim of this study was to evaluate hCG treatment on ovarian response and on pregnancy rate using a 9-day oestrus synchronization protocol in Santa Ines ewes. On a random oestrus cycle day, ewes received an intravaginal progesterone device (Primer-PR®, Tecnopec, Brazil). Nine days later (Day 9), 30µg of d-cloprostenol (Prolise®, Syntex, Argentina) and 250IU of eCG (Folligon®, Intervet, Brazil) were administered and the progesterone device was removed. This moment, the ewes were randomly assigned on two groups: Control Group and hCG Group. In the hCG Group, the ewes received 500IU of hCG (Vetecor®, Hertape-Calier, Spain) 24h after device removal. In the Control Group, the ewes did not receive any ovulation inductor. Control and hCG Groups ewes were inseminated 60h and 48h after device removal, respectively. There was no difference between the groups regarding the first ovulatory follicle diameter and the second ovulatory follicle. hCG Group ewes had shorter interval between device removal and ovulation (Control: 79.9±15.4h and hCG: 54.7±4.9h; P=0.001) and more synchronized ovulations. However, the treatment with hCG decreased the pregnancy rate after TAI (P=0,009). In conclusion, hCG administration improves ovulatory synchronisation, but causes a decrease in the pregnancy rate.

A metadona é um opioide pouco utilizado na medicina veterinária, e há, ainda, questionamentos quanto ao seu uso. Desse modo, comparou-se o emprego da metadona, administrada pelas vias IM e IV, e avaliaram-se seus efeitos sobre as características cardiorrespiratórias e os tempos de extubação e recuperação em cadelas submetidas à ovariossalpingo-histerectomia. Utilizaram-se 16 cadelas, pré-medicadas com levomepromazina, 0.6mg/kg, IM. Após 20 minutos, a indução anestésica foi feita com propofol, 5mg/kg, IV, e a manutenção com isoflurano. Transcorridos 10 minutos, os animais receberam metadona, 0.3mg/kg, pelas vias IM - grupo GIM - e IV - grupo GIV. As mensurações das frequências cardíaca (FC) e respiratória (FR), pressão arterial média (PAM), temperatura esofágica (TE), pressão parcial de dióxido de carbono (EtCO2) e saturação de oxi-hemoglobina (SpO2) foram registradas antes da administração do opioide (T0), após 20 minutos (T1) e a cada 10 minutos da administração até 60 minutos (T2 a T5). Usou-se a análise de perfil (5%). Com relação à FC, PAM, FR, EtCO2, TE e SpO2, não foram observadas diferenças significativas entre grupos e momentos. Observaram-se tempos de extubação e recuperação maiores no GIV. É possível concluir que a administração IV e a IM da metadona não produzem alterações nas características cardiorrespiratórias em cadelas.

Methadone is a little used opioid in veterinary practice, and there are still questions about its use. The objective of this study was to evaluate the effects of intramuscular (IM) or intravenous (IV) administration of methadone on cardiopulmonary parameters and times of extubation and recovery in female dogs submitted to ovariohysterectomy. Sixteen adult female dogs were used and premedicated with levomepromazine (0.6mg/kg, IM). After 20 minutes, propofol (5mg/kg, IV) was used for induction and anesthesia was maintained with isoflurane. After 10 minutes, methadone at 0.3mg/kg was administered intravenously in IVG and intramuscularly in IMG. The measurement of heart (HR) and respiratory rates (RR), median arterial pressure (MAP), esophagic temperature (ET) and concentration of end-tidal carbon dioxide (PE'CO2) was performed immediately before the administration of the opioid (T0), after 20 minutes (T1) and then at 10-minute intervals (T2, T3, T4 and T5). The statistical analysis used was profile (5%). HR, APM, RR, PE'CO2, BT and SpO2 did not differ significantly among times or between groups at any time. Times of extubation and recovery were higher in IVG. It is possible to conclude that IV and IM administration of methadone did not produce changes in the cardiorespiratory parameters of that specie.

The research was done between december 2001 and may 2002 in Macaé-RJ. This producers belonged to the Macaé Cooperated Producers, having 1646 cows. The work aimed to collect data for two reports, one operational and other of performance, where producers could take administrative decisions. During the research 168 monthly reports were done. Using the operational report, the producers monitored the reproductive and productive status of each cow and the performance report allowed to have the productive and finance indexes under control by the individual monthly production cost. By using the monthly real production cost, it was expected that producers could take decisions to improve the management of their properties, using technologies to reduce their real production costs. The results showed that was possible to reduce in 0.3% the cost per litre of milk, in 2.5% the total production cost. The monthly production not increased -0.6% and cow productivity increased 3.6%.

O objetivo foi a coleta de dados no período de dezembro de 2001 a maio de 2002, no município de Macaé-RJ, com a participação inicial de 15 produtores cooperados da Cooperativa Agropecuária de Macaé, RJ, participando com plantel total de 1646 vacas, a fim de gerar relatórios como operacional e de performances, onde os produtores podiam tomar decisões de cunho administrativo. Foram emitidos 168 relatórios, com periodicidade mensal. Com o relatório operacional os produtores monitoravam a situação reprodutiva e produtiva de suas matrizes, e com o relatório de performances os seus índices zootécnicos e suas despesas, com ênfase no custo de produção mensal da leite. Através do custo de produção mensal, esperou-se que os produtores tomassem decisões voltadas à gestão de suas propriedades, dessa forma exigindo tecnologias que fossem capazes de reduzir seus custos. Os resultados mostraram que os produtores conseguiram nesse período, reduzir o custo médio do litro de leite em 0,3%, redução média na despesa mensal da ordem de 2,5%, redução na produção média mensal da ordem de -0,6% e, incremento na produtividade por vaca/dia da ordem de 3,6%.

Fragmentos da junção uterovaginal de 16 exemplares de fêmeas adultas de peru foram examinados, com o objetivo de determinar as modificações morfométricas e histológicas dos túbulos armazenadores de espermatozoides (SST), durante os períodos de atividade e repouso reprodutivo. Os estudos foram realizados a partir de dissecações do oviduto esquerdo, utilizando-se técnicas histológicas, histoquímica e histométricas de rotina. Essas estruturas originam-se de invaginações do epitélio das pregas da região uterovaginal e apresentam-se tubulosas, simples e não ramificadas, com epitélio formado por células prismáticas estreitas, claras e escuras, com núcleo vesiculoso basal e microvilos apicais. As secreções dessas células apresentaram reações negativas para PAS e Alcian Blue, indicando ausência de mucossubstâncias. Os parâmetros morfométricos utilizados mostraram que há diferenças significativas entre os períodos de atividade reprodutiva e de repouso. Na fase de atividade reprodutiva, o comprimento tubular, o volume tubular, o volume do lume, o número de SST na junção uterovaginal, o diâmetro externo e interno, a altura celular e o número de células por túbulos estão aumentados, e observam-se espermatozoides agrupados na luz do lume e células claras e escuras nos túbulos com vesículas supranucleares no citoplasma das células tubulares. Na fase de repouso, os parâmetros morfológicos estão reduzidos e não são encontrados espermatozoides na luz do lume. Nesta fase, não são evidenciadas as células escuras nem as vesículas supranucleares no citoplasma celular.

Fragments of the uterus-vaginal junction of 16 adult female turkeys were investigated aiming to determine the morphometrical and histological modifications in the tubuli spermatici (tubular sperm glands) during the breeding (August to March) and non-breeding (April to July) seasons. The studies were performed in dissected oviducts processed for histology, histochemistry, and morphometry of the tubuli spermatici (TS), structures which are originated from invaginations of the uterus-vaginal epithelium. TS are simple tubular glands, lined by a columnar epithelium formed by light and dark narrow cells, which presented euchromatic nucleus and apical microvillus. The TS epithelium secretion was negative for PAS and Alcian Blue stains, indicating the absence of mucosubstances. The tubular length, tubular volume, luminal volume, number of TS, as well as external and internal diameter, cellular height, and number of cells per tubule showed significant differences between the reproductive phases (breeding and non-breeding). In the breeding season, all these morphometrical parameters were increased when compared with the ones from the non-breeding season. Clusters of sperm in the lumen of the glands, as well vesicles in the cytoplasm of both light and dark epithelial cells, were observed in the breeding season. In the non-breeding season, luminal sperm, vesicles, and dark cells were not observed in the TS glands.

Serum hormone levels were compared between captive and free-living maned wolves and seasonal variations of sex hormones were studied. Blood samples were collected from 16 male and 26 female adult animals from Brazilian zoos, and from 30 male and 24 female free-living adults to determine serum progesterone and testosterone by radioimmunoassay. Serum testosterone concentrations varied (P < 0.05) across seasons for 16 captive males, being higher in autumn (2184.7 ± 355.1 pg/mL) than in summer (1080.7 ± 205.4 pg/mL), winter (1270.1 ± 276.6 pg/mL) and spring (963.9 ± 248.1 pg/mL), although they did not differ between summer, winter and spring. Testosterone concentration of 30 free-living males differed (P < 0.05) between autumn (824.1 ± 512.2 pg/mL), winter (14.4 ± 8.0 pg/mL) and spring (151.9 ± 90.5 pg/mL). Comparison between captive and free-living animals showed no difference in autumn (P > 0.05). Sixteen captive males showed higher testosterone concentration during winter and spring compared with 30 free-living animals (P < 0.05). Progesterone concentration varied among seasons in 26 captive females (P < 0.05), being higher in autumn (15.3 ± 3.1 ng/mL) than in summer (6.6 ± 1.5 ng/mL), winter (5.3 ± 3.1 ng/mL) and spring (4.3 ± 0.7 ng/mL). Progesterone concentration of 24 free-living females varied between autumn (17.1 ± 6.0 ng/mL) and winter (1.7 ± 0.3 ng/mL) (P < 0.05), but we could not obtain data for spring or summer. No difference in progesterone levels was observed between captive and free-living females in autumn and winter.

Alternative methods to the utilization of laboratory animal blood and its by-products are particularly attractive, especially regarding hamsters due to their small size and difficulties in obtaining serial blood samples. Steroid hormone metabolite quantification in feces, widely used in studies of free-ranging or intractable animals, is a non-invasive, non-stressor, economical, and animal saving technique which allows longitudinal studies by permitting frequent sampling of the same individual. The present study was undertaken to determine the suitability of this method for laboratory animals. Estradiol and progesterone metabolites were quantified by radioimmunoassay in feces of intact, sexually mature female Syrian hamsters during the estrous cycle (control) and in feces of superovulated females. Metabolites were extracted by fecal dilution in ethanol and quantified by solid phase radioimmunoassay. Median estrogen and progesterone concentrations were 9.703 and 180.74 ng/g feces in the control group, respectively. Peaks of estrogen (22.44 ± 4.54 ng/g feces) and progesterone (655.95 ± 129.93 ng/g feces) mean fecal concentrations respectively occurred 12 h before and immediately after ovulation, which is easily detected in this species by observation of a characteristic vaginal postovulatory discharge. Median estrogen and progesterone concentrations (28.159 and 586.57 ng/g feces, respectively) were significantly higher in superovulated animal feces (P < 0.0001). The present study demonstrated that it is possible to monitor ovarian activity in Syrian hamsters non-invasively by measuring fecal estradiol and progesterone metabolites. This technique appears to be a quite encouraging method for the development of new endocrinologic studies on laboratory animals.

Dengue hemorrhagic fever (DHF) is a severe febrile disease, characterized by abnormalities in hemostasis and increased vascular permeability, which in some cases results in hypovolemic shock syndrome and in dengue shock syndrome. The clinical features of DHF include plasma leakage, bleeding tendency and liver involvement. We studied the histopathological features of a fatal case of dengue-3 virus infection. The patient, a 63-year old male, presented with an acute onset of severe headache, myalgia and maculopapular rash. Tissue fragments (liver, spleen, lung, heart, kidney and lymph nodes) were collected for light microscopy studies and stained by standard methods. Histopathology revealed severe tissue damage, caused by intense hemorrhage, interstitial edema and inflammation. Some tissue sections were also processed with the immunoperoxidase reaction, which revealed the dengue viral antigen. Dengue-3 virus was isolated and identified with electron microscopy in a C6/36 cell culture inoculated with the patient's serum. Viral particles were detected in the infected cell culture.

Complex interactions between androgen and estrogen (E2) regulate prostatic development and physiology. We analyzed the early effects of a high single dose of E2 (25 mg/kg body weight) and castration (separately or combined) on the adult 90-day-old male Wistar rat ventral prostate. Androgen levels, prostate weight, and the variation in the relative and absolute volume of tissue compartments and apoptotic indices were determined for 7 days. Castration and exogenous E2 markedly reduced ventral prostate weight (about 50% of the control), with a significant reduction in the epithelial compartment and increased stroma. The final volume of the epithelium was identical at day 7 for all treatments (58.5% of the control). However, E2 had an immediate effect, causing a reduction in epithelial volume as early as day 1. An increase in smooth muscle cell volume resulted from the concentration of these cells around the regressing epithelium. The treatments resulted in differential kinetics in epithelial cell apoptosis. Castration led to a peak in apoptosis at day 3, with 5% of the epithelial cells presenting signs of apoptosis, whereas E2 caused an immediate increase (observed on day 1) and a sustained (up to day 7) effect. E2 administration to castrated rats significantly increased the level of apoptosis by day 3, reaching 9% of the epithelial cells. The divergent kinetics between treatments resulted in the same levels of epithelial regression after 7 days (~30% of control). These results show that E2 has an immediate and possibly direct effect on the prostate, and anticipates epithelial cell death before reducing testosterone to levels as low as those of castrated rats. In addition, E2 and androgen deprivation apparently cause epithelial cell death by distinct and independent pathways.

In order to develop a high-efficiency and reproducible transformation protocol for Stylosanthes guianensis we assessed the biological and physical parameters affecting plant electroporation protoplasts. Energy input, as combinations of electric field strengths discharged by different capacitors, electroporation buffer and DNA form were evaluated. Transformation efficiency was assayed in vivo as transient reporter gene expression, using the GFP-coding gene mgfp5 driven by a CaMV 35S constitutive promoter. Energy input and electric field strength had a critical influence on transgene expression with higher transformation levels being achieved with 250 V.cm-1 discharged by 900 and 1000 muF capacitors. Linear plasmid DNA, the absence of chloride and the presence of calcium ions also increased transient gene expression, albeit not significantly.

The objective of this work was to compare the values of milk somatic cell counts (SCC) using the Somacount 300, and two detergents for sample preparation. The equipment was calibrated using the detergent RBS 35. Forty independent milk samples were analyzed. Each sample was randomly divided into two subsamples, and each subsample was analyzed after preparation with either RBS 35 or Extram MA 01 Alkaline detergents. The correlation coefficient between the two methods was high (0.998). This finding suggests the possibility of substitution of RBS 35 for an economical alternative.

We evaluated the accuracy of a 2nd generation ELISA to detect Helicobacter pylori infection in adults from a developing country in view of variations in sensitivity and specificity reported for different populations. We studied 97 non-consecutive patients who underwent endoscopy for evaluation of dispeptic symptoms. The presence of H. pylori was determined in antral biopsy specimens by culture, by the preformed urease test and in carbolfuchsin-stained smears. Patients were considered to be H. pylori positive if at least two of the three tests presented a positive result or if the culture was positive, and negative if the three tests were negative. Sixty-five adults (31 with peptic ulcer) were H. pylori positive and 32 adults were H. pylori negative. Antibodies were detected by Cobas Core anti-H. pylori EIA in 62 of 65 H. pylori-positive adults and in none of the negative adults. The sensitivity, specificity and positive and negative predictive values of the test were 95.4, 100, 100 and 91.4%, respectively. The Cobas Core anti-H. pylori EIA presented high sensitivity and specificity when employed for a population in Brazil, permitting the use of the test both to confirm the clinical diagnosis and to perform epidemiologic surveys.