RESUMO

Touros em treinamento (n=17) para rodeio foram avaliados quanto a interferência do estresse na produção de testosterona. Foi realizada análise de parâmetros quanto a higidez dos touros antes do treinamento e coleta de sangue. Após o treinamento, foi realizada a segunda coleta de sangue. As amostras coletadas antes do treinamento foram submetidas à mensuração dos hormônios cortisol e testosterona e as amostras após o treinamento apenas à dosagem de cortisol. Iniciou-se uma nova sequência de coleta para dosar e avaliar a testosterona. Ambos os hormônios foram mensurados pelo método de radioimunoensaio. A análise estatística para comparação de cortisol e testosterona, assim como para o perímetro escrotal e testosterona foi realizada através da comparação de Person, com nível de 5% de significância, através do Action 3.1 versão R 3.0.2 (Campinas, SP, Brasil). A dosagem de cortisol sérica antes e após o treinamento resultou em correlação positiva (0,071), demonstrando diferença estatística (p=0,0004) nesses dois momentos avaliados. A comparação entre a testosterona do primeiro dia e o cortisol antes do treinamento foi negativa assim como a testosterona do segundo dia com o cortisol após treinamento. Conclui-se que houve evidência de estresse após o treinamento sem interferência na produção de testosterona.

Bulls in training (n = 17) for rodeo were evaluated for stress interference in testosterone production. Parameter analysis was performed regarding the health of the bulls before training and blood collection. After the exercise, the second blood collection was performed. The samples collected before the training were submitted to the measurement of cortisol and testosterone hormones and the samples after the training only to the cortisol dosage. A new collection sequence was started for dosing and evaluating testosterone. Both hormones were measured by the radioimmunoassay method. The statistical analysis for comparison of cortisol and testosterone, as well as for the scrotal perimeter and testosterone was performed by Pearson correlation with a 5% level of significance through Action 3.1 version R 3.0.2 (Campinas, SP, Brazil). Serum cortisol dosage before and after training resulted in a positive correlation (0.071), showing statistical difference (p = 0.0004) in these two moments evaluated. The comparison between first day testosterone and cortisol before training was negative as was testosterone on the second day with cortisol after training. It was concluded that there was evidence of post-training stress without interference in the production of testosterone

Assuntos

RESUMO

Touros em treinamento (n=17) para rodeio foram avaliados quanto a interferência do estresse na produção de testosterona. Foi realizada análise de parâmetros quanto a higidez dos touros antes do treinamento e coleta de sangue. Após o treinamento, foi realizada a segunda coleta de sangue. As amostras coletadas antes do treinamento foram submetidas à mensuração dos hormônios cortisol e testosterona e as amostras após o treinamento apenas à dosagem de cortisol. Iniciou-se uma nova sequência de coleta para dosar e avaliar a testosterona. Ambos os hormônios foram mensurados pelo método de radioimunoensaio. A análise estatística para comparação de cortisol e testosterona, assim como para o perímetro escrotal e testosterona foi realizada através da comparação de Person, com nível de 5% de significância, através do Action 3.1 versão R 3.0.2 (Campinas, SP, Brasil). A dosagem de cortisol sérica antes e após o treinamento resultou em correlação positiva (0,071), demonstrando diferença estatística (p=0,0004) nesses dois momentos avaliados. A comparação entre a testosterona do primeiro dia e o cortisol antes do treinamento foi negativa assim como a testosterona do segundo dia com o cortisol após treinamento. Conclui-se que houve evidência de estresse após o treinamento sem interferência na produção de testosterona.(AU)

Bulls in training (n = 17) for rodeo were evaluated for stress interference in testosterone production. Parameter analysis was performed regarding the health of the bulls before training and blood collection. After the exercise, the second blood collection was performed. The samples collected before the training were submitted to the measurement of cortisol and testosterone hormones and the samples after the training only to the cortisol dosage. A new collection sequence was started for dosing and evaluating testosterone. Both hormones were measured by the radioimmunoassay method. The statistical analysis for comparison of cortisol and testosterone, as well as for the scrotal perimeter and testosterone was performed by Pearson correlation with a 5% level of significance through Action 3.1 version R 3.0.2 (Campinas, SP, Brazil). Serum cortisol dosage before and after training resulted in a positive correlation (0.071), showing statistical difference (p = 0.0004) in these two moments evaluated. The comparison between first day testosterone and cortisol before training was negative as was testosterone on the second day with cortisol after training. It was concluded that there was evidence of post-training stress without interference in the production of testosterone(AU)

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The immunogenicity and protective efficacy of various antigen-adjuvant formulations derived either from the merozoite-surface protein-3 (MSP-3) or the glutamate-rich protein (GLURP) of Plasmodium falciparum were evaluated in Saimiri sciureus monkeys. These proteins were selected for immunogenicity studies based primarily on their capacity of inducing an antibody-dependent cellular inhibition effect on parasite growth. Some of the S. sciureus monkeys immunized with MSP-3(212-380)-AS02 or GLURP(27-500)-alum were able to fully or partially control parasitaemia upon an experimental P. falciparum [Falciparum Uganda Palo Alto (FUP-SP) strain] blood-stage infection, and this protection was related to the prechallenge antibody titres induced. The data are indicative that MSP-3 and GLURP can induce protective immunity against an experimental P. falciparum infection using adjuvants that are acceptable for human use and this should trigger further studies with those new antigens.

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Angiostrongylus costaricensis is a nematode parasite of wild rodents in the Americas. Man may become infected accidentally and, sometimes, suffers a very severe abdominal disease. Ingestion of raw vegetables has been proven to be a risk factor for the acquisition of A. costaricensis and, therefore, prophylaxis should include food disinfection. The larvicidal effect of wine vinegar, saturated cooking salt (SS) and a 1.5% bleach solution (BW) were compared with a 1-h-incubation period, at room temperature. Larval viability was tested through inoculation in Swiss mice. Only one out of 560 larvae treated with BW (97.3% of the animals were uninfected) was recovered as an adult worm, while 90/336 and 29/512 larvae treated, respectively, with SS and WV were recovered as adult worms. This larvicidal effect of BW was seen also in incubation times as short as 15 min. In conclusion, the 1.5% bleach solution may be helpful for prophylaxis of human abdominal angiostrongyliasis through disinfection of raw vegetables and unpeeled fruits.

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RESUMO

There is a high prevalence of accidental human infection with Angiostrongylus costaricensis in some areas in southern Brazil and sometimes it presents as severe intestinal disease. Prophylaxis is important since there is no medical treatment for the disease. The ingestion of fruits and vegetables contaminated with the mucous secretion of infected molluscs (the intermediate hosts) is one of the proposed modes of transmission. Third stage larvae were incubated at 5 degrees C for 12 hours, in solutions of saturated sodium chloride, vinegar and sodium hypochlorite 1.5%. The larvae had their viability tested through inoculation into albino mice. The percentage of larvae that established infection were 0% in the group treated with sodium hypochloride, 1.8% with NaCl and 2.4% with vinegar. In conclusion, all substances tested reduced the population of viable larvae and may be useful in food decontamination, as a prophylactic measure for abdominal angiostrongylosis.

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