Morphological Studies on the Testis, Epididymis and Vas Deferens of Al-Ahsa Native Rooster

This study was carried out to investigate the morphological and histological structures of the testis, epididymis and vas deferens of the Al-Ahsa native rooster (ANR). There were two types of ANR; the brown feather one with light yellow shank and the black feather one with grey or dark grey shank. Their body weight was 1840.88± 92.13 g and 1555.66± 82.83g, respectively. The morphology of the testes showed that the black rooster has larger testes than the brown rooster and there was asymmetry in size between the right and left testis in both. They were grey yellowish in color and oval-shaped, situated in the abdomen dorsal to the proventriculus, the liver and the gizzard, cranial to the lungs, caudal to the abdominal sac and ventral to the kidneys. The histology of the testes revealed the capsule, the different cells of the lining epithelium of the seminiferous tubules and the interstitial tissue. The morphology of the epididymis was revealed pseudostratified columnar epithelium, light brown in color with c to L-shaped, located cranial to the testis and extended caudally to continue with vas deferens. The latter has columnar epithelium, light grey in color, run caudally medial to the kidneys and opened in the cloaca.(AU)

Seasonal variations of male reproductive parameters of Tomodon dorsatus from Southeastern Brazil / Variações sazonais dos parâmetros reprodutivos do macho de Tomodon dorsatus do sudeste brasileiro

The morphology of the male reproductive tract of Tomodon dorsatus was described in the austral seasons of the year considering macroscopic and microscopic variables. For this purpose, 56 specimens from the herpetological collection of the "Instituto Butantan" were used. Fragments of the testes, kidneys and ductus deferens were collected and submitted to histological routine. The peak of the testicular volume was observed in the summer and the epithelium of the seminiferous tubules had higher height in the summer (p=0.001). The testes were active throughout the year, however, the spermiogenesis peaked in the summer. There were spermatozoa in the lumen of the ductus deferens in all seasons of the year. Renal length was higher in autumn (p=0.027), and renal width did not show a significant increase (p=0.237). The diameter and epithelial height of the sexual segment of the kidney (SSK) showed hypertrophy in winter and spring, coinciding with the mating period. Based on findings of this study, we can suggest that, at the population level, the reproductive cycle of T. dorsatus can be considered seasonal semi-synchronous, due to the peak of spermiogenic activity in the hot season, and discontinuous at the individual level.(AU)

A morfologia do trato reprodutivo do macho de Tomodon dorsatus foi descrita nas estações climáticas do ano com base em variáveis macroscópicas e microscópicas. Para isto, foram usados 56 espécimes oriundos da coleção herpetológica do Instituto Butantan. Fragmentos dos testículos, rins e ductos deferentes foram coletados e submetidos à rotina histológica. O volume testicular foi maior no verão e o epitélio dos túbulos seminíferos mostrou uma maior altura no verão (p=0.001). Os testículos estavam ativos durante todo o ano, contudo, a espermiogênese foi maior no verão. Espermatozoides foram encontrados no lúmen do ducto deferente em todas as estações do ano. O comprimento renal foi maior no outono (p=0.027), e a largura renal não mostrou um aumento significativo (p=0.237). O diâmetro e a altura epitelial do segmento sexual do rim (SSR) mostrou hipertrofia nas estações inverno e primavera, coincidindo com o período reprodutivo. Com base nestes resultados, pode-se sugerir que, em nível populacional, o ciclo reprodutivo de T. dorsatus possa ser considerado semi-sincrônico sazonal, devido à atividade espermiogênica na estação quente, e descontínuo em nível individual.(AU)

Seasonal variations of male reproductive parameters of Tomodon dorsatus from Southeastern Brazil / Variações sazonais dos parâmetros reprodutivos do macho de Tomodon dorsatus do sudeste brasileiro

The morphology of the male reproductive tract of Tomodon dorsatus was described in the austral seasons of the year considering macroscopic and microscopic variables. For this purpose, 56 specimens from the herpetological collection of the "Instituto Butantan" were used. Fragments of the testes, kidneys and ductus deferens were collected and submitted to histological routine. The peak of the testicular volume was observed in the summer and the epithelium of the seminiferous tubules had higher height in the summer (p=0.001). The testes were active throughout the year, however, the spermiogenesis peaked in the summer. There were spermatozoa in the lumen of the ductus deferens in all seasons of the year. Renal length was higher in autumn (p=0.027), and renal width did not show a significant increase (p=0.237). The diameter and epithelial height of the sexual segment of the kidney (SSK) showed hypertrophy in winter and spring, coinciding with the mating period. Based on findings of this study, we can suggest that, at the population level, the reproductive cycle of T. dorsatus can be considered seasonal semi-synchronous, due to the peak of spermiogenic activity in the hot season, and discontinuous at the individual level.(AU)

A morfologia do trato reprodutivo do macho de Tomodon dorsatus foi descrita nas estações climáticas do ano com base em variáveis macroscópicas e microscópicas. Para isto, foram usados 56 espécimes oriundos da coleção herpetológica do Instituto Butantan. Fragmentos dos testículos, rins e ductos deferentes foram coletados e submetidos à rotina histológica. O volume testicular foi maior no verão e o epitélio dos túbulos seminíferos mostrou uma maior altura no verão (p=0.001). Os testículos estavam ativos durante todo o ano, contudo, a espermiogênese foi maior no verão. Espermatozoides foram encontrados no lúmen do ducto deferente em todas as estações do ano. O comprimento renal foi maior no outono (p=0.027), e a largura renal não mostrou um aumento significativo (p=0.237). O diâmetro e a altura epitelial do segmento sexual do rim (SSR) mostrou hipertrofia nas estações inverno e primavera, coincidindo com o período reprodutivo. Com base nestes resultados, pode-se sugerir que, em nível populacional, o ciclo reprodutivo de T. dorsatus possa ser considerado semi-sincrônico sazonal, devido à atividade espermiogênica na estação quente, e descontínuo em nível individual.(AU)

Seasonal variations of male reproductive parameters of Tomodon dorsatus from Southeastern Brazil

ABSTRACT: The morphology of the male reproductive tract of Tomodon dorsatus was described in the austral seasons of the year considering macroscopic and microscopic variables. For this purpose, 56 specimens from the herpetological collection of the Instituto Butantan were used. Fragments of the testes, kidneys and ductus deferens were collected and submitted to histological routine. The peak of the testicular volume was observed in the summer and the epithelium of the seminiferous tubules had higher height in the summer (p=0.001). The testes were active throughout the year, however, the spermiogenesis peaked in the summer. There were spermatozoa in the lumen of the ductus deferens in all seasons of the year. Renal length was higher in autumn (p=0.027), and renal width did not show a significant increase (p=0.237). The diameter and epithelial height of the sexual segment of the kidney (SSK) showed hypertrophy in winter and spring, coinciding with the mating period. Based on findings of this study, we can suggest that, at the population level, the reproductive cycle of T. dorsatus can be considered seasonal semi-synchronous, due to the peak of spermiogenic activity in the hot season, and discontinuous at the individual level.

RESUMO: A morfologia do trato reprodutivo do macho de Tomodon dorsatus foi descrita nas estações climáticas do ano com base em variáveis macroscópicas e microscópicas. Para isto, foram usados 56 espécimes oriundos da coleção herpetológica do Instituto Butantan. Fragmentos dos testículos, rins e ductos deferentes foram coletados e submetidos à rotina histológica. O volume testicular foi maior no verão e o epitélio dos túbulos seminíferos mostrou uma maior altura no verão (p=0.001). Os testículos estavam ativos durante todo o ano, contudo, a espermiogênese foi maior no verão. Espermatozoides foram encontrados no lúmen do ducto deferente em todas as estações do ano. O comprimento renal foi maior no outono (p=0.027), e a largura renal não mostrou um aumento significativo (p=0.237). O diâmetro e a altura epitelial do segmento sexual do rim (SSR) mostrou hipertrofia nas estações inverno e primavera, coincidindo com o período reprodutivo. Com base nestes resultados, pode-se sugerir que, em nível populacional, o ciclo reprodutivo de T. dorsatus possa ser considerado semi-sincrônico sazonal, devido à atividade espermiogênica na estação quente, e descontínuo em nível individual.

Does a bilateral polypropylene mesh alter the duct deferens morphology, testicular size and testosterone levels? Experimental study in rats

Purpose To evaluate the effect of a PP mesh on duct deferens morphology, testicular size and testosterone levels. Methods Forty adult male rats were distributed into groups: 1) no surgery; 2) inguinotomy; 3) mesh placed on the duct deferens; and 4) mesh placed on the spermatic funiculus. After 90 postoperative days, the inguinal region was resected, and blood samples were collected for the measurement of serum testosterone (pg/dl). The ducts deferens were sectioned in three axial sections according to the relationship with the mesh — cranial, medial and caudal. The wall thickness and duct deferens lumen area were measured. Results The morphology of the duct deferens was preserved in all groups. The mesh placement did not alter this morphology in any of the analyzed segments. Surgery, with or without mesh placement, did not alter the morphology, wall thickness or lumen area (p>0.05). In all operated groups, serum testosterone levels were similar (p>0.05) but there was a decrease in testicle size (p<0.05). Conclusion Surgery, with or without mesh placement, did not alter the morphology of the duct deferens and, although this treatment resulted in testicular size reduction, it did not affect serum testosterone levels.(AU)

Does a bilateral polypropylene mesh alter the duct deferens morphology, testicular size and testosterone levels?: experimental study in rats

Purpose To evaluate the effect of a PP mesh on duct deferens morphology, testicular size and testosterone levels. Methods Forty adult male rats were distributed into groups: 1) no surgery; 2) inguinotomy; 3) mesh placed on the duct deferens; and 4) mesh placed on the spermatic funiculus. After 90 postoperative days, the inguinal region was resected, and blood samples were collected for the measurement of serum testosterone (pg/dl). The ducts deferens were sectioned in three axial sections according to the relationship with the mesh cranial, medial and caudal. The wall thickness and duct deferens lumen area were measured. Results The morphology of the duct deferens was preserved in all groups. The mesh placement did not alter this morphology in any of the analyzed segments. Surgery, with or without mesh placement, did not alter the morphology, wall thickness or lumen area (p>0.05). In all operated groups, serum testosterone levels were similar (p>0.05) but there was a decrease in testicle size (p 0.05). Conclusion Surgery, with or without mesh placement, did not alter the morphology of the duct deferens and, although this treatment resulted in testicular size reduction, it did not affect serum testosterone levels.(AU)

Effect of refrigeration at -1°C on spermatozoa quality of domestic cats / Efeito da refrigeração a -1°C na qualidade de espermatozoides de gatos domésticos

The objective of this study was to evaluate the sperm quality obtained of domestic cats by electroejaculation and recovery of the tail of the epididymis after cooling at -1°C and 4°C for 24 and 48 hours. Twenty-nine adult cats (2 to 6kg) were used. Sperm collection was performed by electroejaculation (EEJ), and after 48 hours, the cats were orchiectomized, and sperm sample was obtained from the vas deferens and epididymis tail (EPD). The samples were diluted in ACP-117® extender, and the sperm characteristics were evaluated at three different moments: when still fresh, 24 and 48 hours after cooling. The objective of this study was to evaluate the sperm quality obtained of domestic cats by electroejaculation and recovery of the tail of the epididymis after cooling at -1°C and 4°C for 24 and 48 hours. Twenty-nine adult cats (2 to 6kg) were used. Sperm collection was performed by electroejaculation (EEJ), and after 48 hours, the cats were orchiectomized, and sperm sample was obtained from the vas deferens and epididymis tail (EPD). The samples were diluted in ACP-117® extender, and the sperm characteristics were evaluated at three different moments: when still fresh, 24 and 48 hours after cooling. In order to compare the two refrigeration temperatures, the first stage was to analyze if there was a difference between the harvesting techniques. After this, two experiments were conducted: in the first, sperm sample from 14 cats were used and the cooling was performed at -1°C; and in the second, sample from 15 cats were used and the sperm were refrigerated at 4°C. Sperm kinetics were evaluated by computerized analysis (CASA) and concentration by Neubauer chamber, spermatic morphology was evaluated by modified Karras staining, and membrane integrity was evaluated by eosin nigrosine. The results obtained were analyzed in R software, version 3.2.5 using the Mann-Whitney test for variables with abnormal distributions, considering significance at the level of 5%...(AU)

O objetivo deste trabalho foi avaliar a qualidade espermática de gatos domésticos obtidos por eletroejaculação e recuperação da cauda do epidídimo após a refrigeração a -1°C e a 4°C por 24 e 48 horas. Vinte e nove gatos adultos (2 a 6kg) foram utilizados. A colheita de espermatozoides foi realizada por eletroejaculação (EEJ) e, após 48 horas, os gatos foram orquiectomizados, e as amostras espermáticas foram obtidas a partir do ducto deferente e da cauda do epidídimo (EPD). As amostras foram diluídas em ACP-117® e as características espermáticas foram avaliadas em três momentos distintos: fresco, 24 e 48 horas após a refrigeração. Para ser possível comparar as duas temperaturas de refrigeração, a primeira etapa foi analisar se havia diferença entre as técnicas de colheita. Após isto, dois experimentos foram conduzidos: no primeiro, espermatozoides de 14 gatos foram utilizados e a refrigeração foi realizada a -1°C; e no segundo, amostras de 15 gatos foram utilizados e os espermatozoides foram refrigerados a 4°C. A cinética espermática foi avaliada por análise computadorizada (CASA), a concentração por câmara de Neubauer, a morfologia espermática foi avaliada pela coloração de Karras modificada, e a integridade da membrana foi avaliada por eosina nigrosina. Os resultados obtidos foram analisados no software R, versão 3.2.5, utilizando o teste de Mann-Whitney para variáveis com distribuições anormais, considerando significância ao nível de 5%...(AU)

Effect of refrigeration at -1°C on spermatozoa quality of domestic cats / Efeito da refrigeração a -1°C na qualidade de espermatozoides de gatos domésticos

The objective of this study was to evaluate the sperm quality obtained of domestic cats by electroejaculation and recovery of the tail of the epididymis after cooling at -1°C and 4°C for 24 and 48 hours. Twenty-nine adult cats (2 to 6kg) were used. Sperm collection was performed by electroejaculation (EEJ), and after 48 hours, the cats were orchiectomized, and sperm sample was obtained from the vas deferens and epididymis tail (EPD). The samples were diluted in ACP-117® extender, and the sperm characteristics were evaluated at three different moments: when still fresh, 24 and 48 hours after cooling. The objective of this study was to evaluate the sperm quality obtained of domestic cats by electroejaculation and recovery of the tail of the epididymis after cooling at -1°C and 4°C for 24 and 48 hours. Twenty-nine adult cats (2 to 6kg) were used. Sperm collection was performed by electroejaculation (EEJ), and after 48 hours, the cats were orchiectomized, and sperm sample was obtained from the vas deferens and epididymis tail (EPD). The samples were diluted in ACP-117® extender, and the sperm characteristics were evaluated at three different moments: when still fresh, 24 and 48 hours after cooling. In order to compare the two refrigeration temperatures, the first stage was to analyze if there was a difference between the harvesting techniques. After this, two experiments were conducted: in the first, sperm sample from 14 cats were used and the cooling was performed at -1°C; and in the second, sample from 15 cats were used and the sperm were refrigerated at 4°C. Sperm kinetics were evaluated by computerized analysis (CASA) and concentration by Neubauer chamber, spermatic morphology was evaluated by modified Karras staining, and membrane integrity was evaluated by eosin nigrosine. The results obtained were analyzed in R software, version 3.2.5 using the Mann-Whitney test for variables with abnormal distributions, considering significance at the level of 5%. In ejaculate samples, higher values of total morphological defects were observed after 24 and 48 hours of refrigeration at 4°C (P<0.022) compared to refrigeration at -1°C, using Friedman test. To quantify the decrease in sperm quality, parameter reductions were calculated among time points (F-24h/F-48h/24h-48h). In EPD samples, a greater reduction in sperm quality was detected after 24 hours of refrigeration at 4°C, both in motility and sperm kinetics and in the movement and velocity indices, compared to refrigeration at -1°C. Based on the results, it can be concluded that cooling of feline spermatozoa at -1°C for up to 48 hours was efficient in maintaining spermatic quality collected by EEJ and EPD, and it could be an alternative to spermatozoa cryopreservation in domestic felines.(AU)

O objetivo deste trabalho foi avaliar a qualidade espermática de gatos domésticos obtidos por eletroejaculação e recuperação da cauda do epidídimo após a refrigeração a -1°C e a 4°C por 24 e 48 horas. Vinte e nove gatos adultos (2 a 6kg) foram utilizados. A colheita de espermatozoides foi realizada por eletroejaculação (EEJ) e, após 48 horas, os gatos foram orquiectomizados, e as amostras espermáticas foram obtidas a partir do ducto deferente e da cauda do epidídimo (EPD). As amostras foram diluídas em ACP-117® e as características espermáticas foram avaliadas em três momentos distintos: fresco, 24 e 48 horas após a refrigeração. Para ser possível comparar as duas temperaturas de refrigeração, a primeira etapa foi analisar se havia diferença entre as técnicas de colheita. Após isto, dois experimentos foram conduzidos: no primeiro, espermatozoides de 14 gatos foram utilizados e a refrigeração foi realizada a -1°C; e no segundo, amostras de 15 gatos foram utilizados e os espermatozoides foram refrigerados a 4°C. A cinética espermática foi avaliada por análise computadorizada (CASA), a concentração por câmara de Neubauer, a morfologia espermática foi avaliada pela coloração de Karras modificada, e a integridade da membrana foi avaliada por eosina nigrosina. Os resultados obtidos foram analisados no software R, versão 3.2.5, utilizando o teste de Mann-Whitney para variáveis com distribuições anormais, considerando significância ao nível de 5%. No ejaculado, maiores valores de defeitos morfológicos totais foram observados após 24 e 48 horas de refrigeração a 4°C (P<0,022) em comparação com refrigeração a -1°C, usando o teste de Friedman. Para quantificar a diminuição na qualidade espermática, as reduções dos parâmetros foram calculadas entre os pontos de tempo (F-24h/F-48h/24h-48h). Na EPD, uma maior redução na qualidade espermática foi detectada após 24 horas de refrigeração a 4°C, tanto na motilidade e na cinética espermática quanto nos índices de movimento e velocidade, em comparação com a refrigeração a -1°C. Com base nos resultados, pode concluir-se que a refrigeração dos espermatozoides felino a -1°C, até 48 horas, foi eficaz na manutenção da qualidade espermático colhidos por EEJ e EPD, e pode ser uma alternativa para a criopreservação de espermatozoides em felinos domésticos.(AU)

Achados microbiológicos, moleculares e histopatológicos em pequenos ruminantes experimentalmente infectados com Actinobacillus seminis

ABSTRACT: The aim of this study was to evaluate, in sheep, the pathogenicity of an Actinobacillus seminis strain isolated from a goat in Brazil. Samples of semen, puncture and fragments of epididymis, deferent duct, testicles and seminal vesicles from two goats (animals 1 and 2) and two sheep (animals 3 and 4) were used, and histopathological, microbiological culture and molecular diagnoses were performed. The inoculum was prepared with saline solution at 10-2 dilution corresponding to 1.0 McFarland standard, with A. seminis colonies previously cultured and administered on 2mL volume by intra-preputial (animals 1 and 3) and epididymis tail (animals 2 and 4) routes. At clinical evaluation it were found unilateral swelling of firm consistency after 30 days in epididymis and testicle from animal 4 that continued until the day of euthanasia, as well as animal 1 shown discrete unilateral swelling of testicles. Gross and microscopic lesions in animals 3 and 4 were compatibles with that caused by A. seminis infection. A. seminis was isolated from material of puncture and semen of one sheep (animal 4). It is concluded that the experimental infection model using goats and sheep has proved the pathogenicity of the A. seminis strain isolated from a goat in the Brazilian semiarid and reproduced in a sheep, which confirm the prediletion of the agent for epididymis, with clinical signs, histopathological findings, bacterial isolation and positive molecular diagnosis.

RESUMO: O objetivo deste trabalho foi avaliar a patogenicidade, em ovinos, de uma cepa de Actinobacillus seminis isolada de caprino no Brasil. Foram utilizadas amostras de sêmen, punção e fragmentos de epidídimo, ducto deferente, testículos e glândulas seminíferas de dois caprinos (animais 1 e 2) e dois ovinos (animais 3 e 4), e foram realizados exame histopatológico, cultivo microbiológico e diagnóstico molecular. O inóculo foi preparado com solução salina na diluição de 10-2 correspondendo ao padrão 1,0 da escala de McFarland, com colônias previamente cultivadas de A. seminis e administrado no volume de 2 mL pelas vias intra-prepucial (animais 1 e 3) e na cauda do epidídimo (animais 2 e 4). Na avaliação clínica observou-se aumento unilateral de consistência firme após 30 dias no epidídimo e testículo do animal 4 que continuou até o dia da eutanásia, bem como o animal 1 apresentou discreto aumento unilateral dos testículos. As lesões macroscópicas e microscópicas observadas nos animais 3 e 4 foram compatíveis com aquelas causadas pela infecção por A. seminis. A. seminis foi isolado de material de punção e sêmen de um ovino (animal 4). Conclui-se que o modelo de infecção experimental utilizando caprinos e ovinos comprovou a patogenicidade da amostra de A. seminis, isolada de um caprino no semiárido brasileiro e reproduzida em um ovino, comprovando a predileção do agente pelo epidídimo, com quadro clinico, achados histopatológicos, isolamento bacteriano e diagnóstico molecular positivo.

Achados microbiológicos, moleculares e histopatológicos em pequenos ruminantes experimentalmente infectados com Actinobacillus seminis / Microbiological, molecular and histopathological findings in small ruminants experimentally infected with Actinobacillus seminis

O objetivo deste trabalho foi avaliar a patogenicidade, em ovinos, de uma cepa de Actinobacillus seminis isolada de caprino no Brasil. Foram utilizadas amostras de sêmen, punção e fragmentos de epidídimo, ducto deferente, testículos e glândulas seminíferas de dois caprinos (animais 1 e 2) e dois ovinos (animais 3 e 4), e foram realizados exame histopatológico, cultivo microbiológico e diagnóstico molecular. O inóculo foi preparado com solução salina na diluição de 10-2 correspondendo ao padrão 1,0 da escala de McFarland, com colônias previamente cultivadas de A. seminis e administrado no volume de 2 mL pelas vias intra-prepucial (animais 1 e 3) e na cauda do epidídimo (animais 2 e 4). Na avaliação clínica observou-se aumento unilateral de consistência firme após 30 dias no epidídimo e testículo do animal 4 que continuou até o dia da eutanásia, bem como o animal 1 apresentou discreto aumento unilateral dos testículos. As lesões macroscópicas e microscópicas observadas nos animais 3 e 4 foram compatíveis com aquelas causadas pela infecção por A. seminis. A. seminis foi isolado de material de punção e sêmen de um ovino (animal 4). Conclui-se que o modelo de infecção experimental utilizando caprinos e ovinos comprovou a patogenicidade da amostra de A. seminis, isolada de um caprino no semiárido brasileiro e reproduzida em um ovino, comprovando a predileção do agente pelo epidídimo, com quadro clinico, achados histopatológicos, isolamento bacteriano e diagnóstico molecular positivo.(AU)

The aim of this study was to evaluate, in sheep, the pathogenicity of an Actinobacillus seminis strain isolated from a goat in Brazil. Samples of semen, puncture and fragments of epididymis, deferent duct, testicles and seminal vesicles from two goats (animals 1 and 2) and two sheep (animals 3 and 4) were used, and histopathological, microbiological culture and molecular diagnoses were performed. The inoculum was prepared with saline solution at 10-2 dilution corresponding to 1.0 McFarland standard, with A. seminis colonies previously cultured and administered on 2mL volume by intra-preputial (animals 1 and 3) and epididymis tail (animals 2 and 4) routes. At clinical evaluation it were found unilateral swelling of firm consistency after 30 days in epididymis and testicle from animal 4 that continued until the day of euthanasia, as well as animal 1 shown discrete unilateral swelling of testicles. Gross and microscopic lesions in animals 3 and 4 were compatibles with that caused by A. seminis infection. A. seminis was isolated from material of puncture and semen of one sheep (animal 4). It is concluded that the experimental infection model using goats and sheep has proved the pathogenicity of the A. seminis strain isolated from a goat in the Brazilian semiarid and reproduced in a sheep, which confirm the prediletion of the agent for epididymis, with clinical signs, histopathological findings, bacterial isolation and positive molecular diagnosis.(AU)

Achados microbiológicos, moleculares e histopatológicos em pequenos ruminantes experimentalmente infectados com Actinobacillus seminis / Microbiological, molecular and histopathological findings in small ruminants experimentally infected with Actinobacillus seminis

O objetivo deste trabalho foi avaliar a patogenicidade, em ovinos, de uma cepa de Actinobacillus seminis isolada de caprino no Brasil. Foram utilizadas amostras de sêmen, punção e fragmentos de epidídimo, ducto deferente, testículos e glândulas seminíferas de dois caprinos (animais 1 e 2) e dois ovinos (animais 3 e 4), e foram realizados exame histopatológico, cultivo microbiológico e diagnóstico molecular. O inóculo foi preparado com solução salina na diluição de 10-2 correspondendo ao padrão 1,0 da escala de McFarland, com colônias previamente cultivadas de A. seminis e administrado no volume de 2 mL pelas vias intra-prepucial (animais 1 e 3) e na cauda do epidídimo (animais 2 e 4). Na avaliação clínica observou-se aumento unilateral de consistência firme após 30 dias no epidídimo e testículo do animal 4 que continuou até o dia da eutanásia, bem como o animal 1 apresentou discreto aumento unilateral dos testículos. As lesões macroscópicas e microscópicas observadas nos animais 3 e 4 foram compatíveis com aquelas causadas pela infecção por A. seminis. A. seminis foi isolado de material de punção e sêmen de um ovino (animal 4). Conclui-se que o modelo de infecção experimental utilizando caprinos e ovinos comprovou a patogenicidade da amostra de A. seminis, isolada de um caprino no semiárido brasileiro e reproduzida em um ovino, comprovando a predileção do agente pelo epidídimo, com quadro clinico, achados histopatológicos, isolamento bacteriano e diagnóstico molecular positivo.(AU)

The aim of this study was to evaluate, in sheep, the pathogenicity of an Actinobacillus seminis strain isolated from a goat in Brazil. Samples of semen, puncture and fragments of epididymis, deferent duct, testicles and seminal vesicles from two goats (animals 1 and 2) and two sheep (animals 3 and 4) were used, and histopathological, microbiological culture and molecular diagnoses were performed. The inoculum was prepared with saline solution at 10-2 dilution corresponding to 1.0 McFarland standard, with A. seminis colonies previously cultured and administered on 2mL volume by intra-preputial (animals 1 and 3) and epididymis tail (animals 2 and 4) routes. At clinical evaluation it were found unilateral swelling of firm consistency after 30 days in epididymis and testicle from animal 4 that continued until the day of euthanasia, as well as animal 1 shown discrete unilateral swelling of testicles. Gross and microscopic lesions in animals 3 and 4 were compatibles with that caused by A. seminis infection. A. seminis was isolated from material of puncture and semen of one sheep (animal 4). It is concluded that the experimental infection model using goats and sheep has proved the pathogenicity of the A. seminis strain isolated from a goat in the Brazilian semiarid and reproduced in a sheep, which confirm the prediletion of the agent for epididymis, with clinical signs, histopathological findings, bacterial isolation and positive molecular diagnosis.(AU)

NOVA TÉCNICA DE DEFERENTOPEXIA PRÉ ESCROTAL ASSOCIADO A HERNIORRAFIA PERINEAL NO CÃO EM DECÚBITO DORSAL

Hérnia perineal é descrita como o enfraquecimento muscular da região do períneo, podendo assim ocorrer a migração de vísceras para a região. Ocorre principalmente em cães, machos, não castrados e idosos. Neste estudo objetivou-se descrever uma nova técnica de deferentopexia como método auxiliar na herniorrafia perineal realizada em decúbito dorsal com tração cranial dos membros pélvicos em cães. Foram utilizados 15 cães, machos, inteiros, pesando 17,67 ± 10,28 kg, de diferentes idades e raças, portadores de hérnia perineal. O procedimento cirúrgico consistiu na realização da herniorrafia pelo método tradicional, seguido da realização da orquiectomia pré-escrotal associado a deferentopexia pela confecção de uma amarração entre os dois ductos deferentes de cada testículo através de um nó de cirurgião. Avaliações clínicas foram realizadas no 3º, 15º, 30º e 60º dia pós-cirúrgico. Foram avaliados o comportamento do animal, reações dolorosas a palpação dos pontos de pele, postura ao defecar e urinar e quaisquer complicações relacionadas ao procedimento cirúrgico. Diante dos resultados obtidos, a nova técnica de deferentopexia associado a herniorrafia perineal proporcionou um tempo cirúrgico menor, este realizados em um mesmo decúbito, não apresentando taxa de recidivas nos cães avaliados até o 60º dia pós-operatório, por promover uma menor pressão principalmente da vesícula urinária, próstata e colón sobre o diafragma pélvico, tendo assim menores complicações comparado a técnica padrão.

Perineal hernia is described as the weakening of the muscle in the perineum region, which may result in the migration of viscera to the region. It occurs mainly in dogs, males, nonneutered and elderly. This study aimed to describe a new technique of deferentopexy as an auxiliary method in perineal herniorrhaphy performed in the supine position with cranial traction of the pelvic limbs in dogs. Fifteen dogs, male, whole, weighing 17.67 ± 10.28 kg of different ages and races, with perineal hernia were used. The surgical procedure consisted of performing herniorrhaphy using the traditional method, followed by performing a pre-scrotal orchiectomy associated with deferentopexy by making a tie between the two different ducts of each testis through a surgeon's knot. Clinical evaluations were performed on the 3rd, 15th, 30th and 60th postoperative days. The animal's behavior, painful reactions to palpation of the skin points, posture when defecating and urinating and any complications related to the surgical procedure were evaluated. In view of the results obtained, the new technique of deferentopexy associated with perineal herniorrhaphy provided a shorter surgical time, performed in the same decubitus position, with no recurrence rate in the dogs evaluated until the 60th postoperative day, as it promotes less pressure mainly on the gallbladder urinary, prostate and colon on the pelvic diaphragm, thus having less complications compared to the standard technique.

Vasectomy in spotted paca (Cuniculus paca)

Background: Cuniculus paca is the second largest neotropical rodent. It is not endangered, but your habitat has been destroyed and the specie has been hunted, because of its prized meat. In this context captive breeding is an alternative to reduce the hunt. Then, adult male vasectomy is an interesting alternative for Cuniculus paca since the animal does not lose libido and maintain cyclicity of females into the enclosure. This technique is a method of sterilization which the vas deferens is surgically clamped, cut, or otherwise sealed and thus prevents the release of sperm when a male ejaculates. The aim of this study was to describe the vasectomy technique on a male spotted paca kept in captive. Case: A captive adult male of Cuniculus paca, lived in Brazilian wild fauna breeding for scientific research. It was maintained on precinct with no other animal, ate fruits, vegetables, tubers and rodent chow and water offered ad libitum. It was submitted to bilateral vasectomy to maintain reproductive behavior on bevy, but not impregnate females. The anaesthesia was performed using ketamine hydrochloride (25 mg/kg IM) and midazolam (0.5 mg/kg IM) as premedication, and isoflurane in open system by facemask diluted in 100% O2 for induction and maintenance. Immediately after induction, was performed epidural anesthesia using 4 mg/kg of lidocaine hydrochloride without vasoconstrictor [...]

Vasectomy in spotted paca (Cuniculus paca)

Background: Cuniculus paca is the second largest neotropical rodent. It is not endangered, but your habitat has been destroyed and the specie has been hunted, because of its prized meat. In this context captive breeding is an alternative to reduce the hunt. Then, adult male vasectomy is an interesting alternative for Cuniculus paca since the animal does not lose libido and maintain cyclicity of females into the enclosure. This technique is a method of sterilization which the vas deferens is surgically clamped, cut, or otherwise sealed and thus prevents the release of sperm when a male ejaculates. The aim of this study was to describe the vasectomy technique on a male spotted paca kept in captive. Case: A captive adult male of Cuniculus paca, lived in Brazilian wild fauna breeding for scientific research. It was maintained on precinct with no other animal, ate fruits, vegetables, tubers and rodent chow and water offered ad libitum. It was submitted to bilateral vasectomy to maintain reproductive behavior on bevy, but not impregnate females. The anaesthesia was performed using ketamine hydrochloride (25 mg/kg IM) and midazolam (0.5 mg/kg IM) as premedication, and isoflurane in open system by facemask diluted in 100% O2 for induction and maintenance. Immediately after induction, was performed epidural anesthesia using 4 mg/kg of lidocaine hydrochloride without vasoconstrictor [...](AU)

POTENCIAL EFEITO ESTERILIZANTE DO ÓLEO ESSENCIAL DE CRAVO DA ÍNDIA (Eugenia caryophyllata) EM SUÍNOS POR ADMINISTRAÇÃO INTRATESTICULAR NOS PRIMEIROS DIAS DE VIDA

A proteína animal mais consumida no mundo é a carne suína. O aumento por informações de como se produz a carne, faz parte das queixas dos consumidores, pelas preocupações envolvendo o bem-estar animal. As agroindústrias têm buscado atualizar as técnicas de produção com o intuito de atender os consumidores e melhorar a palatabilidade e o sabor da carne. Um dos objetivos na suinocultura é a ausência de substâncias residuais na carne, oriundas dos hormônios esteroides, naturalmente produzidos a partir do quinto mês de vida, onde se inicia a maturidade sexual e que diminui a qualidade do produto final. As técnicas usuais para castração de suínos estão sendo substituídas por novos modelos, com a finalidade de não causar sofrimento aos animais, dentre elas, a castração química que vem sendo estudada como alternativa para diminuir custos aos produtores, além do que, é considerada técnica de fácil execução e que respeita o bem-estar dos animais. Ao cravo da índia (Eugenia caryophyllata) são atribuídos diferentes potenciais terapêuticos, dentre eles há o relato de ser esterilizante químico. O objetivo deste estudo foi avaliar o potencial efeito esterilizante do óleo de cravo da índia (Eugenia caryophyllata) em suínos, afim de oferecer uma alternativa de baixo custo, facilidade de execução e que sigam as diretrizes do bem-estar animal. Foram selecionados ao acaso 20 suínos, sem raça definida do setor de suinocultura da Universidade Paranaense, divididos em quatros grupos contendo cinco repetições cada. Foram administrados aos sete dias de vida dos animais, inicialmente analgésico meloxicam e anestésico local lidocaína 2% para analgesia preemptiva, e na sequência, óleo de cravo da índia em dois grupos tratamentos nas doses/volume de 0,07mL/kg (G1) e 0,3mL/kg (G3), e solução fisiológica em dois grupos controles no volume de 0,07mL/kg (G2) e 0,3mL/kg (G4), a via de administração foi a intratesticular bilateral em todos os grupos. Após 60 dias os animais foram sedados, anestesiados e então submetidos a orquiectomia bilateral. Os testículos foram coletados para processamento histológico. Os animais foram acompanhados clinicamente durante 10 dias, tendo sido realizada a limpeza das feridas. Nas avaliações histopatológicas, foram observadas as estruturas da túnica albugínea, septos testiculares e lóbulos testiculares neles sendo avaliados as estruturas dos túbulos seminíferos, as células intersticiais e de sustentação. Foram também avaliadas as estruturas do mediastino testicular, rede testicular, ducto deferente e epidídimo. Não foram observadas nenhuma alteração clínica digna de nota, após aplicação do óleo essencial de cravo da índia, como também após ao procedimento de orquiectomia. A histopatologia revelou que nenhum dos agentes utilizados foram capazes de induzir esterilização química dos animais, onde todas as estruturas avaliadas encontravam-se preservadas. Conclui-se que a técnica de castração química testada é de fácil execução, porém, o óleo essencial de cravo não foi capaz de induzir esterilização nos animais no modelo adotado para o estudo, podendo atribuir este resultado a imaturidade dos animais. Sendo assim, acredita-se serem necessários novos estudos para esclarecimentos sobre o agente esclerosante utilizado e se o efeito pode ocorrer quando os animais estiverem entrando na maturidade sexual.

The most consumed animal protein in the world is pork. The increase in information on how meat is produced is part of consumer complaints, concerns about animal welfare. Agro-industries have sought to update production techniques in order to serve consumers and improve the palatability and flavor of meat. One of the objectives in pig farming is the absence of residual substances in the meat, derived from steroid hormones, naturally produced from the fifth month of life, where sexual maturity begins and which reduces the quality of the final product. The usual techniques for pig castration are being replaced by new models, with the purpose of not causing suffering to the animals, among them, the chemical castration that has been studied as an alternative to reduce costs to the producers, besides, it is considered technique of easy execution and that respects the welfare of the animals. The clove (Eugenia caryophyllata) has different therapeutic potentials, among which there is a report of being a chemical sterilizer. The aim of this study was to evaluate the potential sterilizing effect of clove oil (Eugenia caryophyllata) in pigs, in order to offer a low cost alternative, ease of execution and that follow the guidelines of animal welfare. Twenty pigs of mixed breed from the pig industry of the Universidade Paranaense were randomLy selected, divided into four groups containing five replicates each. The animals were administered at seven days of life, initially meloxicam analgesic and 2% lidocaine local anesthetic for preemptive analgesia, and subsequently, clove oil in two treatment groups at doses / volume of 0.07mL/kg (G1) and 0.3mL/kg (G3), and saline solution in two control groups in the volume of 0.07mL/kg (G2) and 0.3mL/kg (G4), the route of administration was bilateral intratesticular in all groups. After 60 days, the animals were sedated and anesthetized and then submitted to bilateral orchiectomy. The testicles were collected for histological processing. The animals were followed up clinically for 10 days and the wounds were cleaned. In histopathological evaluations, the structures of the tunica albuginea, testicular septa and testicular lobes were observed, and the structures of the seminiferous tubules, interstitial and support cells were evaluated. The structures of the testicular mediastinum, testicular network, vas deferens and epididymis were also evaluated. No significant clinical changes were observed after the application of clove essential oil, as well as after the orchiectomy procedure. Histopathology revealed that none of the agents used were able to induce chemical sterilization of the animals, where all the evaluated structures were preserved. It is concluded that the tested chemical castration technique is easy to perform, however, the clove essential oil was not able to induce sterilization in the animals in the model adopted for the study, which may attribute this result to the immaturity of the animals. Therefore, it is believed that further studies are needed to clarify the sclerosing agent used and whether the effect can occur when the animals are entering sexual maturity.

A study on vas deference and seminal vesicle of male goats (Capra hircus)

Background: Reproductive activity of male animal is strongly associated with development of the testicle, the conductor channels and accessory sex gland. Vas deference may be considered the extra-testicular continuation from cauda of the epididymis, and it is the portion of the reproductive tract fundamentally associated with transportation of the sperm-containing fluid from each epididymis to the urethra for their finishing discharge. Non-ampulated part is further divided into: extra-abdominal portion along the caudal border of testes, up to the vaginal ring and abdominal portion started from the vaginal ring to ampullae. Accessory sex glands including vesicular gland and ampullae of vas deferens are characteristically essential for reproductive process. Gross morphometric features of anatomical structures of male reproductive tract in an animal make available a very valuable mechanism in understanding of several physiological and reproductive phenomena. The current study aim at documenting baseline data on gross morphometric aspects of vas deference and seminal vesicle in adult male local nondescript goats in Pakistan ecology that could be utilized as reference values in evaluating their congenital defects and gross pathological abnormalities.Materials, Methods & Results: Experiments were carried out on ampullated and non-ampullated segment of vas deference and seminal vesicle. A total of n = 100 local male goats of 2-3 years of age were selected for this study. Vas deference and seminal vesicles (accessory sex gland) were collected immediately after slaughter from local abattoirs. The non-ampullated segment of vas deference was further divided into abdominal and extra-abdominal segment. Specimens were dissected and washed with normal saline. Standard procedure was adopted for these morphometric features of vas deference and seminal vesicle by using vernier caliper, scale, non-stretchable thread and electronic weighing balance.[...](AU)

A study on vas deference and seminal vesicle of male goats (Capra hircus)

Background: Reproductive activity of male animal is strongly associated with development of the testicle, the conductor channels and accessory sex gland. Vas deference may be considered the extra-testicular continuation from cauda of the epididymis, and it is the portion of the reproductive tract fundamentally associated with transportation of the sperm-containing fluid from each epididymis to the urethra for their finishing discharge. Non-ampulated part is further divided into: extra-abdominal portion along the caudal border of testes, up to the vaginal ring and abdominal portion started from the vaginal ring to ampullae. Accessory sex glands including vesicular gland and ampullae of vas deferens are characteristically essential for reproductive process. Gross morphometric features of anatomical structures of male reproductive tract in an animal make available a very valuable mechanism in understanding of several physiological and reproductive phenomena. The current study aim at documenting baseline data on gross morphometric aspects of vas deference and seminal vesicle in adult male local nondescript goats in Pakistan ecology that could be utilized as reference values in evaluating their congenital defects and gross pathological abnormalities.Materials, Methods & Results: Experiments were carried out on ampullated and non-ampullated segment of vas deference and seminal vesicle. A total of n = 100 local male goats of 2-3 years of age were selected for this study. Vas deference and seminal vesicles (accessory sex gland) were collected immediately after slaughter from local abattoirs. The non-ampullated segment of vas deference was further divided into abdominal and extra-abdominal segment. Specimens were dissected and washed with normal saline. Standard procedure was adopted for these morphometric features of vas deference and seminal vesicle by using vernier caliper, scale, non-stretchable thread and electronic weighing balance.[...]

Morfologia do escroto, do testículo e das vias espermáticas de Metachirus nudicaudatus (Geoffroy, 1803), Didelphidae-Marsupialia

Abstract: Gonads and sperm pathways of five adult male Metachirus nudicaudatus in the reproductive phase were used to describe the morphology of scrotum, testicle, and spermatic tract. M. nudicaudatus has a scrotum pre-penis which contains the testicles permanently. The scrotal skin is not pigmented and has few hairs and glands. The parietal vaginal tunic is slightly pigmented. The testicles are oval and connected to the epididymis by testicular-epididymal pedicle; they are surrounded externally by the testicular capsule and supported by a stroma of connective nature. Interstitial cells are the predominant elements in abundant intertubular tissue. The seminiferous tubules are wide, meandering and surrounded by a fibro-elastic coat, containing myoid cells. The seminiferous epithelium is composed of spermatogenic cells and Sertoli cells interspersed. The seminiferous tubules converge toward the end of the testis capitata, getting coated only support cells, featuring a transition region between the seminiferous tubules and straight tubules, occupied by a type "valve" structure that partially blocks the tubular lumen. Straight tubules together to form a single efferent ductule, which runs a small intra-testicular extent, penetrates through the tunica and the pedicle testis-epididymis. The flexuosa part of the efferent ductule forms a separate lobe in the medial part of the body of the epididymis. The epididymis is enveloped by a capsule and epididymal comprising the epididymal duct, which is quite entangled. The epididymal duct is lined by pseudostratified columnar epithelium with simple principal, basal, apical and "clear halo" cells. The main cells are prevalent and have morphological and histochemical differing characteristics along the duct, enabling to characterize nine different epididymal areas. In the lumen of the seventh area (top of tail) that starts the pairing of sperm. This phenomenon coincides well with morphological change and a larger amount of neutral muco-substances is secreted in that area. Vas deferens has three parts: fair-epididymal, abdominal and funicular part, based on histological and histochemical changes of the epithelium and surrounding components. The vas deferens has no bulb and even crosses the ureter before flowing into the urethra. The spermatic cord contains the vas deferens, testicular artery and veins, lymphatic vessels, nerves and developed cremaster muscle. Its components have structural changes in the proximal, middle and distal region, with a peculiar admirable network.

Resumo: Foram utilizadas as gônadas e vias espermáticas de cinco animais machos, adultos em fase reprodutiva, da espécie Metachirus nudicaudatus Geoffroy 1803, única espécie do gênero, para descrever a morfologia do escroto, do testículo e das vias espermáticas. O Metachirus possui escroto pré-peniano e que contém os testículos permanentemente. A pele escrotal é não pigmentada e com poucos pelos e glândulas. A lâmina parietal da túnica vaginal apresenta-se pouco pigmentada. Os testículos são ovais e ligados ao epidídimo através do pedículo testículo-epididimário. Eles são envolvidos, externamente, pela cápsula testicular e sustentados por um estroma de natureza conjuntiva. As células intersticiais são os elementos predominantes no abundante tecido intertubular. Os túbulos seminíferos são largos, enovelados e envolvidos por uma túnica própria fibroelástica, contendo células mióides. O epitélio seminífero é formado pelas células espermatogênicas e de Sertoli intercaladas. Os túbulos seminíferos convergem em direção à extremidade capitata do testículo, ficando revestidos por apenas células de sustentação, caracterizando uma região de transição entre túbulos seminíferos e túbulos retos, ocupada por uma estrutura tipo "válvula" que obstrui parcialmente o lume tubular. Os túbulos retos reúnem-se para formar um único dúctulo eferente, que percorre uma pequena extensão intratesticular, atravessa a albugínea e penetra no pedículo testículo-epididimário. A parte flexuosa do dúctulo eferente forma um lóbulo separado na parte medial do corpo do epidídimo. O epidídimo é envolvido pela cápsula epididimária e constituído pelo ducto epididimário, que se encontra bastante enovelado. O ducto epididimário é revestido por epitélio simples colunar pseudoestratificado apresentando células principais, basais, apicais e de "halo claro". As células principais são predominantes e apresentam características morfológicas e histoquímicas que diferem ao longo do ducto, possibilitando a caracterização de nove diferentes zonas epididimárias. É no lume da zona sete (início da cauda) que começa o pareamento de espermatozoides. Esse fenômeno coincide com alterações morfológicas bem evidentes e uma maior quantidade de mucossubstâncias neutras é secretada nessa zona.O ducto deferente apresenta-se dividido em três partes: justa-epididimária, funicular e abdominal, baseando nas variações histológicas e histoquímicas de seu epitélio e componentes envolventes. O ducto deferente não apresenta ampola e nem cruza o ureter antes de desembocar na uretra. O funículo espermático contém o ducto deferente, artéria e veias testiculares, vasos linfáticos, nervos e um desenvolvido músculo cremáster. Seus componentes apresentam modificações estruturais nas regiões proximal, média e distal, sendo notável a peculiar rede admirável.

Morfologia do escroto, do testículo e das vias espermáticas de Metachirus nudicaudatus (Geoffroy, 1803), Didelphidae-Marsupialia

Abstract: Gonads and sperm pathways of five adult male Metachirus nudicaudatus in the reproductive phase were used to describe the morphology of scrotum, testicle, and spermatic tract. M. nudicaudatus has a scrotum pre-penis which contains the testicles permanently. The scrotal skin is not pigmented and has few hairs and glands. The parietal vaginal tunic is slightly pigmented. The testicles are oval and connected to the epididymis by testicular-epididymal pedicle; they are surrounded externally by the testicular capsule and supported by a stroma of connective nature. Interstitial cells are the predominant elements in abundant intertubular tissue. The seminiferous tubules are wide, meandering and surrounded by a fibro-elastic coat, containing myoid cells. The seminiferous epithelium is composed of spermatogenic cells and Sertoli cells interspersed. The seminiferous tubules converge toward the end of the testis capitata, getting coated only support cells, featuring a transition region between the seminiferous tubules and straight tubules, occupied by a type "valve" structure that partially blocks the tubular lumen. Straight tubules together to form a single efferent ductule, which runs a small intra-testicular extent, penetrates through the tunica and the pedicle testis-epididymis. The flexuosa part of the efferent ductule forms a separate lobe in the medial part of the body of the epididymis. The epididymis is enveloped by a capsule and epididymal comprising the epididymal duct, which is quite entangled. The epididymal duct is lined by pseudostratified columnar epithelium with simple principal, basal, apical and "clear halo" cells. The main cells are prevalent and have morphological and histochemical differing characteristics along the duct, enabling to characterize nine different epididymal areas. In the lumen of the seventh area (top of tail) that starts the pairing of sperm. This phenomenon coincides well with morphological change and a larger amount of neutral muco-substances is secreted in that area. Vas deferens has three parts: fair-epididymal, abdominal and funicular part, based on histological and histochemical changes of the epithelium and surrounding components. The vas deferens has no bulb and even crosses the ureter before flowing into the urethra. The spermatic cord contains the vas deferens, testicular artery and veins, lymphatic vessels, nerves and developed cremaster muscle. Its components have structural changes in the proximal, middle and distal region, with a peculiar admirable network.

Resumo: Foram utilizadas as gônadas e vias espermáticas de cinco animais machos, adultos em fase reprodutiva, da espécie Metachirus nudicaudatus Geoffroy 1803, única espécie do gênero, para descrever a morfologia do escroto, do testículo e das vias espermáticas. O Metachirus possui escroto pré-peniano e que contém os testículos permanentemente. A pele escrotal é não pigmentada e com poucos pelos e glândulas. A lâmina parietal da túnica vaginal apresenta-se pouco pigmentada. Os testículos são ovais e ligados ao epidídimo através do pedículo testículo-epididimário. Eles são envolvidos, externamente, pela cápsula testicular e sustentados por um estroma de natureza conjuntiva. As células intersticiais são os elementos predominantes no abundante tecido intertubular. Os túbulos seminíferos são largos, enovelados e envolvidos por uma túnica própria fibroelástica, contendo células mióides. O epitélio seminífero é formado pelas células espermatogênicas e de Sertoli intercaladas. Os túbulos seminíferos convergem em direção à extremidade capitata do testículo, ficando revestidos por apenas células de sustentação, caracterizando uma região de transição entre túbulos seminíferos e túbulos retos, ocupada por uma estrutura tipo "válvula" que obstrui parcialmente o lume tubular. Os túbulos retos reúnem-se para formar um único dúctulo eferente, que percorre uma pequena extensão intratesticular, atravessa a albugínea e penetra no pedículo testículo-epididimário. A parte flexuosa do dúctulo eferente forma um lóbulo separado na parte medial do corpo do epidídimo. O epidídimo é envolvido pela cápsula epididimária e constituído pelo ducto epididimário, que se encontra bastante enovelado. O ducto epididimário é revestido por epitélio simples colunar pseudoestratificado apresentando células principais, basais, apicais e de "halo claro". As células principais são predominantes e apresentam características morfológicas e histoquímicas que diferem ao longo do ducto, possibilitando a caracterização de nove diferentes zonas epididimárias. É no lume da zona sete (início da cauda) que começa o pareamento de espermatozoides. Esse fenômeno coincide com alterações morfológicas bem evidentes e uma maior quantidade de mucossubstâncias neutras é secretada nessa zona.O ducto deferente apresenta-se dividido em três partes: justa-epididimária, funicular e abdominal, baseando nas variações histológicas e histoquímicas de seu epitélio e componentes envolventes. O ducto deferente não apresenta ampola e nem cruza o ureter antes de desembocar na uretra. O funículo espermático contém o ducto deferente, artéria e veias testiculares, vasos linfáticos, nervos e um desenvolvido músculo cremáster. Seus componentes apresentam modificações estruturais nas regiões proximal, média e distal, sendo notável a peculiar rede admirável.

Morfologia do escroto, do testículo e das vias espermáticas de Metachirus nudicaudatus (Geoffroy, 1803), Didelphidae-Marsupialia / Morphology of scrotum and testicle, and spermatic pathways of Metachirus nudicaudatus (Geoffroy, 1803), Didelphidae-Marsupialia

Foram utilizadas as gônadas e vias espermáticas de cinco animais machos, adultos em fase reprodutiva, da espécie Metachirus nudicaudatus Geoffroy 1803, única espécie do gênero, para descrever a morfologia do escroto, do testículo e das vias espermáticas. O Metachirus possui escroto pré-peniano e que contém os testículos permanentemente. A pele escrotal é não pigmentada e com poucos pelos e glândulas. A lâmina parietal da túnica vaginal apresenta-se pouco pigmentada. Os testículos são ovais e ligados ao epidídimo através do pedículo testículo-epididimário. Eles são envolvidos, externamente, pela cápsula testicular e sustentados por um estroma de natureza conjuntiva. As células intersticiais são os elementos predominantes no abundante tecido intertubular. Os túbulos seminíferos são largos, enovelados e envolvidos por uma túnica própria fibroelástica, contendo células mióides. O epitélio seminífero é formado pelas células espermatogênicas e de Sertoli intercaladas. Os túbulos seminíferos convergem em direção à extremidade capitata do testículo, ficando revestidos por apenas células de sustentação, caracterizando uma região de transição entre túbulos seminíferos e túbulos retos, ocupada por uma estrutura tipo "válvula" que obstrui parcialmente o lume tubular. Os túbulos retos reúnem-se para formar um único dúctulo eferente, que percorre uma pequena extensão intratesticular, atravessa a albugínea e penetra no pedículo testículo-epididimário. A parte flexuosa do dúctulo eferente forma um lóbulo separado na parte medial do corpo do epidídimo. O epidídimo é envolvido pela cápsula epididimária e constituído pelo ducto epididimário, que se encontra bastante enovelado. O ducto epididimário é revestido por epitélio simples colunar pseudoestratificado apresentando células principais, basais, apicais e de "halo claro". As células principais são predominantes e apresentam características morfológicas e histoquímicas que diferem ao longo do ducto, possibilitando a caracterização de nove diferentes zonas epididimárias. É no lume da zona sete (início da cauda) que começa o pareamento de espermatozoides. Esse fenômeno coincide com alterações morfológicas bem evidentes e uma maior quantidade de mucossubstâncias neutras é secretada nessa zona.O ducto deferente apresenta-se dividido em três partes: justa-epididimária, funicular e abdominal, baseando nas variações histológicas e histoquímicas de seu epitélio e componentes envolventes. O ducto deferente não apresenta ampola e nem cruza o ureter antes de desembocar na uretra. O funículo espermático contém o ducto deferente, artéria e veias testiculares, vasos linfáticos, nervos e um desenvolvido músculo cremáster. Seus componentes apresentam modificações estruturais nas regiões proximal, média e distal, sendo notável a peculiar rede admirável.(AU)

Gonads and sperm pathways of five adult male Metachirus nudicaudatus in the reproductive phase were used to describe the morphology of scrotum, testicle, and spermatic tract. M. nudicaudatus has a scrotum pre-penis which contains the testicles permanently. The scrotal skin is not pigmented and has few hairs and glands. The parietal vaginal tunic is slightly pigmented. The testicles are oval and connected to the epididymis by testicular-epididymal pedicle; they are surrounded externally by the testicular capsule and supported by a stroma of connective nature. Interstitial cells are the predominant elements in abundant intertubular tissue. The seminiferous tubules are wide, meandering and surrounded by a fibro-elastic coat, containing myoid cells. The seminiferous epithelium is composed of spermatogenic cells and Sertoli cells interspersed. The seminiferous tubules converge toward the end of the testis capitata, getting coated only support cells, featuring a transition region between the seminiferous tubules and straight tubules, occupied by a type "valve" structure that partially blocks the tubular lumen. Straight tubules together to form a single efferent ductule, which runs a small intra-testicular extent, penetrates through the tunica and the pedicle testis-epididymis. The flexuosa part of the efferent ductule forms a separate lobe in the medial part of the body of the epididymis. The epididymis is enveloped by a capsule and epididymal comprising the epididymal duct, which is quite entangled. The epididymal duct is lined by pseudostratified columnar epithelium with simple principal, basal, apical and "clear halo" cells. The main cells are prevalent and have morphological and histochemical differing characteristics along the duct, enabling to characterize nine different epididymal areas. In the lumen of the seventh area (top of tail) that starts the pairing of sperm. This phenomenon coincides well with morphological change and a larger amount of neutral muco-substances is secreted in that area. Vas deferens has three parts: fair-epididymal, abdominal and funicular part, based on histological and histochemical changes of the epithelium and surrounding components. The vas deferens has no bulb and even crosses the ureter before flowing into the urethra. The spermatic cord contains the vas deferens, testicular artery and veins, lymphatic vessels, nerves and developed cremaster muscle. Its components have structural changes in the proximal, middle and distal region, with a peculiar admirable network.(AU)