Assessment of coconut water added to Numida meleagris egg yolk as cryoprotectant for goat semen

Effects were assessed of the dilutants TRIS and ACP - 101c® with the addition of different guinea fowl (Numida meleagris) egg yolk concentrations. Fifteen ejaculates were collected from five goats of the Anglo Nubian breed. The ejaculates were pooled and then divided into 12 groups, two control groups (GC1 TRIS, with 2.5% Gallus gallus domesticus hen egg yolk GOGD), (GC2 Control Group ACP - 101c®, with the addition of 2.5% Gallus gallus domesticus hen egg yolk GOGD) and ten experimental groups (EG), containing TRIS and ACP added with different concentrations of egg yolk from guinea hen (Numida meleagris) (TRIS 2,5% GONM; TRIS 5% GONM; TRIS 10% GONM; TRIS 15% GONM; TRIS 20% GONM; ACP® 2,5% GONM; ACP® 5% GONM; ACP® 10% GONM; ACP® 15% GONM; ACP® 20% GONM). Then cryopreservation was carried out and the samples stored in liquid nitrogen (-196 °C). After seven days, the samples were thawed and assessed for spermatic kinetics, immunofluorescence and sperm morphology. Analysis of GOMN by the CASA system showed that the various parameters were similar to those of GOGD (P>0.05). The membrane integrity, mitochondrial potential and the acrosome were not influenced by the treatment (P>0.05) nor by the dilutant used for cryopreservation (P>0.05). The spermatic morphology was also preserved by the different GOGD and GONM concentrations in the ACP® and TRIS dilutants, with no statistically significant differences (P<0.05). It was concluded that Numida meleagris egg yolk, as external membrane cryoproctant added to the dilutants ACP-101c® and TRIS, improved goat semen quality.(AU)

Desafios e perspectivas na produção in vivo de embriões de pequenos ruminantes no Nordeste do Brasil / Challenges and perspectives in the in vivo production of small ruminant embryos in northeast of Brazil

Em decorrência da necessidade de aproveitamento de matrizes e reprodutores de alto mérito genético biotecnologias reprodutivas como a Multipla Ovulação e Transferência de Embriões (MOTE) vêm sendo cada vez mais utilizada, garantindo assim a produtividade mesmo diante de obstáculos. Nos últimos anos essa atividade vem apresentando um acentuado desenvolvimento e aprimoramento, principalmente em caprinos e ovinos que se constituem espécies de extrema importância para a Região Nordeste do Brasil, por serem uma das culturas mais vantajosas quando comparado com as demais culturas como a pecuária e por se tratar de uma atividade sustentável do ponto de vista ambiental, sociocultural e econômico. Dentre os principais fatores que ainda afetam o desempenho e sucesso dos programas de Transferência de Embriões (TE) em pequenos ruminantes podemos destacar a seleção de fêmeas doadoras e receptoras, variabilidade de resposta aos protocolos de superovulação, regressão prematura de corpo lúteo (CL), necessidade de etapas cirúrgicas como a laparotomia e laparoscopia e baixa disponibilidade de mão de obra especializada. Nesse sentido, este artigo aborda as principais etapas da produção in vivo de embriões em pequenos ruminantes bem como os desafios e as perspectivas de cada etapa a serem enfrentadas na Região Nordeste do Brasil.

As a result of the need to use matrices and breeders with high genetic merit, reproductive biotechnologies such as Multiple Ovulation and Embryo Transfer (MOTE) have been increasingly used, thus guaranteeing productivity even in the face of obstacles. In recent years, this activity has shown a marked development and improvement, especially in goats and sheep, which are extremely important species for the Northeast Region of Brazil, as they are one of the most advantageous crops for this region when compared to other crops such as livestock and because it is a sustainable activity from an environmental, socio-cultural and economic point of view. Among the main factors that still affect the performance and success of Embryo Transfer (ET) programs in small ruminants we can highlight the selection of donor and recipient females, variability in response to superovulation protocols, premature corpus luteum (CL) regression, need for surgical steps such as laparotomy and laparoscopy and low availability of specialized labor. In this sense, this article addresses the main stages of invivo embryo production in small ruminants as well as the challenges and perspectives of each stage to be faced in the Northeast Region of Brazil.

Desafios e perspectivas na produção in vivo de embriões de pequenos ruminantes no Nordeste do Brasil / Challenges and perspectives in the in vivo production of small ruminant embryos in northeast of Brazil

Em decorrência da necessidade de aproveitamento de matrizes e reprodutores de alto mérito genético biotecnologias reprodutivas como a Multipla Ovulação e Transferência de Embriões (MOTE) vêm sendo cada vez mais utilizada, garantindo assim a produtividade mesmo diante de obstáculos. Nos últimos anos essa atividade vem apresentando um acentuado desenvolvimento e aprimoramento, principalmente em caprinos e ovinos que se constituem espécies de extrema importância para a Região Nordeste do Brasil, por serem uma das culturas mais vantajosas quando comparado com as demais culturas como a pecuária e por se tratar de uma atividade sustentável do ponto de vista ambiental, sociocultural e econômico. Dentre os principais fatores que ainda afetam o desempenho e sucesso dos programas de Transferência de Embriões (TE) em pequenos ruminantes podemos destacar a seleção de fêmeas doadoras e receptoras, variabilidade de resposta aos protocolos de superovulação, regressão prematura de corpo lúteo (CL), necessidade de etapas cirúrgicas como a laparotomia e laparoscopia e baixa disponibilidade de mão de obra especializada. Nesse sentido, este artigo aborda as principais etapas da produção in vivo de embriões em pequenos ruminantes bem como os desafios e as perspectivas de cada etapa a serem enfrentadas na Região Nordeste do Brasil.(AU)

As a result of the need to use matrices and breeders with high genetic merit, reproductive biotechnologies such as Multiple Ovulation and Embryo Transfer (MOTE) have been increasingly used, thus guaranteeing productivity even in the face of obstacles. In recent years, this activity has shown a marked development and improvement, especially in goats and sheep, which are extremely important species for the Northeast Region of Brazil, as they are one of the most advantageous crops for this region when compared to other crops such as livestock and because it is a sustainable activity from an environmental, socio-cultural and economic point of view. Among the main factors that still affect the performance and success of Embryo Transfer (ET) programs in small ruminants we can highlight the selection of donor and recipient females, variability in response to superovulation protocols, premature corpus luteum (CL) regression, need for surgical steps such as laparotomy and laparoscopy and low availability of specialized labor. In this sense, this article addresses the main stages of invivo embryo production in small ruminants as well as the challenges and perspectives of each stage to be faced in the Northeast Region of Brazil.(AU)

Uso da bromelina na qualidade do sêmen caprino congelado/descongelado / Use of bromelain in the quality of frozen/thawed goat sêmen

The objective of this study was to evaluate the effect of bromelain on sperm quality, after defrosting, in goats. For this purpose, five Anglo Nubian goats were used. Semen collection was performed with the aid of an artificial vagina. The semen was evaluated for its macroscopic and microscopic parameters. After the analysis, the total volume of the pool was divided into three groups. One belonging to the control group (ACP-101/102®) and two treatment groups with ACP-101/102® enriched with bromelain in concentrations of 5% and 10%. The samples were cryopreserved with the aid of the Tk3000 device. Then, the straws were immersed in liquid nitrogen and stored in cryogenic cylinders. After one week the samples were thawed and evaluated by the system CASA (Computer Assisted Sperm Analysis). After thawing, the total sperm motility assessed by the system CASA was preserved in the control group and in the treatment group at a concentration of 5%. The curvilinear speed (LCV) and mean trajectory speed (VAP) of sperm were higher in the control group compared to the others. Thus, it is concluded that bromelain does not present genotoxicity to goat sperm, as well as its use is satisfactory in terms of the quality of seminal parameters after thawing.

Produção in vivo de embriões caprinos e ovinos submetidos ao meio de manutenção ACP® / In vivo production of goat and sheep embryos submitted to the ACP® maintenance médium

The use of ACP® as a means of maintenance in the stages of multiple ovulation and embryo transfer, has not yet been reported in the literature, although ACP® is a plant fluid rich in nutrients. Thus, the objective was to compare the efficiency of ACP® as a substitute for embryo maintenance medium during MOTE biotechnology in goats and sheep. For this, three donor goats, Anglo-Nubian breed and three donor sheep, Dorper breed were used. Fifteen recipient females of each species were used. The donors were submitted to the superovulation protocol and inseminated, and later the embryos were collected. After harvesting, the embryos were submitted to the control maintenance medium, TQC Holding® or ACP® maintenance medium. The recipients were synchronized simultaneously with the donors, and after 30 days the pregnancy diagnosis was made. It was obtained 10% of pregnant in goats and 75% of pregnant in sheep, whose embryos were submitted to the ACP® maintenance medium before the innovation. It is concluded that the means of maintenance of ACP® embryos did not negatively influence the embryonic quality and the development of pregnancy in small ruminants.

Avaliação estrutural de espermatozoide caprino criopreservado, através da microscopia eletrônica de transmissão / Ultrastructural evaluation of cryopreserved caprine sperm through transmission electronic microscopy

The ultrastructure evaluation allows the analysis of the sperm cell in a subcellular proportion that is not observed in optical microscopy. Transmission electron microscopy (MET) is a tool used to determine the size and shape of inorganic and biological structures based on the interaction of electrons incident on matter. In this sense, with the use of MET, the objective was to evaluate the ultrastructural changes after the semen manipulation, mainly in the freeze-thaw process, which were not observed in tests using optical microscopy, that is, the morphological integrity of the membranes and goat sperm organelles. The evaluation took place at the Institute of Biosciences of the University of Brasília (UnB). The semen straws were thawed and washed in PBS. Then, they were centrifuged and fixed, contrasted in bloc and subjected to dehydration. The samples were placed for polymerization and ultrathin cuts were made and stored until the time of MET evaluation. In the ultrastructural analyzes by MET in the present work, no harmful actions occurred in either the control or experimental groups. The head regions (plasma membrane and acrosome) remained preserved, with no change in DNA. In conclusion, MET is especially useful tool for cell evaluation.

Técnica do cometa para avaliação da integridade do DNA de espermatozoides caprinos criopreservados em ACP-101/102® / Comet technique to assess the DNA integrity of cryopreserved goat sperm in ACP-101/102®

Animal reproduction represents one of the most important factors, and the use of reproductive biotechnologies that help increase production is essential. The comet technique is the simple and quick way to detect pre-mutagenic lesions and assist in studies on environmental biomonitoring, toxicological genetics, biological radiation, DNA repair process and genetic ecotoxicology. The objective of this study was to evaluate the viability of DNA from sperm cells from goat semen submitted to the cryopreservation process in powdered coconut water (ACP101c/102c). The experiment was carried out at the Federal University of Piauí with two goats of reproductive age. The evaluation of the spermatic DNA integrity was performed using an immunofluorescence microscope. Classes from 0 to 3 were used, 0 being no damage and 3, the tail of the comet greater than twice the size of the nucleoid. The results obtained in the G2 test group (ACP 101c-102c) showed a slight tail formation, indicating a slight fragmentation of DNA. It was concluded that in the control group GC1 (TRIS + egg yolk of Gallu gallus domesticus) and experimental group (ACP 101c - 102c) there was no significant difference.

Técnica do cometa para avaliação da integridade do DNA de espermatozoides caprinos criopreservados em ACP-101/102® / Comet technique to assess the DNA integrity of cryopreserved goat sperm in ACP-101/102®

Animal reproduction represents one of the most important factors, and the use of reproductive biotechnologies that help increase production is essential. The comet technique is the simple and quick way to detect pre-mutagenic lesions and assist in studies on environmental biomonitoring, toxicological genetics, biological radiation, DNA repair process and genetic ecotoxicology. The objective of this study was to evaluate the viability of DNA from sperm cells from goat semen submitted to the cryopreservation process in powdered coconut water (ACP101c/102c). The experiment was carried out at the Federal University of Piauí with two goats of reproductive age. The evaluation of the spermatic DNA integrity was performed using an immunofluorescence microscope. Classes from 0 to 3 were used, 0 being no damage and 3, the tail of the comet greater than twice the size of the nucleoid. The results obtained in the G2 test group (ACP 101c-102c) showed a slight tail formation, indicating a slight fragmentation of DNA. It was concluded that in the control group GC1 (TRIS + egg yolk of Gallu gallus domesticus) and experimental group (ACP 101c - 102c) there was no significant difference.(AU)

Avaliação estrutural de espermatozoide caprino criopreservado, através da microscopia eletrônica de transmissão / Ultrastructural evaluation of cryopreserved caprine sperm through transmission electronic microscopy

The ultrastructure evaluation allows the analysis of the sperm cell in a subcellular proportion that is not observed in optical microscopy. Transmission electron microscopy (MET) is a tool used to determine the size and shape of inorganic and biological structures based on the interaction of electrons incident on matter. In this sense, with the use of MET, the objective was to evaluate the ultrastructural changes after the semen manipulation, mainly in the freeze-thaw process, which were not observed in tests using optical microscopy, that is, the morphological integrity of the membranes and goat sperm organelles. The evaluation took place at the Institute of Biosciences of the University of Brasília (UnB). The semen straws were thawed and washed in PBS. Then, they were centrifuged and fixed, contrasted in bloc and subjected to dehydration. The samples were placed for polymerization and ultrathin cuts were made and stored until the time of MET evaluation. In the ultrastructural analyzes by MET in the present work, no harmful actions occurred in either the control or experimental groups. The head regions (plasma membrane and acrosome) remained preserved, with no change in DNA. In conclusion, MET is especially useful tool for cell evaluation.(AU)

Uso da bromelina na qualidade do sêmen caprino congelado/descongelado / Use of bromelain in the quality of frozen/thawed goat sêmen

The objective of this study was to evaluate the effect of bromelain on sperm quality, after defrosting, in goats. For this purpose, five Anglo Nubian goats were used. Semen collection was performed with the aid of an artificial vagina. The semen was evaluated for its macroscopic and microscopic parameters. After the analysis, the total volume of the pool was divided into three groups. One belonging to the control group (ACP-101/102®) and two treatment groups with ACP-101/102® enriched with bromelain in concentrations of 5% and 10%. The samples were cryopreserved with the aid of the Tk3000 device. Then, the straws were immersed in liquid nitrogen and stored in cryogenic cylinders. After one week the samples were thawed and evaluated by the system CASA (Computer Assisted Sperm Analysis). After thawing, the total sperm motility assessed by the system CASA was preserved in the control group and in the treatment group at a concentration of 5%. The curvilinear speed (LCV) and mean trajectory speed (VAP) of sperm were higher in the control group compared to the others. Thus, it is concluded that bromelain does not present genotoxicity to goat sperm, as well as its use is satisfactory in terms of the quality of seminal parameters after thawing.(AU)

Produção in vivo de embriões caprinos e ovinos submetidos ao meio de manutenção ACP® / In vivo production of goat and sheep embryos submitted to the ACP® maintenance médium

The use of ACP® as a means of maintenance in the stages of multiple ovulation and embryo transfer, has not yet been reported in the literature, although ACP® is a plant fluid rich in nutrients. Thus, the objective was to compare the efficiency of ACP® as a substitute for embryo maintenance medium during MOTE biotechnology in goats and sheep. For this, three donor goats, Anglo-Nubian breed and three donor sheep, Dorper breed were used. Fifteen recipient females of each species were used. The donors were submitted to the superovulation protocol and inseminated, and later the embryos were collected. After harvesting, the embryos were submitted to the control maintenance medium, TQC Holding® or ACP® maintenance medium. The recipients were synchronized simultaneously with the donors, and after 30 days the pregnancy diagnosis was made. It was obtained 10% of pregnant in goats and 75% of pregnant in sheep, whose embryos were submitted to the ACP® maintenance medium before the innovation. It is concluded that the means of maintenance of ACP® embryos did not negatively influence the embryonic quality and the development of pregnancy in small ruminants.(AU)

Diluente Tris suplementado com óleo de Mauritia flexuoxa sobre a qualidade do sêmen caprino após a criopreservação / Tris diluent supplemented with Mauritia flexuoxa oil on the quality of goat semen after cryopreservation

Objetivou-se verificar os efeitos, nos parâmetros espermáticos, na integridade mitocondrial, acrossomal e de membrana em células espermáticas, desencadeados pelo uso do Tris (Tris hidroximetil aminometano) suplementado com óleo de Mauritia flexuoxacomo diluente para criopreservação de sêmen caprino. Quatro caprinos clinicamente saudáveis foram utilizados. Os animais eram alimentados diariamente com volumoso (Pennisetum purpureum, Schum.), concentrado (ração peletizada com teor de 20% proteína, 300 g/animal/dia) e sal mineral específico para Caprinos (Caprinofós®), à vontade. Dois ensaios foram realizados: I ­ Teste de toxicidade; II ­ Criopreservação do sêmen com concentrações ideais. No teste de toxicidade as concentrações avaliadas foram: 5%, 10%, 15% e 20% de diluente a base de óleo de Mauritia flexuoxa. Após o teste de toxicidade, foi escolhido a concentraçãoque apresentou o melhor resultado (5%). Logo após, foram realizadas mais 32 coletas, que foram diluídas em Tris-gema-glicerol (grupo controle) ou diluente contendo óleo vegetal (Mauritia flexuoxa). As amostras foram criopreservadas com auxílio do aparelho Tk3000®. Após o período mínimo de uma semana as palhetas foram descongeladas em banho-maria a 37 °C por 30 segundos, acondicionadas em microtubos de centrifugação e homogeneizadas para a análise imediata de motilidade, vigor espermático e morfologia. Em seguida, por meio de sondas fluorescentes foram avaliadas a integridade de acrossomo, membrana plasmática (Diacetato de Carboxifluresceína e Iodeto de Propídeo) e função mitocondrial sob microscopia de epifluorescência. Quanto a motilidade e vigor, integridade mitocondrial e acrossomal, o grupo buriti foi inferior ao grupo controle. O Tris suplementado com óleo de Mauritia flexuoxa na concentração de 5% não influenciou significativamente a qualidade espermática, porém, observou-se morfologia e integridade de membrana favoráveis. Dessa forma, sendo uma alternativa para substituição de diluentes a base de produtos de origem animal.

The objective was to verify the effects, sperm parameters, mitochondrial, acrosomal and membrane integrity in sperm cells, triggered by the use of Tris (Tris hydroxymethyl aminomethane) supplemented with Mauritia flexuoxa oil as a diluent for cryopreservation of goat semen. Four goats clinically healthy were used. The animals were fed daily with bulky (Pennisetum purpureum, Schum.), concentrate (pelleted feed with 20% protein content, 300 g / animal / day) and mineral salt Specific for Goats (Caprinofós®), ad libitum. Two tests were carried out: I - Toxicity test; II - Semen cryopreservation with ideal concentrations. In the toxicity test as selected were: 5%, 10%, 15% and 20% of Mauritia flexuoxa oil-based diluent. After the toxicity test, the concentration that showed the best result (5%) was chosen. Soon after, a further 32 samples were obtained, which were diluted in Tris-glycerol (control group) or diluent containing vegetable oil (Mauritia flexuoxa). The samples were cryopreserved using the Tk3000® machine. After a minimum of one week, the samples were thawed in a 37 ° C water bath for 30 seconds, packed in centrifugation microtubes and homogenized for immediate analysis of motility, sperm vigor and morphology. Then, by means of fluorescent probes, the integrity of the acrosome, plasma membrane (Carboxyflurescein diacetate and Propidium Iodide) and mitochondrial function under epifluorescence microscopy were evaluated. As for motility and vigor, mitochondrial and acrosomal integrity, the buriti group was inferior to the control group. Tris supplemented with Mauritia flexuoxa oil at a concentration of 5% did not significantly influence sperm quality, however, favorable motility, morphology and membrane integrity were observed. Thus, being an alternative to replace diluents based on products of animal origin.

Diluente Tris suplementado com óleo de Mauritia flexuoxa sobre a qualidade do sêmen caprino após a criopreservação / Tris diluent supplemented with Mauritia flexuoxa oil on the quality of goat semen after cryopreservation

Objetivou-se verificar os efeitos, nos parâmetros espermáticos, na integridade mitocondrial, acrossomal e de membrana em células espermáticas, desencadeados pelo uso do Tris (Tris hidroximetil aminometano) suplementado com óleo de Mauritia flexuoxa como diluente para criopreservação de sêmen caprino. Quatro caprinos clinicamente saudáveis foram utilizados. Os animais eram alimentados diariamente com volumoso (Pennisetum purpureum, Schum.), concentrado (ração peletizada com teor de 20% proteína, 300 g/animal/dia) e sal mineral específico para Caprinos (Caprinofós®), à vontade. Dois ensaios foram realizados: I Teste de toxicidade; II Criopreservação do sêmen com concentrações ideais. No teste de toxicidade as concentrações avaliadas foram: 5%, 10%, 15% e 20% de diluente a base de óleo de Mauritia flexuoxa. Após o teste de toxicidade, foi escolhido a concentração que apresentou o melhor resultado (5%). Logo após, foram realizadas mais 32 coletas, que foram diluídas em Tris-gema-glicerol (grupo controle) ou diluente contendo óleo vegetal (Mauritia flexuoxa). As amostras foram criopreservadas com auxílio do aparelho Tk3000®. Após o período mínimo de uma semana as palhetas foram descongeladas em banho-maria a 37 °C por 30 segundos, acondicionadas em microtubos de centrifugação e homogeneizadas para a análise imediata de motilidade, vigor espermático e morfologia. Em seguida, por meio de sondas fluorescentes foram avaliadas a integridade de acrossomo, membrana plasmática (Diacetato de Carboxifluresceína e Iodeto de Propídeo) e função mitocondrial sob microscopia de epifluorescência. Quanto a motilidade e vigor, integridade mitocondrial e acrossomal, o grupo buriti foi inferior ao grupo controle. O Tris suplementado com óleo de Mauritia flexuoxa na concentração de 5% não influenciou significativamente a qualidade espermática, porém, observouse morfologia e integridade de membrana favoráveis. Dessa forma, sendo uma alternativa para substituição de diluentes a base de produtos de origem animal.(AU)

The objective was to verify the effects, sperm parameters, mitochondrial, acrosomal and membrane integrity in sperm cells, triggered by the use of Tris (Tris hydroxymethyl aminomethane) supplemented with Mauritia flexuoxa oil as a diluent for cryopreservation of goat semen. Four goats clinically healthy were used. The animals were fed daily with bulky (Pennisetum purpureum, Schum.), concentrate (pelleted feed with 20% protein content, 300 g / animal / day) and mineral salt Specific for Goats (Caprinofós®), ad libitum. Two tests were carried out: I - Toxicity test; II - Semen cryopreservation with ideal concentrations. In the toxicity test as selected were: 5%, 10%, 15% and 20% of Mauritia flexuoxa oil-based diluent. After the toxicity test, the concentration that showed the best result (5%) was chosen. Soon after, a further 32 samples were obtained, which were diluted in Tris-glycerol (control group) or diluent containing vegetable oil (Mauritia flexuoxa). The samples were cryopreserved using the Tk3000® machine. After a minimum of one week, the samples were thawed in a 37 ° C water bath for 30 seconds, packed in centrifugation microtubes and homogenized for immediate analysis of motility, sperm vigor and morphology. Then, by means of fluorescent probes, the integrity of the acrosome, plasma membrane (Carboxyflurescein diacetate and Propidium Iodide) and mitochondrial function under epifluorescence microscopy were evaluated. As for motility and vigor, mitochondrial and acrosomal integrity, the buriti group was inferior to the control group. Tris supplemented with Mauritia flexuoxa oil at a concentration of 5% did not significantly influence sperm quality, however, favorable motility, morphology and membrane integrity were observed. Thus, being an alternative to replace diluents based on products of animal origin.(AU)

Diluente Tris suplementado com óleo de Mauritia flexuoxa sobre a qualidade do sêmen caprino após a criopreservação / Tris diluent supplemented with Mauritia flexuoxa oil on the quality of goat semen after cryopreservation

Objetivou-se verificar os efeitos, nos parâmetros espermáticos, na integridade mitocondrial, acrossomal e de membrana em células espermáticas, desencadeados pelo uso do Tris (Tris hidroximetil aminometano) suplementado com óleo de Mauritia flexuoxa como diluente para criopreservação de sêmen caprino. Quatro caprinos clinicamente saudáveis foram utilizados. Os animais eram alimentados diariamente com volumoso (Pennisetum purpureum, Schum.), concentrado (ração peletizada com teor de 20% proteína, 300 g/animal/dia) e sal mineral específico para Caprinos (Caprinofós®), à vontade. Dois ensaios foram realizados: I – Teste de toxicidade; II – Criopreservação do sêmen com concentrações ideais. No teste de toxicidade as concentrações avaliadas foram: 5%, 10%, 15% e 20% de diluente a base de óleo de Mauritia flexuoxa. Após o teste de toxicidade, foi escolhido a concentração que apresentou o melhor resultado (5%). Logo após, foram realizadas mais 32 coletas, que foram diluídas em Tris-gema-glicerol (grupo controle) ou diluente contendo óleo vegetal (Mauritia flexuoxa). As amostras foram criopreservadas com auxílio do aparelho Tk3000®. Após o período mínimo de uma semana as palhetas foram descongeladas em banho-maria a 37 °C por 30 segundos, acondicionadas em microtubos de centrifugação e homogeneizadas para a análise imediata de motilidade, vigor espermático e morfologia. Em seguida, por meio de sondas fluorescentes foram avaliadas a integridade de acrossomo, membrana plasmática (Diacetato de Carboxifluresceína e Iodeto de Propídeo) e função mitocondrial sob microscopia de epifluorescência. Quanto a motilidade e vigor, integridade mitocondrial e acrossomal, o grupo buriti foi inferior ao grupo controle. O Tris suplementado com óleo de Mauritia flexuoxa na concentração de 5% não influenciou significativamente a qualidade espermática, porém, observouse morfologia e integridade de membrana favoráveis. Dessa forma, sendo uma alternativa para substituição de diluentes a base de produtos de origem animal.

The objective was to verify the effects, sperm parameters, mitochondrial, acrosomal and membrane integrity in sperm cells, triggered by the use of Tris (Tris hydroxymethyl aminomethane) supplemented with Mauritia flexuoxa oil as a diluent for cryopreservation of goat semen. Four goats clinically healthy were used. The animals were fed daily with bulky (Pennisetum purpureum, Schum.), concentrate (pelleted feed with 20% protein content, 300 g / animal / day) and mineral salt Specific for Goats (Caprinofós®), ad libitum. Two tests were carried out: I - Toxicity test; II - Semen cryopreservation with ideal concentrations. In the toxicity test as selected were: 5%, 10%, 15% and 20% of Mauritia flexuoxa oil-based diluent. After the toxicity test, the concentration that showed the best result (5%) was chosen. Soon after, a further 32 samples were obtained, which were diluted in Tris-glycerol (control group) or diluent containing vegetable oil (Mauritia flexuoxa). The samples were cryopreserved using the Tk3000® machine. After a minimum of one week, the samples were thawed in a 37 ° C water bath for 30 seconds, packed in centrifugation microtubes and homogenized for immediate analysis of motility, sperm vigor and morphology. Then, by means of fluorescent probes, the integrity of the acrosome, plasma membrane (Carboxyflurescein diacetate and Propidium Iodide) and mitochondrial function under epifluorescence microscopy were evaluated. As for motility and vigor, mitochondrial and acrosomal integrity, the buriti group was inferior to the control group. Tris supplemented with Mauritia flexuoxa oil at a concentration of 5% did not significantly influence sperm quality, however, favorable motility, morphology and membrane integrity were observed. Thus, being an alternative to replace diluents based on products of animal origin.

Uso da polpa desidratada do fruto de Mauritia flexuosa como suplemento ao diluente de congelação do sêmen caprino / Use of dehydrated pulp of Mauritia flexuosa fruit as supplement to freezing extender of goat semen

Objetivou-se avaliar a qualidade in vitro do sêmen caprino descongelado utilizando diluentesuplementado com a polpa desidratada do fruto de Mauritia flexuosa. O experimento foi dividido emduas etapas. Na primeira, foram utilizados 15 pools,fracionados em 13 tratamentos com diferentesconcentrações do extrato bruto. Os melhores resultados de viabilidade espermática obtidos na primeiraetapa foram utilizadas na segunda etapa (criopreservação). Para isto, foram formados dois gruposutilizando 15 pools, sendo um diluente constituído (TRIS + 7% glicerol + melhores concentrações doextrato bruto) e outro pelo diluente (TRIS + 2,5% gema de ovo + 7% glicerol + melhores concentraçõesdo extrato bruto). Na primeira etapa os grupos contendo baixa quantidade do extrato não diferiram dogrupo controle (P≤0,05). Todavia na segunda etapa, após descongelação, os grupos TRIS contendo 2,5%ou 0% de gema de ovo apresentaram diferença significativa, onde o grupo TB06GLGE foi superior aogrupo controle. Portanto, a polpa desidratada do fruto de Mauritia flexuosa,nas concentrações de 0,25% a1%, não atuou de forma benéfica sobre parâmetros espermáticos do sêmen caprino após acriopreservação/descongelação.(AU)

The objective was to evaluate the in vitro quality of the thawed goat semen using diluentsupplemented with the dehydrated pulp of the Mauritia flexuosa fruit. The experiment was divided intotwo stages. In the first, 15 fractionated pools were used in 13 treatments with different concentrations ofthe crude extract. The best results of sperm viability obtained in the first experimental stage were used inthe second experimental stage (cryopreservation). Afterwards, two groups were formed using 15 pools,one constituent (TRIS + 7% glycerol + best concentrations of the crude extract) and another by thediluent (TRIS + 2,5% egg yolk + 7% glycerol + best concentrations of the crude extract). In the firststage, the groups containing low amount of extract did not differ from the control group (P≤0.05).However, in the second stage, after thawing, TRIS groups containing 2.5% or 0% egg yolk presented asignificant difference, where the TB06GLGE group was superior to the control group. Therefore, thedehydrated fruit pulp of Mauritia flexuosa at concentrations of 0.25% to 1% did not benefit goat semenparameters after cryopreservation/thawing.(AU)

Uso da polpa desidratada do fruto de Mauritia flexuosa como suplemento ao diluente de congelação do sêmen caprino / Use of dehydrated pulp of Mauritia flexuosa fruit as supplement to freezing extender of goat semen

Objetivou-se avaliar a qualidade in vitro do sêmen caprino descongelado utilizando diluentesuplementado com a polpa desidratada do fruto de Mauritia flexuosa. O experimento foi dividido emduas etapas. Na primeira, foram utilizados 15 pools,fracionados em 13 tratamentos com diferentesconcentrações do extrato bruto. Os melhores resultados de viabilidade espermática obtidos na primeiraetapa foram utilizadas na segunda etapa (criopreservação). Para isto, foram formados dois gruposutilizando 15 pools, sendo um diluente constituído (TRIS + 7% glicerol + melhores concentrações doextrato bruto) e outro pelo diluente (TRIS + 2,5% gema de ovo + 7% glicerol + melhores concentraçõesdo extrato bruto). Na primeira etapa os grupos contendo baixa quantidade do extrato não diferiram dogrupo controle (P≤0,05). Todavia na segunda etapa, após descongelação, os grupos TRIS contendo 2,5%ou 0% de gema de ovo apresentaram diferença significativa, onde o grupo TB06GLGE foi superior aogrupo controle. Portanto, a polpa desidratada do fruto de Mauritia flexuosa,nas concentrações de 0,25% a1%, não atuou de forma benéfica sobre parâmetros espermáticos do sêmen caprino após acriopreservação/descongelação.

The objective was to evaluate the in vitro quality of the thawed goat semen using diluentsupplemented with the dehydrated pulp of the Mauritia flexuosa fruit. The experiment was divided intotwo stages. In the first, 15 fractionated pools were used in 13 treatments with different concentrations ofthe crude extract. The best results of sperm viability obtained in the first experimental stage were used inthe second experimental stage (cryopreservation). Afterwards, two groups were formed using 15 pools,one constituent (TRIS + 7% glycerol + best concentrations of the crude extract) and another by thediluent (TRIS + 2,5% egg yolk + 7% glycerol + best concentrations of the crude extract). In the firststage, the groups containing low amount of extract did not differ from the control group (P≤0.05).However, in the second stage, after thawing, TRIS groups containing 2.5% or 0% egg yolk presented asignificant difference, where the TB06GLGE group was superior to the control group. Therefore, thedehydrated fruit pulp of Mauritia flexuosa at concentrations of 0.25% to 1% did not benefit goat semenparameters after cryopreservation/thawing.

Maturação in vitro de oócitos ovinos submetidos à congelação lenta / In vitro maturation of cryopreserved ovine oocytes subjected to slow freezing

A maturação in vitro de oócitos submetidos ao processo de criopreservação, ainda compreende um desafio para o sucesso da reprodução assistida na medicina veterinária. Devido a isso, estudos são desenvolvidos a fim de identificar, amenizar e superar as limitações encontradas. Nesse sentido, objetivou-se realizar a avaliação da maturação in vitro de oócitos ovinos após criopreservação pelo método de congelação lenta. Para tanto, foram colhidos 204 ovários oriundos de 102 ovelhas púberes (SPRD) pertencentes a abatedouros localizados no município de Teresina, Piauí. Os ovários foram transportados para o laboratório e, posteriormente, foram aspirados por meio de um aspirador cirúrgicoadaptado. Um total de 180 oócitos foram desnudados e, então, submetidos à congelação lenta em sistema automatizado (TK 3000®). Posteriormente foram descongelados, e submetidos à maturação in vitro(MIV). Em seguida, procedeu-se a avaliação da maturação nuclear. Os resultados foram avaliados por meio do teste de Qui-quadrado de Pearson (P ≤ 0,05). Após descongelação, 22,8% dos oócitos na avaliação em estereomicroscópio (45x) apresentavam lesões de zona pelúcida e de oolema. Dos 139 oócitos submetidos a MIV, oito maturaram (5,75%). Conclui-se que a congelação lenta de oócitos ovinos pode influenciar a maturação in vitro, devido a lesões de membrana plasmática e zona pelúcida.(AU)

The in vitro maturation of oocytes submitted to the cryopreservation process, still comprises a challenge for the success of assisted reproduction in veterinary medicine. Due to this, studies are developed in order to identify, ameliorate and overcome the limitations found. The objective of this study was to evaluate the in vitro maturation of ovine oocytes after cryopreservation by the slow freezing method. For that, 204 ovaries from 102 pubertal sheep (SPRD) belonging to slaughterhouses located in the city of Teresina, Piauí, were collected. The ovaries were transported to the laboratory and subsequently aspirated by means of an adapted surgical aspirator. A total of 180 CCO's were obtained, which were stripped and then subjected to slow freezing in an automated system (TK 3000®). Later they were thawed and submitted to in vitro maturation (IVM). Next, the nuclear maturation was evaluated. Results were evaluated using Pearson's chi-square test (P ≤ 0.05). After thawing, 22.8% of the oocytes in the stereomicroscope (45x) evaluation presented lesions of the zona pellucida and oolema. Of the 139 oocytes submitted to IVM, eight maturated (5.75%). It is concluded that slow freezing of sheep oocytesmay influence in vitro maturation due to plasma membrane and zona pellucida lesions.(AU)

Maturação in vitro de oócitos ovinos submetidos à congelação lenta / In vitro maturation of cryopreserved ovine oocytes subjected to slow freezing

A maturação in vitro de oócitos submetidos ao processo de criopreservação, ainda compreende um desafio para o sucesso da reprodução assistida na medicina veterinária. Devido a isso, estudos são desenvolvidos a fim de identificar, amenizar e superar as limitações encontradas. Nesse sentido, objetivou-se realizar a avaliação da maturação in vitro de oócitos ovinos após criopreservação pelo método de congelação lenta. Para tanto, foram colhidos 204 ovários oriundos de 102 ovelhas púberes (SPRD) pertencentes a abatedouros localizados no município de Teresina, Piauí. Os ovários foram transportados para o laboratório e, posteriormente, foram aspirados por meio de um aspirador cirúrgicoadaptado. Um total de 180 oócitos foram desnudados e, então, submetidos à congelação lenta em sistema automatizado (TK 3000®). Posteriormente foram descongelados, e submetidos à maturação in vitro(MIV). Em seguida, procedeu-se a avaliação da maturação nuclear. Os resultados foram avaliados por meio do teste de Qui-quadrado de Pearson (P ≤ 0,05). Após descongelação, 22,8% dos oócitos na avaliação em estereomicroscópio (45x) apresentavam lesões de zona pelúcida e de oolema. Dos 139 oócitos submetidos a MIV, oito maturaram (5,75%). Conclui-se que a congelação lenta de oócitos ovinos pode influenciar a maturação in vitro, devido a lesões de membrana plasmática e zona pelúcida.

The in vitro maturation of oocytes submitted to the cryopreservation process, still comprises a challenge for the success of assisted reproduction in veterinary medicine. Due to this, studies are developed in order to identify, ameliorate and overcome the limitations found. The objective of this study was to evaluate the in vitro maturation of ovine oocytes after cryopreservation by the slow freezing method. For that, 204 ovaries from 102 pubertal sheep (SPRD) belonging to slaughterhouses located in the city of Teresina, Piauí, were collected. The ovaries were transported to the laboratory and subsequently aspirated by means of an adapted surgical aspirator. A total of 180 CCO's were obtained, which were stripped and then subjected to slow freezing in an automated system (TK 3000®). Later they were thawed and submitted to in vitro maturation (IVM). Next, the nuclear maturation was evaluated. Results were evaluated using Pearson's chi-square test (P ≤ 0.05). After thawing, 22.8% of the oocytes in the stereomicroscope (45x) evaluation presented lesions of the zona pellucida and oolema. Of the 139 oocytes submitted to IVM, eight maturated (5.75%). It is concluded that slow freezing of sheep oocytesmay influence in vitro maturation due to plasma membrane and zona pellucida lesions.

Programas de inseminação artificial com sêmen congelado de caprinos e ovinos por laparoscopia no Nordeste do Brasil / Programs of artificial insemination with frozen semen of goats and sheep by laparoscopy in Northeast of Brazil

Dentre as biotécnicas aplicadas a reprodução animal, a inseminação artificial (IA) consiste na aplicação do sêmen no aparelho reprodutor da fêmea por meio instrumental. A IA oferece vários benefícios aos criadores, como aceleração do melhoramento genético de animais de interesse econômico, maior controle de doenças sexualmente transmissíveis, facilita a realização do teste de progênie, viabiliza a utilização de sêmen congelado de reprodutores alojados em outras localidades e possibilita que machos com subfertilidade adquirida produzam descendentes. Suas limitações estão relacionadas com carência de mão de obra qualificada, principalmente quando se utiliza a inseminação artificial por laparoscopia, infraestrutura mínima na propriedade para a realização dos procedimentos e aumento dos custos com a aquisição de hormônios. Nesse contexto, a presente revisão de literatura relata os principais pontos que devem ser considerados a fim de superar algumas limitações, bem como, as vantagens da utilização e escolha da melhor técnica.(AU)

Artificial insemination (AI) through laparoscopic techniques has been an important alternative to minimize the difficulties observed in cervical AI in small ruminants. Artificial insemination by laparoscopy facilitates the deposition of the semen directly into the uterine horns of the female, and does not present the cervix as a barrier, especially in sheep that have high sinuosity of the cervical rings. Thus, the use of frozen semen with laparoscopic intrauterine deposition has been important to obtain better fertility indexes in goats and sheep. AI offers several benefits to breeders, such as accelerating the genetic improvement of animals of economic interest, greater control of sexually transmitted diseases, facilitating progeny testing, enabling the use of frozen semen from breeding animals housed in other locations and enabling males with acquired subfertility produce descendants.(AU)

Programas de inseminação artificial com sêmen congelado de caprinos e ovinos por laparoscopia no Nordeste do Brasil / Programs of artificial insemination with frozen semen of goats and sheep by laparoscopy in Northeast of Brazil

Dentre as biotécnicas aplicadas a reprodução animal, a inseminação artificial (IA) consiste na aplicação do sêmen no aparelho reprodutor da fêmea por meio instrumental. A IA oferece vários benefícios aos criadores, como aceleração do melhoramento genético de animais de interesse econômico, maior controle de doenças sexualmente transmissíveis, facilita a realização do teste de progênie, viabiliza a utilização de sêmen congelado de reprodutores alojados em outras localidades e possibilita que machos com subfertilidade adquirida produzam descendentes. Suas limitações estão relacionadas com carência de mão de obra qualificada, principalmente quando se utiliza a inseminação artificial por laparoscopia, infraestrutura mínima na propriedade para a realização dos procedimentos e aumento dos custos com a aquisição de hormônios. Nesse contexto, a presente revisão de literatura relata os principais pontos que devem ser considerados a fim de superar algumas limitações, bem como, as vantagens da utilização e escolha da melhor técnica.

Artificial insemination (AI) through laparoscopic techniques has been an important alternative to minimize the difficulties observed in cervical AI in small ruminants. Artificial insemination by laparoscopy facilitates the deposition of the semen directly into the uterine horns of the female, and does not present the cervix as a barrier, especially in sheep that have high sinuosity of the cervical rings. Thus, the use of frozen semen with laparoscopic intrauterine deposition has been important to obtain better fertility indexes in goats and sheep. AI offers several benefits to breeders, such as accelerating the genetic improvement of animals of economic interest, greater control of sexually transmitted diseases, facilitating progeny testing, enabling the use of frozen semen from breeding animals housed in other locations and enabling males with acquired subfertility produce descendants.