Made available in DSpace on 2014-06-11T19:29:17Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-02-22Bitstream added on 2014-06-13T18:48:33Z : No. of bitstreams: 1 monteiro_ga_me_botfmvz.pdf: 8347367 bytes, checksum: 82c2cef3b1dcf4f8284dbffecca4034d (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / A recuperação de espermatozóides da cauda do epidídimo e sua criopreservação pode ser a última chance para recuperação do material genético quando ocorre morte súbita ou lesão grave em garanhões de alto valor genético. Sendo assim, o objetivo do experimento I foi comparar os parâmetros espermáticos dos espermatozóides da cauda do epidídimo recuperados imediatamente após orquiectomia e em diferentes momentos após armazenamento a 5°C e a temperatura ambiente. Já o experimento II, teve o objetivo de comparar os parâmetros espermáticos e fertilidade dos espermatozóides do ejaculado e do epidídimo recuperados logo depois da orquiectomia e após armazenamento por 24 horas a 5°C. No experimento I, 48 garanhões foram submetidos à orquiectomia bilateral, sendo que em oito a colheita dos espermatozóides do epidídimo foi realizada imediatamente após orquiectomia (grupo controle). Nos outros 40 garanhões, um epidídimo foi armazenado a temperatura ambiente e o contralateral armazenado a 5°C por 6, 12, 18, 24 e 30 horas, de acordo com o grupo. No experimento II, dois ejaculados de oito garanhões foram colhidos com vagina artificial e congelados (grupo EJ-0h). Uma semana após, os garanhões foram submetidos à orquiectomia bilateral, sendo que os espermatozóides de um epidídimo foram congelados imediatamente após orquiectomia (grupo EP-0h) e o epidídimo contralateral foi previamente armazenado por 24 horas a 5°C (EP-24h). O teste de fertilidade demonstrou que o grupo EP-0h (92,3%; n=13) tendem a ser maior que os grupos EJ-0h (61,5%; n=13) e EP-24h (61,5%; n=13). Conclui-se que o armazenamento dos testículos-epidídimos a 5°C proporcionou melhor preservação espermática e que, independente da temperatura, a motilidade progressiva é o parâmetro espermático mais sensível ao tempo de armazenamento. / Cauda epididymis sperm recovery and cryopreservation may be the last chance to obtain genetical material when sudden death or serious injury occur in valuable stallions. Thus, the aim of experiment I was to compare sperm parameters of epididymal sperm recovered immediately after orchiectomy and at different moments after storage at 5°C and at room temperature. Experiment II aimed to compare sperm parameters and fertility of ejaculated sperm and epididymal sperm recovered immediately after orchiectomy and after storage for 24h at 5°C. In experiment I, 48 stallions were submitted to bilateral orchiectomy, in eight of those the sperm collection were done immediately after orchiectomy (control group). In the other 40 stallions, one epididymis was stored at room temperature and the other was stored at 5°C for 6, 12, 18, 24 and 30 hours accorded to groups. In experiment II, two ejaculated from eight stallions were obtained with artificial vagina and cryopreserved (group EJ-0h). One week later, the stallions were submitted to bilateral orchiectomy, and the sperm of one epididymal were frozen immediately after orchiectomy (group EP-0h) and the contralateral epididymal was previously storage for 24h at 5°C (EP-24h). Fertility test showed that group EP-0h (92,3%; n=13) tended to be higher than groups EJ-0h (61,5%; n=13) and EP-24h (61,5%; n=13). These results allowed concluding that storage of the testis-epididymis complex at 5°C is more efficient in preserving sperm parameters than room temperature storage and that progressive motility is the parameter that is more affected by storage period, regardless of the temperature.

Orientador: Frederico Ozanam Papa / Banca: Marco Antonio Alvarenga / Banca: Fabiana Ferreira de Souza / Resumo: A recuperação de espermatozóides da cauda do epidídimo e sua criopreservação pode ser a última chance para recuperação do material genético quando ocorre morte súbita ou lesão grave em garanhões de alto valor genético. Sendo assim, o objetivo do experimento I foi comparar os parâmetros espermáticos dos espermatozóides da cauda do epidídimo recuperados imediatamente após orquiectomia e em diferentes momentos após armazenamento a 5°C e a temperatura ambiente. Já o experimento II, teve o objetivo de comparar os parâmetros espermáticos e fertilidade dos espermatozóides do ejaculado e do epidídimo recuperados logo depois da orquiectomia e após armazenamento por 24 horas a 5°C. No experimento I, 48 garanhões foram submetidos à orquiectomia bilateral, sendo que em oito a colheita dos espermatozóides do epidídimo foi realizada imediatamente após orquiectomia (grupo controle). Nos outros 40 garanhões, um epidídimo foi armazenado a temperatura ambiente e o contralateral armazenado a 5°C por 6, 12, 18, 24 e 30 horas, de acordo com o grupo. No experimento II, dois ejaculados de oito garanhões foram colhidos com vagina artificial e congelados (grupo EJ-0h). Uma semana após, os garanhões foram submetidos à orquiectomia bilateral, sendo que os espermatozóides de um epidídimo foram congelados imediatamente após orquiectomia (grupo EP-0h) e o epidídimo contralateral foi previamente armazenado por 24 horas a 5°C (EP-24h). O teste de fertilidade demonstrou que o grupo EP-0h (92,3%; n=13) tendem a ser maior que os grupos EJ-0h (61,5%; n=13) e EP-24h (61,5%; n=13). Conclui-se que o armazenamento dos testículos-epidídimos a 5°C proporcionou melhor preservação espermática e que, independente da temperatura, a motilidade progressiva é o parâmetro espermático mais sensível ao tempo de armazenamento. / Abstract: Cauda epididymis sperm recovery and cryopreservation may be the last chance to obtain genetical material when sudden death or serious injury occur in valuable stallions. Thus, the aim of experiment I was to compare sperm parameters of epididymal sperm recovered immediately after orchiectomy and at different moments after storage at 5°C and at room temperature. Experiment II aimed to compare sperm parameters and fertility of ejaculated sperm and epididymal sperm recovered immediately after orchiectomy and after storage for 24h at 5°C. In experiment I, 48 stallions were submitted to bilateral orchiectomy, in eight of those the sperm collection were done immediately after orchiectomy (control group). In the other 40 stallions, one epididymis was stored at room temperature and the other was stored at 5°C for 6, 12, 18, 24 and 30 hours accorded to groups. In experiment II, two ejaculated from eight stallions were obtained with artificial vagina and cryopreserved (group EJ-0h). One week later, the stallions were submitted to bilateral orchiectomy, and the sperm of one epididymal were frozen immediately after orchiectomy (group EP-0h) and the contralateral epididymal was previously storage for 24h at 5°C (EP-24h). Fertility test showed that group EP-0h (92,3%; n=13) tended to be higher than groups EJ-0h (61,5%; n=13) and EP-24h (61,5%; n=13). These results allowed concluding that storage of the testis-epididymis complex at 5°C is more efficient in preserving sperm parameters than room temperature storage and that progressive motility is the parameter that is more affected by storage period, regardless of the temperature. / Mestre

[ES] En las últimas décadas, la anguila europea Anguilla anguila ha sufrido una disminución drástica de su población lo que ha llevado su inclusión como especie en peligro crítico en la lista roja UICN. Esta situación, junto con la gran importancia comercial de esta especie, evidencia la necesidad de tomar acciones como el desarrollo de la reproducción en cautividad y el control de la pesca. Una de las herramientas más interesantes para su uso en la biología de la conservación es la criopreservación de espermatozoides, que presenta varias ventajas para esta especie, incluyendo la sincronización de gametos, la selección de líneas genéticas o su uso para la creación de un criobanco. Sin embargo, el desarrollo de protocolos de criopreservación necesariamente requieren esperma de buena calidad. Además, se necesita un método preciso para evaluar la calidad del esperma tanto antes como después de la criopreservación. Sobre esta última cuestión, la motilidad de los espermatozoides de los peces se considera uno de los mejores biomarcadores para la evaluación de la calidad de los espermatozoides en los peces, y se puede estudiar de forma subjetiva u objetiva utilizando sistemas "computer assisted sperm analysis" (CASA-Mot). Primero, se realizó un experimento para evaluar la precisión y la exactitud de ambos métodos para estudiar la motilidad del esperma: el método subjetivo y la técnica objetiva que utiliza el sistema CASA-Mot. Además, se probó si el grado de experiencia de los técnicos en el caso del método subjetivo tiene un efecto en la precisión de la estimación de la motilidad y, por lo tanto, hay una influencia del personal del laboratorio en la evaluación de la motilidad del esperma. Aquí concluimos que tanto el método como la experiencia técnica eran factores clave para evaluar con precisión la motilidad del esperma en la anguila europea, por lo que se requiere el uso de CASA-Mot junto con material calificado para obtener resultados fehacientes. En segundo lugar, se evaluaron métodos alternativos para la maduración de los machos de anguila europeos probando dos tratamientos hormonales diferentes: OVI, una gonadotropina recombinante; y VET, una gonadotropina purificada a partir de orina femenina. Después de elegir el mejor tratamiento hormonal de los dos, se evaluó el efecto de tres dosis diferentes con el objetivo de obtener el mayor rendimiento al menor coste. Los resultados de este experimento apuntaron a OVI como el mejor tratamiento hormonal en una dosis semanal de 1.5 UI/g de pez, que proporciona la mayor rentabilidad, obteniendo esperma de alta calidad a menor precio. En un tercer experimento, y utilizando los conocimientos adquiridos en los dos primeros experimentos, se realizaron una serie de experimentos para estandarizar los protocolos de criopreservación de esperma de anguila europea disponibles en ese momento (utilizando DMSO o metanol como crioprotector). Los resultados apuntaron al protocolo que utiliza el metanol como el mejor de ellos dos en términos de motilidad, velocidad y viabilidad de los espermatozoides y la preservación de la integridad del ADN. Siguiendo este último método estandarizado, se realizó un cuarto experimento con el objetivo de mejorar el protocolo en términos de volumen (volúmenes de esperma más grandes) y de calidad espermática. Además, se desarrolló un protocolo simple de almacenamiento a corto plazo para complementar las opciones de preservar el esperma durante diferentes períodos de tiempo. De todas las condiciones de almacenamiento probadas, las diluciones 1/50 a 4 ºC mostraron los mejores resultados, manteniendo la motilidad en comparación con el control durante 3 días, y manteniendo cierta motilidad espermática (12%) después de 7 días. A partir del experimento de criopreservación, fue posible aumentar los volúmenes a 2 y 5 mL sin perder la calidad del esperma en comparación con volúmenes más pequeños, y mejorando las mot / [CAT] En les últimes dècades, l'anguila europea Anguilla anguila ha sofert una disminució dràstica de la seva població el que ha portat la seva inclusió com a espècie en perill crític en la llista vermella UICN. Aquesta situació, juntament amb la gran importància comercial d'aquesta espècie, evidencia la necessitat de prendre accions com el desenvolupament de la reproducció en captivitat i el control de la pesca. Una de les eines més interessants per al seu ús en la biologia de la conservació és la criopreservació d'espermatozoides, que presenta diversos avantatges per a aquesta espècie, incloent la sincronització de gàmetes, la selecció de línies genètiques o el seu ús per a la creació d'un criobanc. No obstant això, el desenvolupament de protocols de criopreservació necessàriament requereixen esperma de bona qualitat. A més, es necessita un mètode precís per avaluar la qualitat de l'esperma tant abans com després de la criopreservació. Sobre aquesta última qüestió, la motilitat dels espermatozoides dels peixos es considera un dels millors biomarcadors per a l'avaluació de la qualitat dels espermatozoides en els peixos, i es pot estudiar de forma subjectiva o objectiva utilitzant sistemes "computer assisted sperm analysis" (CASA-Mot). Primer, es va realitzar un experiment per avaluar la precisió i l'exactitud de tots dos mètodes per estudiar la motilitat de l'esperma: el mètode subjectiu i la tècnica objectiva que utilitza el sistema CASA-Mot. A més, es va provar si el grau d'experiència dels tècnics en el cas del mètode subjectiu té un efecte en la precisió de l'estimació de la motilitat i, per tant, hi ha una influència del personal del laboratori en l'avaluació de la motilitat del esperma. Vam concloure que tant el mètode com l'experiència tècnica eren factors clau per avaluar amb precisió la motilitat de l'esperma en l'anguila europea, de manera que es requereix l'ús de CASA-Mot juntament amb material qualificat per obtenir resultats fefaents. En segon lloc, es van avaluar mètodes alternatius per a la maduració dels mascles d'anguila europeus provant dos tractaments hormonals diferents: OVI, un gonadotropina recombinant; i VET, un gonadotropina purificada a partir d'orina femenina. Després de triar el millor tractament hormonal dels dos, es va avaluar l'efecte de tres dosis diferents amb l'objectiu d'obtenir el major rendiment al menor cost. Els resultats d'aquest experiment van apuntar a OVI com el millor tractament hormonal en una dosi setmanal de 1.5 UI/g de peix, que proporciona la major rendibilitat, obtenint esperma d'alta qualitat a un preu millor. En un tercer experiment, i utilitzant els coneixements adquirits en els dos primers experiments, es van realitzar una sèrie d'experiments per estandarditzar els protocols de criopreservació d'esperma d'anguila europea disponibles en aquest moment (utilitzant DMSO o metanol com crioprotector). Els resultats van apuntar al protocol que utilitza el metanol com el millor d'ells dos en termes de motilitat, velocitat i viabilitat dels espermatozoides i la preservació de la integritat de l'ADN. Seguint aquest últim mètode estandarditzat, es va realitzar un quart experiment amb l'objectiu de millorar el protocol en termes de volum (volums d'esperma més grans) i de qualitat espermàtica. A més, es va desenvolupar un protocol simple d'emmagatzematge a curt termini per complementar les opcions de preservar l'esperma durant diferents períodes de temps. De totes les condicions d'emmagatzematge provades, les dilucions 1/50 a 4ºC van mostrar els millors resultats, mantenint la motilitat en comparació amb el control durant 3 dies, i mantenint certa motilitat espermàtica (12%) després de 7 dies. A partir de l'experiment de criopreservació, va ser possible augmentar els volums a 2 i 5 ml sense perdre la qualitat de l'esperma en comparació amb volums més petits. / [EN] In the last decades, the European eel Anguilla anguilla has suffered a drastic decrease in the recruitment in most areas of their distribution range, leading the species to be included as critically endangered in the IUCN list. This situation, together with the high commercial importance of the species, evidence the need of taking actions such as development of reproduction in captivity and control of fisheries based on the complexity of their life cycle. One of the most interesting tools for its use in conservation biology is the sperm cryopreservation, which presents several advantages for this species such as the synchronization of gametes, selection of genetic lines or cryobanking. However, the development of cryopreservation protocols necessarily requires good quality sperm, and it is also needed an accurate method to assess sperm quality both pre- and post-cryopreservation. On this last matter, fish sperm motility is considered one of the best quality biomarkers for sperm quality assessment in fish, and it can be evaluated subjectively or objectively using computer assisted sperm analysis (CASA-Mot) systems. First, an experiment was conducted to evaluate the precision and accuracy of both methods for assessing sperm motility: the subjective method and the objective technique using CASA-Mot system. Moreover, it was tested whether the degree of expertise of the technicians in the case of the subjective method, has an effect on the accuracy of the motility estimation, and therefore there is an influence of the laboratory staff on the sperm motility assessment. Here we concluded that both the method and the technician expertise were key factors in order to accurately assess sperm motility in European eel, so the use of CASA-Mot together with qualified stuff is required to obtain reliable results. Secondly, and alternative methods for European eel males maturation was evaluated by testing two different hormonal treatments: OVI, a recombinant ¿-choriogonadotropin; and VET, a human chorionic gonadotropin purified from female urine. After choosing the best hormonal treatment, the effect of three different doses was evaluated aiming for best performance and lowest cost on the treatment. The results of this experiment pointed at OVI as the best hormonal treatment in terms on sperm quantity and quality in most of the weeks of treatment, and at a weekly dose of 1.5 IU/g fish, which also provide the greatest profitability, obtaining high quality sperm at a lower price. In a third experiment, and using the knowledge acquired in the two first experiments (using the OVI hormonal treatment and CASA-Mot to assess sperm quality), a series of experiments were conducted to standardize the European eel sperm cryopreservation protocols available at the moment (using DMSO or methanol as cryoprotectant). The results indicated that the protocol using methanol was the best of them two in terms of sperm motility and velocity, sperm viability and preservation of DNA integrity. Following this last standardized method, a fourth experiment was conducted aiming for improvement of the protocol in terms of volume (larger volumes) and sperm quality outcome. Moreover, a simple protocol for short-term storage was developed to complement the options to preserve sperm for different time periods. Of all the tested storing conditions, 1/50 dilutions at 4 ºC showed the best results, maintaining the motility compared to control for 3 days, and some sperm motility (12%) was still observed after 7 days. From the cryopreservation experiment, it was possible to scale up the cryopreserved volumes to 2 and 5 mL without losing sperm quality compared to lower volumes. Moreover, the protocol was further improved by supplementing the protocol with egg yolk as an additive, obtaining the highest cryopreserved sperm motilities (over 50%) ever reported in European eel. / Herranz Jusdado, JG. (2019). Improvement of techniques for sperm evaluation and cryobanking in European eel [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/130846 / TESIS

Artificial insemination (AI) with sex-sorted bottlenose dolphin spermatozoa provides female calves for obtaining more cohesive social groups and optimum genetic management of captive populations. However, distance of animals to the sorting facility represents a limit to the procedure. Although one bottlenose dolphin calf has been born using spermatozoa from frozen-thawed, sorted and recryopreserved spermatozoa, critical evaluation of the steps involved in this process is required to maximize its efficiency for future AIs and expansion of the technology to other species. Two experiments were designed to determine the efficiency of the sorting process and the quality of frozen-thawed bottlenose dolphin spermatozoa during sorting and recryopreservation. In experiment 1, the effect of two washing media (with and without 4 percent egg yolk, v/v) following density gradient centrifugation (DGC) on sperm recovery rate and in vitro characteristics of cryopreserved spermatozoa was examined. In experiment 2, cryopreserved semen was used to compare the effects of two recryopreservation methods (conventional straw freezing and directional freezing) on in vitro sperm characteristics of control (non-sorted) and sorted spermatozoa. Egg yolk supplementation of the washing medium in experiment 1 did not influence (P > 0.05) the sperm recovery rate, however, sperm motility parameters and viability were improved (P < 0.05). For Experiment 2, motility parameters and viability were influenced by stage of sex-sorting process, sperm type (non-sorted and sorted) and freezing method (P < 0.05). After recryopreservation, sorted spermatozoa frozen with the directional freezing method maintained higher (P < 0.05) motility parameters over the 24 h incubation period compared to spermatozoa frozen using straws. Quality of sperm DNA of nonsorted spermatozoa, as assessed by the SCSA, remained unchanged throughout the process. However, a possible interaction between Hoechst 33342 and acridine orange was observed in sorted samples. After recryopreservation, viability of sorted spermatozoa was higher (P < 0.05) than that of non-sorted spermatozoa across all time points. The percentages of viable spermatozoa determined by light (eosin-nigrosin) and fluorescence microscopy (propidium iodide) techniques were correlated (R^2=0.79, P < 0.001). Collective results indicate that bottlenose dolphin spermatozoa undergoing cryopreservation, sorting and recryopreservation are of adequate quality for use in AI.

CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior / Os objetivos deste estudo foram: 1) avaliar os aspectos da interaÃÃo das Binder of SPerm proteins (BSP) presentes no plasma seminal de caprinos e as principais proteÃnas do leite; 2) determinar se as BSP homÃlogas do plasma seminal de equinos, suÃnos e ovinos possuem propriedades de ligaÃÃo as proteÃnas do leite semelhante Ãs BSP bovinas; 3) investigar a interaÃÃo das proteÃnas do plasma seminal de caprinos e os componentes dos diluidores à base de lecitina de soja; 4) identificar as proteÃnas do plasma seminal de touros Curraleiro (PÃ-duro) associadas à circunferÃncia escrotal e os parÃmetros seminais. Para tanto, o leite desnatado tratado termicamente foi incubado com as proteÃnas do plasma seminal de caprinos e, aplicados em coluna cromatogrÃfica de gel filtraÃÃo na presenÃa e na ausÃncia de cÃlcio. AlÃm disso, o leite desnatado foi fracionado em duas fraÃÃes, MF-1 (proteÃnas do soro de leite) e MF-2 (caseÃnas), e posteriormente incubadas com as proteÃnas do plasma seminal de caprinos, seguida pela aplicaÃÃo em coluna de gel filtraÃÃo. As fraÃÃes foram eluÃdas e analisadas por Western blot. Adicionalmente, outras anÃlises foram realizadas para avaliar as propriedades desta ligaÃÃo. No primeiro procedimento, uma placa de ELISA foi sensibilizada com leite desnatado tratado termicamente e, em seguida, incubadas com diluiÃÃes em sÃrie de BSP purificadas e plasma seminal caprino, seguido por incubaÃÃo com anticorpos primÃrio e secundÃrios. Na segunda anÃlise, o leite desnatado, caseÃnas, &#945;-lactalbumina, &#946;-lactoglobulina diluÃdas em sÃrie foram gotejadas sobre uma membrana de nitrocelulose e, posteriormente, as membranas foram incubadas com plasma seminal de caprinos. A interaÃÃo foi detectada pela incubaÃÃo com anticorpos primÃrios e secundÃrios. No terceiro experimento, os espermatozoides epididimÃrios foram incubados com: (1) citrato/glicose + plasma seminal caprino, (2) plasma seminal caprino + diluidor leite, e (3) diluidor leite + plasma seminal de caprino. ApÃs o perÃodo de incubaÃÃo, as proteÃnas da membrana de espermatozoides foram extraÃdas e analisadas por Western blot. No segundo estudo, o leite desnatado foi incubado com as proteÃnas do plasma seminal de bovino, equino, suÃno e ovino, separadamente, e em seguida, foram aplicados em coluna cromatografia de filtraÃÃo em gel. AlÃm disso, a interaÃÃo de componentes de diluidores à base de lecitina de soja (Andromed e BioxcellÂ) foi investigada por cromatografia de filtraÃÃo em gel e ultracentrifugaÃÃo. Uma alÃquota de diluidor à base de lecitina de soja foi incubada com as proteÃnas do plasma seminal de caprinos e aplicadas em coluna de gel filtraÃÃo. As fraÃÃes foram eluÃdas e, apÃs este procedimento, as amostras foram analisadas por Western blot. A anÃlise por ultracentrifugaÃÃo foi realizada na ausÃncia e na presenÃa de vesÃculas de fosfolipÃdios oriundas de diluidores a base de lecitina de soja, Andromed e BioxcellÂ. As vesÃculas isoladas foram incubadas com as proteÃnas do plasma seminal de caprino. ApÃs a ultracentrifugaÃÃo, a presenÃa de BSP no sobrenadante e no sedimento foi analisada por Western Blot. Adicionalmente, o plasma seminal de dez touros Curraleiro (PÃ-duro) foi analisado por 2-D eletroforese. Os gÃis corados por Coomassie foram analisados no aplicativo PDQuestÂ. Nossos resultados demonstraram que as proteÃnas de BSP do plasma seminal caprino se ligam Ãs proteÃna do leite, especialmente, as caseÃnas e &#946;-lactoglobulina. AlÃm disso, estas proteÃnas interagem com as vesÃculas de fosfolipÃdios presentes nos diluidores Andromed e BioxcellÂ. As BSP de bovinos, equinos e suÃnos tambÃm se ligam aos componentes do leite. Jà as BSP de ovinos nÃo interagem com os componentes do leite desnatado. Nossas analises demonstraram que vinte e sete spots proteÃcos se correlacionam com pelo menos um parÃmetro reprodutivo. Em resumo, nossos resultados indicam que as BSP de caprinos se ligam Ãs proteÃnas do leite e aos fosfolipÃdios do diluidor Andromed e BioxcellÂ. Isto sugere que estes componentes tÃm um papel significativo na proteÃÃo de espermatozoide de caprinos, pois sequestram as BSP presentes no sÃmen. Nossos resultados sugerem que as BSP homÃlogas presentes no plasma seminal de equinos e suÃnos apresentam propriedades de ligaÃÃo Ãs proteÃnas do leite semelhantes Ãs BSP bovinas. AlÃm disso, o plasma seminal de touros Curraleiro (PÃ-duro) tem potenciais proteÃnas relacionadas com parÃmetros de qualidade seminal. Estes resultados sÃo de grande interesse, visto que elucida aspectos relacionados aos mecanismos de proteÃÃo dos espermatozoides pelos diluidores, para o desenvolvimento de novos diluidores livre de produtos de origem animal e na identificaÃÃo de proteÃnas com potencial à marcadores de fertilidade no plasma seminal de bovino. / The objectives of this study were: 1) to evaluate aspects of interaction between goat seminal plasma proteins and milk proteins; 2) to determine if homolog Binder of Sperm Proteins (BSP) from stallion, boar and ram seminal share the binding properties of the bovine BSP for the milk proteins; the mechanism of bovine sperm protection by milk is similar in different species of mammals; 3) to investigate the interactions of BSP proteins present in goat seminal plasma and phospholipids from soybean lecithin-based extender; 4) to identify seminal plasma proteins associated with scrotal circumference and sperm parameters. Heated skimmed milk was incubated with goat seminal plasma proteins and loaded onto Sepharose CL-4B column both in the presence and absence of calcium. Fractions were eluted and evaluated by Western blots using anti-goat BSP antibodies. Also, we fractionated milk into two fractions, MF-1 (mostly whey proteins) and MF-2 (mostly caseins), which were incubated with goat seminal plasma proteins and passed through gel filtration columns. Eluted fractions were then analysed by immunoblotting with anti-BSP antibodies. In addition, a series of analysis was conducted to evaluate binding properties involving milk and seminal plasma proteins. In the first procedure, an ELISA plate was saturated with heated skimmed milk and then incubated with serial dilutions of purified BSP proteins, goat seminal plasma proteins and anti-goat BSP. In a second analysis, heated skimmed milk, casein, &#945;-lactalbumin and &#946;-lactoglobulin were spotted onto a nitrocellulose membrane with serial dilutions. Membranes were then overlaid with goat seminal plasma proteins. Binding between milk and seminal plasma components were detected by successive incubations with primary and secondary antibodies. A third set of analysis was conducted to evaluate interactions among ejaculated and caudal epididymal sperm, milk and goat seminal plasma proteins. Epididymal sperm from each animal was incubated with: (1) citrate-glucose medium followed by seminal plasma; (2) with seminal plasma followed by milk extender; (3) with milk extender followed by seminal plasma (Fig. 1). Both ejaculated and epididymal goat sperm were also incubated with citrate-glucose medium without seminal plasma, as positive and negative controls, respectively. Following incubations, sperm membrane proteins were extracted and the presence of goat BSP proteins was assessed by Western blot Furthermore, heated skim milk was incubated with seminal plasma proteins from bulls, stallions, boars and rams and then loaded onto gel filtration column. The proteins were eluted and fractions were analysed by immunoblotting. Moreover, the interaction of hospholipids vesicles from soybean lecithin-based extender (Andromed and BioxcellÂ) and goat BSP proteins was investigated by gel filtration chromatography and ultracentrifugation analysis. An appropriate volume of soybean-based extender was incubated with goat seminal plasma proteins and passed through a gel filtration column. Proteins were eluted and fractions analysed by Western blot. Ultracentrifugation analysis was performed in the absence or in the presence of phospholipid vesicles. These vesicles were isolated from soybean lecithin extender and incubated with goat seminal proteins. The presence of goat BSP proteins in the supernatant and in the pellet was assessed by Western blot. In addition, seminal samples from ten Curraleiro Bulls were subjected to 2-D electrophoresis and Coomassie blue-stained gels analyzed with PDQuest software. Our results demonstrated that goat BSP proteins bound to milk protein, specially caseins and &#946;-lactoglobulin. In addition, these proteins interact with phospholipids vesicles of Andromed and BioxcellÂ. Bull, stallion and boar BSP proteins also bind to milk protein, whereas ram BSP proteins did not bind. Also, we identified that twenty and seven protein spots presented significant correlation with at least one reproductive parameter. In summary, our results indicate that goat BSP proteins bind to milk proteins and phospholipids from Andromed and Bioxcell semen extender. This suggests that these components play a significant role in protecting goat sperm by sequestrating all BSP proteins in semen. We also demonstrated that BSP homologs in boar, stallion seminal plasma share the binding properties of the bovine BSP for the milk proteins. Additionally, Curraleiro seminal plasma has potential proteins related to quality sperm parameters and they should be tested as putative fertility markers. These findings are of considerable interest in view of the mechanisms of sperm protection by extender constituents, for the development of novel extender free of animal components and the identification of proteins as potential biomarkers of fertility in bovine seminal plasma.

White Crappie (Pomoxis annularis) and Black Crappie (P. nigromaculatus) are popular North American gamefish; however, frequent fluctuations in year class strength present a management challenge for recreational fisheries. Intensive aquaculture production has the potential to address this challenge through controlled hatchery reproduction for supplemental stocking, but further study is needed to refine and optimize techniques. Therefore, this study evaluated the effects of hormone injection timing on latency period and spawning success, examined effective cryopreservation techniques for black-stripe Black Crappie sperm (a preferred hatchery phenotype), and compared simulated spring duration on out-of-season spawning success. Latency period for White Crappie did not depend on the diel time of gonadotrophin-releasing hormone injection. Cryopreservation of black-stripe Black Crappie sperm and subsequent fertilization of White Crappie eggs was more effective using 5% dimethyl-sulfoxide than 10% methanol. A longer duration at final spring spawning conditions (3 vs. 2 weeks) increased egg fertilization in out-of-season spawning experiments.

Many primate populations face the threat of extinction due to habitat loss, intensive agriculture, hunting for meat, the pet trade and/or use in traditional medicines. An alternative approach to in situ conservation includes gene banking and the use of assisted reproductive technologies (ART), such as oocyte in vitro maturation (IVM) and in vitro fertilization (IVF). Although many of these 'high-tech' solutions have not yet been proven viable for pragmatic wildlife conservation, basic research and development of these emerging tools can provide necessary information needed to optimize these techniques and institute ART as a routine practice in conservation efforts. A severely limiting factor in the successful application of ARTs is the availability of mature developmentally competent oocytes. Oocyte maturation involves many nuclear and cytoplasmic factors, which can be affected by maturation conditions and female age. In vitro maturation does not have the same success rate across species studied. In primates especially, IVM oocytes exhibit reduced developmental capacity upon fertilization when compared to in vivo matured (IVO) oocytes. This study aimed to investigate possible causes of reduced developmental capacity of primate IVM oocytes using the rhesus macaque (Macaca mulatta) as a model. Research efforts included investigation of ovarian senescence, oocyte karyotype and spindle morphology, and establishment of an optimal sperm cryopreservation protocol for use in IVF. Histological examination of the rhesus ovary demonstrated an age-related pattern of follicle depletion similar to that described in the human ovary. Oocyte karyotype analysis revealed a significant effect of IVM on the frequency of hyperhaploidy. In addition, immunostaining and confocal microscopy demonstrated a significant increase of anomalous chromosome congression on the oocyte metaphase II spindle equator in relation to IVM and donor female age. These results indicate that IVM can produce serious, if not lethal consequences for embryo development. This study presents baseline data on ovarian aging in the rhesus macaque and aspects of nuclear maturation during macaque IVM that may contribute to the design of primate oocyte recovery plans. Implementation of either of two sperm cryopreservation methods originally developed for rhesus and vervet monkeys will aid future investigation of the developmental capacity of IVM oocytes.

As espécies reativas de oxigênio são fundamentais na fisiologia espermática. No entanto, um desequilíbrio entre a produção e a capacidade antioxidante caracteriza o estresse oxidativo (EO). O espermatozoide é extremamente suscetível ao EO pois, dentre outras características, a membrana plasmática é rica em ácidos graxos poli-insaturados responsáveis por promoverem a fluidez necessária em processos fisiológicos como motilidade e fertilização. Por outro lado, essas insaturações são mais facilmente oxidadas e vulneráveis à peroxidação lipídica. Em função desta susceptibilidade, estas células dependem fortemente de compostos presentes no plasma seminal (PS) para a proteção contra esse evento. Dessa forma, a carnosina, dipeptídeo presente no PS pode ser uma das responsáveis pela proteção contra o acúmulo do MDA. No entanto, durante a criopreservação do sêmen equino é necessário retirar o PS. Em estudo recente, verificamos que esta remoção, torna os espermatozoides sensíveis ao subproduto extremamente deletério da peroxidação lipídica, o malondialdeído (MDA). Como a carnosina é removida junto com o plasma seminal durante a criopreservação, foram desenvolvidos 2 experimentos sequenciais visando a melhora da qualidade do sêmen criopreservado com adição de carnosina. Amostras de sêmen de sete garanhões foram tratadas com concentrações crescentes de carnosina adicionadas ao diluidor (1mM, 50mM e 100mM). Após a descongelação, as amostras foram divididas retrospectivamente em grupos de alta congelabilidade (AC: motilidade maior que 30%) e baixa congelabilidade (BC: motilidade menor que 30%). Amostras tratadas com 50mM apresentaram menor porcentagem de células com lesão de membrana plasmática e, quando tratadas com 100mM, células com maior amplitude do deslocamento lateral de cabeça. Amostras controle BC apresentaram menor porcentagem de células com DNA íntegro em relação às amostras AC. No entanto, houve um leve aumento na porcentagem de células com DNA íntegro em amostras BC com 100mM, não diferindo das amostras AC. Por outro lado, amostras BC criopreservadas com 50mM apresentaram maiores porcentagens de células com escore calculado de potencial de membrana mitocondrial e mais suscetíveis ao EO em relação ao controle. Apesar da proteção parcial, a maior suscetibilidade à peroxidação lipídica torna-se um problema, especialmente pelo fato de que espermatozoides equinos são mais suscetíveis ao MDA. Um motivo para este efeito seria a afinidade da carnosina em reagir com açúcares, o que poderia influenciar negativamente a atividade mitocondrial e o status oxidativo, ao diminuir a produção de piruvato pela via glicolítica. Desta forma, no experimento 2, amostras BC foram tratadas com a combinação de carnosina (0 e 50mM) e piruvato (0 e 5mM) em arranjo fatorial 2x2. Verificou-se que o tratamento com piruvato (5mM) proporcionou menos células com baixa atividade mitocondrial. Por outro lado, a carnosina (50mM), promoveu maior motilidade total, progressiva e células rápidas. Houve uma tendência de aumento nas células com velocidade progressiva e atividade mitocondrial na combinação de tratamentos. Não houve diferença entre os grupos na suscetibilidade ao EO que, no entanto, correlacionou-se negativamente com células móveis, rápidas e integridade de membrana plasmática e acrossomal. Estes resultados indicam que subprodutos da peroxidação lipídica, sendo o principal deles o MDA, podem causar danos ao DNA, às mitocôndrias e à cinética espermática. Neste contexto, a carnosina (100mM) parece ter um leve efeito protetor ao DNA contra o acúmulo de MDA. Além disto, 50mM de carnosina parece auxiliar na manutenção da velocidade progressiva e atividade mitocondrial quando associada ao piruvato (5mM). Assim, a carnosina e o piruvato podem ser utilizados na prevenção de crioinjúrias em amostras de baixa congelabilidade. / Reactive oxygen species (ROS) plays a key role in the sperm physiology. However, an imbalance between ROS production and antioxidant capacity characterize the oxidative stress (OE). The spermatozoa are extremely susceptible to EO because, among other characteristics, the plasma membrane is rich in polyunsaturated fatty acids responsible for promoting fluidity necessary in physiological processes such as motility and fertilization. However, these unsaturations are more easily oxidized and vulnerable to lipid peroxidation. Due to this susceptibility, these cells strongly depend on compounds present in the seminal plasma (SP) to protect against this event. Thus, carnosine, a dipeptide present in SP of stallions, may be a key factor on the protection against MDA accumulation. Nevertheless, during the equine sperm cryopreservation process, SP is removed. In a recent study, we observed that seminal plasma removal led to an increased susceptibility of equine spermatozoa to extremely deleterious product of lipid peroxidation, malondialdehyde (MDA). As the carnosine is removed together with the seminal plasma during cryopreservation, two sequential experiments were developed aiming to improve the quality of stallion cryopreserved semen by means of carnosine therapy. Samples from seven stallions were treated with increasing concentrations of carnosine added to the extender (1mM, 50mM and 100mM) and submitted to cryopreservation. After thawing, samples were classified as high freezeability (HF: total motility greater than 30%) and low freezeability (LF: total motility lower than 30%). Samples treated with 50mM presented lower percentage of sperm showing plasma membrane damage and, when treated with 100mM, a greater amplitude of the lateral head displacement was observed. Untreated LF samples showed a lower percentage of cells showing intact DNA in relation to HF samples. By contrast, when LF samples were treated with 100mM, there was an increase in the percentage of cells with intact DNA, which was similar to the HF samples. On the other hand, LF samples cryopreserved with 50mM had a higher percentage of cells showing high calculated mitochondrial membrane potential score and increased susceptibility to OE in relation to the control. Despite the partial protection, the increased susceptibility to lipid peroxidation is a concern since equine spermatozoa is highly vulnerable to the MDA. Those results could be due to the affinity of carnosine to react with sugars, which could negatively influence mitochondrial activity and an oxidative state by decreasing pyruvate production. Hence, in experiment 2, LF samples were treated with a combination of carnosine (0 and 50mM) and pyruvate (0 and 5mM) in a 2x2 factorial arrangement. We observed that samples treated with pyruvate (5mM) had decreased percentage of cells with low mitochondrial activity. On the other hand, carnosine (50mM) increased total motility, progressive motility and fast cells. We also observed a tendency to increased progressive velocity and mitochondrial activity in the combination of treatments. There was no difference on sperm susceptibility to OE between treatments. However, this variable correlated negatively with the percentage of motile and rapid cells as well as those showing intact membrane and acrosome. These results indicate that the byproduct of lipid peroxidation (MDA) may cause damage to DNA, mitochondria and sperm kinetics. In this context, carnosine (100mM) appears to have a mild protective effect on DNA against the accumulation of MDA. Furthermore, 50mM of carnosine seems to improve progressive velocity and mitochondrial activity when associated with pyruvate (5mM). Thus, carnosine and pyruvate can be used on cryoinjuries prevention in low freezeability samples.

As espécies reativas de oxigênio são fundamentais na fisiologia espermática. No entanto, um desequilíbrio entre a produção e a capacidade antioxidante caracteriza o estresse oxidativo (EO). O espermatozoide é extremamente suscetível ao EO pois, dentre outras características, a membrana plasmática é rica em ácidos graxos poli-insaturados responsáveis por promoverem a fluidez necessária em processos fisiológicos como motilidade e fertilização. Por outro lado, essas insaturações são mais facilmente oxidadas e vulneráveis à peroxidação lipídica. Em função desta susceptibilidade, estas células dependem fortemente de compostos presentes no plasma seminal (PS) para a proteção contra esse evento. Dessa forma, a carnosina, dipeptídeo presente no PS pode ser uma das responsáveis pela proteção contra o acúmulo do MDA. No entanto, durante a criopreservação do sêmen equino é necessário retirar o PS. Em estudo recente, verificamos que esta remoção, torna os espermatozoides sensíveis ao subproduto extremamente deletério da peroxidação lipídica, o malondialdeído (MDA). Como a carnosina é removida junto com o plasma seminal durante a criopreservação, foram desenvolvidos 2 experimentos sequenciais visando a melhora da qualidade do sêmen criopreservado com adição de carnosina. Amostras de sêmen de sete garanhões foram tratadas com concentrações crescentes de carnosina adicionadas ao diluidor (1mM, 50mM e 100mM). Após a descongelação, as amostras foram divididas retrospectivamente em grupos de alta congelabilidade (AC: motilidade maior que 30%) e baixa congelabilidade (BC: motilidade menor que 30%). Amostras tratadas com 50mM apresentaram menor porcentagem de células com lesão de membrana plasmática e, quando tratadas com 100mM, células com maior amplitude do deslocamento lateral de cabeça. Amostras controle BC apresentaram menor porcentagem de células com DNA íntegro em relação às amostras AC. No entanto, houve um leve aumento na porcentagem de células com DNA íntegro em amostras BC com 100mM, não diferindo das amostras AC. Por outro lado, amostras BC criopreservadas com 50mM apresentaram maiores porcentagens de células com escore calculado de potencial de membrana mitocondrial e mais suscetíveis ao EO em relação ao controle. Apesar da proteção parcial, a maior suscetibilidade à peroxidação lipídica torna-se um problema, especialmente pelo fato de que espermatozoides equinos são mais suscetíveis ao MDA. Um motivo para este efeito seria a afinidade da carnosina em reagir com açúcares, o que poderia influenciar negativamente a atividade mitocondrial e o status oxidativo, ao diminuir a produção de piruvato pela via glicolítica. Desta forma, no experimento 2, amostras BC foram tratadas com a combinação de carnosina (0 e 50mM) e piruvato (0 e 5mM) em arranjo fatorial 2x2. Verificou-se que o tratamento com piruvato (5mM) proporcionou menos células com baixa atividade mitocondrial. Por outro lado, a carnosina (50mM), promoveu maior motilidade total, progressiva e células rápidas. Houve uma tendência de aumento nas células com velocidade progressiva e atividade mitocondrial na combinação de tratamentos. Não houve diferença entre os grupos na suscetibilidade ao EO que, no entanto, correlacionou-se negativamente com células móveis, rápidas e integridade de membrana plasmática e acrossomal. Estes resultados indicam que subprodutos da peroxidação lipídica, sendo o principal deles o MDA, podem causar danos ao DNA, às mitocôndrias e à cinética espermática. Neste contexto, a carnosina (100mM) parece ter um leve efeito protetor ao DNA contra o acúmulo de MDA. Além disto, 50mM de carnosina parece auxiliar na manutenção da velocidade progressiva e atividade mitocondrial quando associada ao piruvato (5mM). Assim, a carnosina e o piruvato podem ser utilizados na prevenção de crioinjúrias em amostras de baixa congelabilidade. / Reactive oxygen species (ROS) plays a key role in the sperm physiology. However, an imbalance between ROS production and antioxidant capacity characterize the oxidative stress (OE). The spermatozoa are extremely susceptible to EO because, among other characteristics, the plasma membrane is rich in polyunsaturated fatty acids responsible for promoting fluidity necessary in physiological processes such as motility and fertilization. However, these unsaturations are more easily oxidized and vulnerable to lipid peroxidation. Due to this susceptibility, these cells strongly depend on compounds present in the seminal plasma (SP) to protect against this event. Thus, carnosine, a dipeptide present in SP of stallions, may be a key factor on the protection against MDA accumulation. Nevertheless, during the equine sperm cryopreservation process, SP is removed. In a recent study, we observed that seminal plasma removal led to an increased susceptibility of equine spermatozoa to extremely deleterious product of lipid peroxidation, malondialdehyde (MDA). As the carnosine is removed together with the seminal plasma during cryopreservation, two sequential experiments were developed aiming to improve the quality of stallion cryopreserved semen by means of carnosine therapy. Samples from seven stallions were treated with increasing concentrations of carnosine added to the extender (1mM, 50mM and 100mM) and submitted to cryopreservation. After thawing, samples were classified as high freezeability (HF: total motility greater than 30%) and low freezeability (LF: total motility lower than 30%). Samples treated with 50mM presented lower percentage of sperm showing plasma membrane damage and, when treated with 100mM, a greater amplitude of the lateral head displacement was observed. Untreated LF samples showed a lower percentage of cells showing intact DNA in relation to HF samples. By contrast, when LF samples were treated with 100mM, there was an increase in the percentage of cells with intact DNA, which was similar to the HF samples. On the other hand, LF samples cryopreserved with 50mM had a higher percentage of cells showing high calculated mitochondrial membrane potential score and increased susceptibility to OE in relation to the control. Despite the partial protection, the increased susceptibility to lipid peroxidation is a concern since equine spermatozoa is highly vulnerable to the MDA. Those results could be due to the affinity of carnosine to react with sugars, which could negatively influence mitochondrial activity and an oxidative state by decreasing pyruvate production. Hence, in experiment 2, LF samples were treated with a combination of carnosine (0 and 50mM) and pyruvate (0 and 5mM) in a 2x2 factorial arrangement. We observed that samples treated with pyruvate (5mM) had decreased percentage of cells with low mitochondrial activity. On the other hand, carnosine (50mM) increased total motility, progressive motility and fast cells. We also observed a tendency to increased progressive velocity and mitochondrial activity in the combination of treatments. There was no difference on sperm susceptibility to OE between treatments. However, this variable correlated negatively with the percentage of motile and rapid cells as well as those showing intact membrane and acrosome. These results indicate that the byproduct of lipid peroxidation (MDA) may cause damage to DNA, mitochondria and sperm kinetics. In this context, carnosine (100mM) appears to have a mild protective effect on DNA against the accumulation of MDA. Furthermore, 50mM of carnosine seems to improve progressive velocity and mitochondrial activity when associated with pyruvate (5mM). Thus, carnosine and pyruvate can be used on cryoinjuries prevention in low freezeability samples.

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