Resumo

Intracytoplasmic Sperm Injection (ICSI) has increased usage in cases of stallion fertility issues, particularly for older stallions, those with reduced sperm numbers or quality, or stallions that have passed away, and only a limited amount of frozen semen is available. By manipulating the frozen semen through thawing, diluting, and refreezing or by cutting the straw under liquid nitrogen, the supply of semen for ICSI can be extended. While ICSI requires a minimal number of spermatozoa per procedure, it is important to consider sperm quality as a crucial factor affecting fertilization and embryo development. Although it is possible to produce healthy embryos and offspring from low quality sperm samples, it is preferable to process and select morphologically and functionally superior sperm to maximize the chances of successful fertilization and embryo development. Several techniques are available for selecting the spermatozoa for ICSI, such as swim-up, washing, density gradient centrifugation, microfluidic sorting, and some combinations. In this review, we will focus on semen type, handling, recent breakthroughs, stallion effects on ICSI efficiency and the prospects of this technology within the equine industry.(AU)

Resumo

This study aimed to evaluate the efficiency of two or three estrus synchronizations followed by artificial insemination (AI) by laparoscopy with frozen semen in sheep. Santa Inês sheep (n=147) were randomly distributed into two groups: Re-sync - 2FTAI (n=72) and Doppler - 3FTAI (n=75), synchronized with a short protocol associated with GnRH and AI by laparoscopy with frozen semen 50 h after removing the P4 device (D0). Two AIs were performed in the Re-sync group, with the start of the resynchronization protocol on D23 and gestational diagnosis on D30; the non-pregnant females were inseminated again. The sheep were resynchronized (D10) in the Doppler group and the gestation diagnosis was made early at 17 days using Doppler ultrasound. The open females were inseminated again, totaling three inseminations in 42 days. Early gestation diagnoses were confirmed at 30 days. Re-sync (29.16%) and Doppler (21.33%) were similar to each other in terms of cumulative gestation rate (P>0.05). The indicators of the non-gestation diagnosis technique at 17 days were sensitivity of 100%, specificity of 28%, positive predictive value of 21.3%, negative predictive value of 100%, and accuracy of 39.8%. Early diagnosis allowed sheep to be inseminated two to three times in the same period and was effective in diagnosing truly non-pregnant females. Therefore, estrus resynchronization associated with AI by laparoscopy using frozen semen can be applied in sheep, but a higher gestation rate could not be achieved with two or three inseminations at the end of the breeding season.

Objetivou-se avaliar a eficiência de duas ou três sincronizações de estro seguida da inseminação artificial (IA) por laparoscopia com sêmen congelado em ovinos. As ovelhas Santa Inês (n=147) foram distribuídas aleatoriamente em 2 grupos: Re-sync - 2IATF (n=72) e Doppler - 3IATF (n=75), sincronizadas com protocolo curto associado ao GnRH e IA por laparoscopia com sêmen congelado 50 horas após a retirada do dispositivo P4 (D0). No grupo Re-sync foram realizadas duas IA com início do protocolo de ressincronização em D23 e diagnóstico gestacional em D30, as fêmeas não gestantes eram inseminadas novamente. No grupo Doppler as ovelhas foram ressincronizadas (D10) e o diagnóstico de gestação realizado precocemente aos 17 dias, com auxílio da ultrassonografa Doppler. As fêmeas vazias eram inseminadas novamente, totalizando três inseminações em 42 dias. Os diagnósticos precoces de gestação foram confirmados com 30 dias. Re-sync (29,16%) e Doppler (21,33%), foram semelhantes entre si na taxa de prenhez acumulativa (P>0,05). Os indicadores da técnica de diagnóstico de não-gestação aos 17 dias foram: sensibilidade 100%, especificidade 28%, valor preditivo positivo 21,3%, valor preditivo negativo 100% e acurácia 39,8%. Com o auxílio do diagnóstico precoce as ovelhas puderam ser inseminadas de duas a três vezes no mesmo período e mostrou efetividade em diagnosticar as fêmeas verdadeiramente não gestante. Conclui-se que a ressincronização de estro associada a IA por laparoscopia utilizando sêmen congelado pode ser aplicada em ovinos, entretanto não foi possível alcançar maior taxa de prenhez com duas ou três inseminações ao final da estação de monta.

Resumo

Cooling milt conserves viable spermatozoa to extend the period available for artificial fertilization and avoids the robust protocols and high costs associated with cryopreservation. Yet, the sperm quality curves of fresh and refrigerated milt have not yet been compared for pacu (Piaractus mesopotamicus), which is often used as a biological model. This study aimed to analyze the milt quality of male P. mesopotamicus across 24 h of refrigeration. Six adult males were induced with carp pituitary extract. Sperm movement, membrane integrity, and morphology was compared between extruded milt samples stored for 24 h under either ambient temperature or under refrigeration at 12.63 °C. Sperm motility differed significantly over time. After 24 h of storage, motility values were higher in refrigerated spermatozoa than in those kept at ambient temperature. Sperm cell survival rates did not differ 4­8 h post collection. After 16 h, refrigerated cells showed superior membrane integrity (82.05 ± 4.23%) compared to those stored at ambient temperature (66.98 ± 6.45%), maintaining this pattern up to 24 h. In terms of sperm morphology rate, milt from both treatment groups was still viable for use 8 h after collection. However, after 16 h of storage, both groups exhibited a large reduction in normality rates, and at 24 h, all milt were unfeasible. In conclusion, P. mesopotamicus milt can be stored up to 8 h after collection when refrigerated at 12.63 °C, without the use of extenders and/or cryoprotectants, maintaining enough quality for egg fertilization.

O resfriamento do sêmen mantém espermatozóides viáveis ​​para estender o período útil para fertilização artificial e evita o uso de protocolos robustos e altos custos associados à criopreservação. No entanto, as curvas de qualidade espermática do sêmen fresco e refrigerado ainda não foram comparadas para o pacu (Piaractus mesopotamicus), que é frequentemente usado como modelo biológico. Este estudo teve como objetivo analisar a qualidade do sêmen de P. mesopotamicus durante 24 horas de refrigeração. Seis machos adultos foram induzidos com extrato de hipófise de carpa. Os dados de movimento espermático, integridade da membrana e morfologia foram comparados entre amostras de sêmen armazenadas por 24 horas em temperatura ambiente ou sob refrigeração a 12,63 °C. A motilidade dos espermatozoides diferiu significativamente ao longo do tempo. Após 24 horas de armazenamento, os valores de motilidade foram maiores nos espermatozoides refrigerados do que naqueles mantidos em temperatura ambiente. As taxas de sobrevivência dos espermatozoides não diferiram em 4 e 8 h após a coleta. Após 16 h, as células refrigeradas apresentaram integridade de membrana superior (82,05 ± 4,23%) em comparação àquelas armazenadas em temperatura ambiente (66,98 ± 6,45%), mantendo esse padrão até 24 h. Em termos de taxa de morfologia espermática, o sêmen de ambos os tratamentos ainda era viável para uso 8 horas após a coleta. Porém, após 16 h de armazenamento, ambos os grupos apresentaram grande redução nas taxas de normalidade, e às 24 h, todo sêmen estava inviável. Conclui-se que o sêmen de P. mesopotamicus pode ser armazenado até 8 h após a coleta quando refrigerado a 12,63 °C, sem uso de diluentes e/ou crioprotetores, mantendo qualidade suficiente para a fertilização de ovócitos.

Resumo

The objective of this research was to determine the influence of heat stress, using the temperature-humidity index (THI), on the production and quality of native sperm of bulls. The effect of heat stress on the quantity of semen (mL), density of ejaculate (number of spermatozoa, 106/mL), gross sperm motility (1-5), number of frozen doses, and motility after freezing was analysed in 1,017 sperm samples taken from 32 Holstein-Friesian bulls, in the 2017-2019 period, at the Centre for Reproduction and Embryo Transfer in Serbia. The lowest amount of ejaculate (4.18±1.95 mL) and the lowest density of ejaculate (1,189.19±668.23 × 106/mL) were recorded under conditions of very strong heat stress on the day of semen collection. The level of heat stress measured on the day of semen collection did not affect sperm gross motility, number of frozen doses, and motility after freezing. The level of heat stress at the beginning of spermatogenesis, measured 60 days before semen collection, did not affect the amount of ejaculate and motility of spermatozoa after freezing, but at very strong stress, the lowest density of ejaculate (1,170.34±680.27 × 106/mL) and gross motility of spermatozoa were found (2.91±0.96). The lowest number of doses per ejaculate was recorded in conditions of moderate heat stress (396.6±157.71). Bulls older than 36 months had the best results according to all tested parameters of native sperm production and quality. The year in which the bulls produced semen did not affect density of ejaculate and sperm motility. The season of semen collection did not significantly affect the production and quality of native sperm, due to the practice of exploiting only bulls with the best sperm quality during the summer.(AU)

Resumo

The present study evaluated the cryoprotectant efficacy of dimethylacetamide (DMA) and ethylene glycol in a one-step protocol to freeze boar sperm. The sperm-rich portion of the ejaculates from two boars were collected once a week, for 10 weeks. After collection, the ejaculates were diluted (1:1; v/v) in the cooling extender. After determining their spermatozoa concentration, the ejaculates were pooled with the same number of spermatozoa from each boar and stabilized at 20°C for 120 min. Distinct cryoprotectants were added to the cooling extender at 20 °C, at different concentrations, composing six treatments: 1.25% and 2.5% glycerol (control); 1.25% and 2.5% ethylene glycol; 2.5% and 5.0% DMA. The samples were stored in 0.25 mL straws, containing 35 × 106 spermatozoa. After 90 min at 20 °C, the straws were submitted to a cooling curve until 5 °C (0.3 to 0.5 °C/min) and kept at 5°C for 60 min. Freezing was conducted by placing the straws horizontally 5 cm above the liquid nitrogen for 10 min, followed by immersion on liquid nitrogen. After thawing at 37 °C for 30 seconds, sperm quality was evaluated through a computer-assisted semen analysis system and flow cytometry. Sperm motility was greater (P< 0.05) in treatments with 5.0% and 2.5% DMA (22.2 ± 2.6% and 20.0 ± 2.8%, respectively) than in treatment with 2.5% ethylene glycol (8.2 ± 1.0%). The integrity of the plasma membrane (P = 0.08) and mitochondrial membrane potential (P = 0.27) was similar among the treatments. The treatment with 2.5% ethylene glycol was the least efficient to maintain intact acrosome membrane (P< 0.01). Some kinetics parameters (DAP, DCL, DSL, VAP, VCL, VSL e ALH) were positively affected by 5.0% DMA. The one-step freezing protocol resulted in unsatisfactory boar sperm motility after thawing, regardless of the cryoprotectant.

O presente estudo objetivou avaliar a eficácia de um protocolo one-step de congelamento do sêmen suíno utilizando dimetilacetamida (DMA) e etilenoglicol como crioprotetores. Durante 10 semanas, a fração rica dos ejaculados de dois machos suínos foram coletados, uma vez por semana. Após a coleta, os ejaculados foram diluídos (1:1; v/v) no diluidor de resfriamento. Após a avaliação da concentração espermática, os ejaculados foram agrupados em um pool com o mesmo número de espermatozoides de cada macho e estabilizados a 20 °C por 120 min. Os criopropetores foram adicionados ao diluidor de congelamento a 20 °C, em diferentes concentrações, compondo seis tratamentos: glicerol (controle), 1,25% e 2,5%; etilenoglicol, 1,5% e 2,5%; e DMA, 2,5% e 5,0%. As amostras foram armazendadas em palhetas de 0,25 mL contendo 35 x 106 espermatozoides. Após 90 min a 20 °C as palhetas foram submetidas a uma curva de resfriamento até 5 °C (0,3 a 0,5 °C/mim) e mantidas a 5 °C por 60 min. O congelamento foi realizado a partir da colocação das palhetas horizontalmente a 5 cm acima do nitrogênio líquido por 10 min, com sua posterior imersão no nitrogênio líquido. Após o descongelamento a 37 °C por 30 segundos a qualidade espermática foi avaliada através de um sistema computadorizado e por citometria de fluxo. A motilidade espermática foi maior (P < 0,05) nos tratamentos com 5,0% e 2,5% DMA (22,2 ± 2,6% e 20,0 ± 2,8%, respectivamente) do que no tratamento com 2,5% etilenoglicol (8,2 ± 1,0%). A integridade da membrana plasmática (P = 0,08) e potencial de membrana mitocondrial (P = 0,27) foi similar entre os tratamentos. O tratamento com 2,5% de etilenoglicol foi menos eficiente em manter membrana acrossomal intacta (P< 0,01). Alguns parâmetros de cinética espermática (DAP, DCL, DSL, VAP, VCL, VSL e ALH) foram afetados positivamente pelo uso de DMA a 5.0%. O protocolo simplificado para congelamento de sêmen suíno resultou em motilidade espermática insatifatória após o descongelamento, independente do crioprotetor utilizado.

Resumo

Cryoprotectants are required to reduce damage caused to the cells due to low temperatures during the cryopreservation. Antifreeze proteins (AFP) have a well-known role in cell membrane protection, while resveratrol is a potent antioxidant. This study assessed the effect of the association of resveratrol concentrations and AFP I in a ram semen extender. Pooled semen of four rams was allocated into six treatments in a factorial arrangement: (CONT, only the semen extender); only AFP I (ANT: 0.1 µg/mL of AFP I), only resveratrol, one treatment with two levels (10 µM/mL or 50 µM/mL of resveratrol); and two treatments with the interactions, with one AFP I and one of the two levels of resveratrol (0.1 µg/mL of AFP I with 10 µM/mL resveratrol; 0.1 µg/mL of AFP I with 50 µM/mL resveratrol). No interaction between factors was observed on sperm kinetics, plasma membrane integrity, hypo-osmotic test, and mitochondrial activity parameters. There was a high probability (P = 0.06) of reducing sperm cells with functional membrane percentage in the hypo-osmotic test and increasing the percentage of sperm with high mitochondrial activity (P = 0.07) was observed in AFP presence. An interaction of AFP and resveratrol was observed in non-capacitated sperm (P = 0.009), acrosomal reaction (P = 0.034), and sperm binding (P = 0.04). In conclusion, the association of resveratrol and AFP did not improve the quality of frozen-thawed semen and even promoted deleterious effects compared to their single addition in the semen extender. The supplementation of 50 µM/mL of resveratrol improved the outcomes of frozen-thawed ram sperm, being a potential cryoprotectant.(AU)

Resumo

This study aimed to analyze the characteristics of the HSP70 gene and protein in spermatozoa of Bali bulls of different age groups and to examine its potential as a biomarker determining bull fertility. This study used frozen semen produced from six Bali bulls divided into two groups based on age (≤ 9 years and ≥ 12 years). Parameters of frozen semen quality analyzed included sperm motility and kinetics using computer-assisted semen analysis, sperm morphological defects using Diff-Quick staining, acrosome integrity using FITC-PNA staining, and DNA fragmentation using acridine orange staining. HSP70 gene expression characterization was analyzed using qRT-PCR, and HSP70 protein abundance was analyzed using enzyme immunoassays. Fertility field data were obtained by analyzing the percentage conception rate for each bull based on the artificial insemination service data contained in the Indonesian-integrated system of the National Animal Health Information System (iSIKHNAS). The results showed significant differences (P<0.05) in total and progressive motility, morphological defects of the neck and midpiece, and tail of sperm, and acrosome integrity between the age groups of Bali bulls. HSP70 gene expression and protein abundance showed no significant differences (P>0.05) in different age groups. HSP70 gene expression correlated with fertility rate (P<0.05). Age affected several semen quality parameters but did not affect HSP70 gene expression and protein abundance. The HSP70 gene molecule could be a biomarker that determines the fertility of Bali bulls.(AU)

Resumo

We evaluated the post-thaw development of in vitro-produced (IVP) bovine embryos cryopreserved using vitrification and slow-freezing techniques on different days after in vitro fertilization (IVF). Nine replicates of IVP were performed. Embryos at the expanded blastocyst stage with quality grades 1 and 2 (according to the International Embryo Technology Society (IETS) manual) were selected on days 7, 7.5, and 8 after IVF. Embryos (n = 472) were randomly divided and cryopreserved using slow freezing (n = 257) or vitrification (n = 215). The embryos were organized into six groups according to the cryopreservation technique and the day: 1) Group DT7 (embryos subjected to slow freezing on D7, n = 140); 2) Group DT7.5 (embryos subjected to slow freezing 12 hours after D7, on D7.5; n = 61); 3) Group DT8 (embryos subjected to slow freezing on D8, n = 56); 4) Group VIT7 (embryos vitrified on D7, n = 127); 5) Group VIT7.5 (embryos vitrified 12 hours after D7, on D7.5; n = 49); and 6) Group VIT8 (embryos vitrified on D8, n = 39). Data were arcsine-transformed and analyzed using analysis of variance and the GLIMMIX procedure in SAS (SAS 9.2), with P < 0.05. The re-expansion and embryo hatching rates were higher in vitrified embryos than in embryos subjected to slow freezing (P < 0.05). Embryo quality grade did not influence the total developmental rate (P > 0.05). However, grade 1 embryos re-expanded more rapidly (within 24 hours) than grade 2 embryos. Grade 1 embryos showed better results with vitrification than with slow freezing. The experimental groups represented a technique × day interaction and did not differ in terms of re-expansion and hatching rates (P > 0.05).(AU)

Avaliou-se o desenvolvimento pós-descongelamento de embriões bovinos produzidos in vitro (PIV) criopreservados pela técnica de vitrificação e de congelamento lento em diferentes dias após a fertilização in vitro (FIV). Foram realizadas 9 réplicas de PIV. Nos dias 7; 7,5 e 8 após a FIV, foram selecionados embriões no estágio de blastocisto expandido de grau de qualidade 1 e 2 (de acordo com o manual IETS). Os embriões (n=472) foram divididos aleatoriamente para serem criopreservados por congelamento lento (n=257) ou vitrificação (n=215). Organizou-se os embriões em 6 grupos de acordo com a técnica de criopreservação e o dia: 1) Grupo DT7 (embriões submetidos ao congelamento lento no D7, n= 140); 2) Grupo DT7,5 (embriões submetidos ao congelamento lento 12 horas após o D7, no D7,5; n= 61); 3) Grupo DT8 (embriões submetidos ao congelamento lento no D8, n=56); 4) Grupo VIT7 (embriões vitrificados no D7, n= 127); 5) Grupo VIT7,5 (embriões vitrificados 12 horas após o D7, no D7,5; n= 49); 6) Grupo VIT8 (embriões vitrificados no D8, n= 39). Os dados foram transformados para arcoseno e analisados por Análise de Variância utilizando o procedimento GLIMMIX do SAS (SAS 9.2) com P<0,05. A taxa de re-expansão e de eclosão embrionária foi maior para embriões vitrificados que para embriões submetidos ao congelamento lento (P<0,05). O grau de qualidade embrionária não influenciou as taxas de desenvolvimento totais (P>0,05). Porém embriões de grau 1 re-expandiram mais rapidamente (às 24 h) que embriões grau 2. Embriões grau 1 apresentaram melhores resultados com a técnica de vitrificação do que com congelamento lento. Os grupos experimentais representaram a interação técnica*dia e não diferiram entre si quanto as taxas de re-expansão e eclosão (P>0,05).(AU)

Resumo

The objective of the present study was to transpose sperm freezing methodology from domestic goat to the Tadjik markhor (Capra falconeri heptneri) and to address the feasibility to develop IVP and artificial insemination using such frozen semen. Semen of different adult markhor males were successfully recovered by electro-ejaculation and were then frozen using caprine methodology. Frozen semen showed good survival rates at thawing and good fertility rates were assessed in heterologous in vitro fertilization system with goat oocytes. LOPU/IVF was applied for Tadjik markhor females allowing the first successful blastocyst production in vitro. In an applied program, we also transposed successfully intrauterine AI method with frozen/thawed semen to the Tadjik markhor.AU)

Resumo

In cattle, artificial insemination (AI) is a technique that allows breeding by depositing frozen-thawed and extended semen into the female reproductive tract. The semen contains sperm with various motility patterns including dead, progressive and hyperactivated. Sperm hyperactivation is high amplitude, asymmetrical beating of sperm tail which usually occurs in the oviduct as part of the capacitation process, but it can also be induced by cryopreservation. After insemination, sperm enter the uterine glands and trigger a pro-inflammatory response in the uterus. Hyperactivated sperm, stimulated by sperm-Toll-like receptor 2 (TLR2), penetrates the mucus and uterine glands more efficiently and enhances the immune response. This facilitates the clearance of excess and dead sperm from the uterus. Some sperm escape the immune response and reach the oviduct either before or after the immune response is initiated. In the oviduct, sperm bind to the epithelium and form a reservoir. This triggers an anti-inflammatory response and preserves the fertilization potential of sperm. Hyperactivation facilitates sperm detaching from the epithelium, swimming through the viscous mucus and cumulus cells, and penetrating the egg's zona pellucida. Sperm-TLR2 activation enhances Ca2+-influx and acrosome reaction, which enables sperm to penetrate and fertilize oocytes during in vitro fertilization. Altogether, post-AI in cattle, sperm and maternal immunity interact differentially depending upon the site of sperm hyperactivation ­ whether it occurs within the uterus or oviduct. Specifically, hyperactivated sperm that enter the uterus after AI or are triggered via sperm-TLR2 activation or other stimuli contribute to sperm-induced uterine inflammation. Such hyperactivated sperm may impede their capacity to ascend to the oviduct. Conversely, sperm that become hyperactivated within the oviduct modulate their interactions with the oviduct and oocytes, which is pivotal during fertilization process. Indeed, the location and timing of sperm hyperactivation partially via TLR2 activation are critical determinants of their different influence on fertility.(AU)

Resumo

Nos últimos quinze anos, a equideocultura foi uma atividade em destaque com significativo crescimento no Brasil e no mundo. O Brasil é o segundo país no mundo que mais utiliza transporte de sêmen equino, ficando atrás apenas dos Estados Unidos e a utilização do sêmen congelado no país vem expandido a cada dia. O índice de prenhez por ciclo, com sêmen equino congelado é variável e oscila entre 25 e 40%. Adicionalmente, sabe-se que o sêmen de alguns garanhões apresenta baixa viabilidade após o descongelamento. A primeira prenhez obtida com sêmen equino congelado foi relatada há cinco décadas. Segundo Cazalez, 2020, é muito difícil recomendar uma dose inseminante padrão para sêmen congelado em equinos. A maioria dos estudos científicos não consegue controlar o efeito de outros fatores "de confusão" como método de processo, fator égua, fator garanhão, técnica de inseminação etc., tornando difícil uma comparação crítica dos mesmos. Rigby et al. (2001) obtiveram taxas de prenhez similares ao se comparar a inseminação artificial profunda em corno uterino com endoscópio e pipeta flexível.(AU)

In the last fifteen years, equine breeding has been a prominent activity with significant growth in Brazil and in the world. Brazil is the second country in the world that most uses equine semen transport, second only to the United States, and the use of frozen semen in the country is expanding every day. The pregnancy rate per cycle with frozen equine semen is variable and ranges from 25 to 40%. Additionally, it is known that the semen of some stallions has low viability after thawing. The first pregnancy obtained with frozen equine semen was reported five decades ago. According to Cazalez, 2020, it is very difficult to recommend a standard insemination dose for frozen semen in horses. Most scientific studies cannot control for the effect of other "confounding" factors such as processing method, mare factor, stallion factor, insemination technique, etc., making it difficult to critically compare them. Rigby et al. (2001) obtained similar pregnancy rates when comparing deep artificial insemination in the uterine horn with an endoscope and flexible pipette.(AU)

Resumo

Ao preservar o espermatozoide suíno no estado líquido ou criopreservado, os componentes do plasma seminal (PS) contidos nos ejaculados podem alterar a capacidade de fertilização desses gametas. O PS contém substâncias essenciais para a manutenção da viabilidade e fertilidade dos espermatozoides. No entanto, esses componentes podem ser deletérios dependendo da quantidade ou duração do tempo de contato entre a ejaculação e a remoção do PS durante o processamento do sêmen para a conservação na forma refrigerada ou congelada. Foram identificadas substâncias que prejudicam (principal proteína plasmática seminal PSPI) ou melhoram (espermadesina PSP-I) a capacidade de fertilização dos espermatozoides. Dependendo dos cachaços e dos procedimentos de colheita de sêmen, a remoção do PS pode ser benéfica antes da preservação no estado líquido ou criopreservado. Em alguns casos, o PS removido antes da congelação pode ser adicionado de volta ao diluente de descongelamento, com efeitos positivos no sêmen descongelado e na viabilidade do espermatozoide no trato reprodutivo da porca. Neste texto, há um foco nos diferentes efeitos de PS em amostras de sêmen refrigerado e criopreservado de suínos com ênfase em como PS modula a função e morfologia das células espermáticas antes, durante e após a preservação de forma refrigerada ou criopreservada.(AU)

When preserving sperm in the liquid or cryopreserved state, seminal plasma (SP) components within ejaculates can alter fertilizing capacity of these gametes. The SP contains substances essential for maintenance of sperm viability and fertility; however, these components can be deleterious depending on quantity, or duration of time before there is removal of SP from sperm in semen processing. Substances that impair (Major seminal plasma protein PSPI - boar) or improve (e.g., spermadhesin PSP-I - boar) sper- matozoa fertilizing capacity have been identified. Depending on individual males and semen collection procedures, SP removal may be beneficial before preservation in the liquid or cryopreserved state. In some cases, SP that is removed can be added back to thawing extender with there being positive effects in thawed sperm and for sperm viability in the female reproductive tract. In this review article, there is a focus on different effects of SP in samples of cooled and cryopreserved semen from boar with there being emphasis on how SP modulates the function and morphology of sperm cells before, during, and after preservation in the refrigerated or cryopreserved state.(AU)

Resumo

The heating rate used during semen thawing plays an important role in reducing structural and functional damage to spermatozoa. In this study, we evaluated the influence of thawing temperature on semen quality, reactive oxygen species (ROS) production, and mitochondrial activity of cryopreserved bovine semen. A total of 195 straws of 0.5 mL from five Holstein Friesian bulls were used (39 straws per bull). Samples underwent 8 to 22 years of storage; they were processed under a standard protocol with tris-egg yolk and stored in liquid nitrogen. Samples were thawed for 30 seconds in a water bath at T1: 36 °C, T2: 38 °C or T3: 40 °C. Sperm motility and kinematics, morphology, structural membrane integrity (SMI), functional membrane integrity (FMI), acrosome integrity (AI), ROS, and mitochondrial membrane potential (ΔΨM) of post-thawing bovine sperm were evaluated. Generalized linear models were fitted to the data. Each model included the effects of bull, storage time, and treatment. The Shapiro-Wilk test was used to assess data normality, and means were compared using the Tukey test. T2 and T3 showed better results for sperm motility and kinematic parameters, SMI (%) (T1 41.9 ± 2.3; T2 45.7 ± 1.9; T3 47.4 ± 2.8), ROS (RFU/min) (T1 0.026 ± 0.007; T2 0.032 ± 0.001; T3 0.031 ± 0.001) and high-ΔΨM (RFU x 103) (67.1± 0,4; 71.3 ± 0.4; 74.2 ± 0.4) (P < 0.05). However, T1 had higher FMI (39.3 ± 2.3) than T2 (34.0 ± 1.9) (P < 0.05), though not significantly (P > 0.05) different from T3 (38.4 ± 2.2). Thawing temperatures of 38 °C and 40 °C increases motility, kinetics, membrane integrity, mitochondrial activity and ROS of cryopreserved bovine semen, compared with more conventional thawing at 36 °C.

A taxa de aquecimento usada durante o descongelamento do sêmen desempenha um papel importante na redução dos danos estruturais e funcionais nos espermatozóides. O objetivo desta pesquisa foi avaliar a influência da temperatura de descongelamento na qualidade do sêmen, produção de espécies reativas de oxigênio (ROS) e atividade mitocondrial do sêmen bovino criopreservado. Foram utilizados 195 palhetas de 0,5 mL de cinco touros Holstein Friesian (39 palhetas por touro). As amostras passaram por oito a 22 anos de armazenamento e foram processadas sob protocolo padrão com Tris-gema de ovo e armazenadas em nitrogênio líquido. As temperaturas de descongelamento foram T1: 36 °C, T2: 38 °C, T3: 40 °C, cada uma por 30 segundos em banho-maria. Pós-descongelamento, a motilidade e cinética dos espermatozoides, morfologia, integridade estrutural da membrana (SMI), integridade funcional da membrana (FMI), integridade acrossomal (AI), ROS e potencial de membrana mitocondrial (ΔΨM) foram avaliados. Modelos lineares generalizados foram ajustados. Cada modelo incluiu os efeitos de touro, tempo de armazenamento e tratamento. A normalidade dos dados foi avaliada pelo teste de Shapiro-Wilk e as médias comparadas pelo teste de Tukey. T2 e T3 apresentaram resultados mais elevados para a maioria dos parâmetros de motilidade e cinemática espermática, SMI (%) (T1 41,9 ± 2,3; T2 45,7 ± 1,9; T3 47,4 ± 2,8), ROS (RFU/min) (T1 0,026 ± 0,007; T2 0,032 ± 0,001; T3 0,031 ± 0,001) e alto ΔΨM (RFU x 103) (67,1 ± 0,4; 71,3 ± 0,4; 74,2 ± 0,4) (P < 0,05). No entanto, T1 apresentou maior FMI (%) (39,3 ± 2,3) em comparação a T2 (34,0 ± 1,9) (P < 0,05), mas não foi diferente do T3 (38,4 ± 2,2) (P > 0,05). Conclui-se que as temperaturas de descongelamento de 38 °C e 40 °C produzem um aumento na motilidade, cinética, integridade de membrana, atividade mitocondrial e ROS do sêmen bovino criopreservado, em comparação com o uso mais convencional de uma temperatura de descongelamento de 36 °C.

Resumo

Spermatozoa experience oxidative, osmotic, chemical, and thermal stresses when cooled, which degrade the quality and fertilizing capacity of the cells. Adding antioxidants to the sperm extender mitigates these alterations. This study evaluated the effect of isoespintanol (ISO) on boar semen subjected to cooling. Fifteen ejaculates from five boars (Susscrofadomestica) were extended in Beltsville thawing solution (BTS) supplemented with 0 µM (control), 5 µM (ISO5), 10 µM (ISO10), 15 µM (ISO15), 20 µM (ISO20), 25 µM (ISO25), and 30 µM (ISO30) of ISO, which were then cooled for five days at 16 °C. Sperm kinetics, total motility (TM), and progressive motility (PM) were evaluated every 24 h using an IVOS computer-assisted sperm analysis (CASA) system. On day 1 and day 5 of cooling, a hypoosmotic test, spectrofluorometry, and flow cytometry were performed to evaluate the following: membrane functionality, measured as a function of hypoosmotic swelling (HOS); total antioxidant capacity (TAC); reactive oxygen species (ROS); and mitochondrial membrane potential (Δ¥M). Regression analysis and comparison of means using the Duncan test were performed. The ISO added had a slight impact on sperm motility, as evidenced by a reduction in TM at 24 h of cooling (but not prior) with the addition of 20 µM of ISO. Similarly, no effect of the ISO on the kinetics and functional integrity of the sperm membrane was observed at 96 h of cooling; however, the regression coefficients indicated that the ISO lowered the rate of decrease in sperm motility and the proportion of rapid spermatozoa relative to the concentration of ISO used. The ISO did not affect the TAC of the cooled semen; however, different concentrations of ISO lowered ROS production in the semen after 96 h of cooling. ISO also impacted the Δ¥M of the spermatozoa at 0 h of cooling, increasing the proportion of low Δ¥M cells and decreasing the proportion of high Δ¥M cells. In conclusion, ISO can reduce the loss of quality and oxidative stress occurring in boar semen during cooling and can modulate the mitochondrial activity of sperm.

Durante a refrigeração, os espermatozoides sofrem estresse oxidativo, osmótico, químico e térmico, que diminuem sua qualidade e afetam sua capacidade de fertilização. A adição de antioxidantes ao diluente espermático é uma alternativa para mitigar essas alterações. O objetivo desta pesquisa foi avaliar o efeito do isospintanol (ISO) na refrigeração do sêmen suíno. Quinze ejaculados de cinco varrascos (Sus scrofa domestica) foram diluídos em BTS suplementado com ISO a 0 (controle), 5 (ISO5), 10 (ISO10), 15 (ISO15), 20 (ISO20), 25 (ISO25) e 30 (ISO30) µM e foram refrigerados por cinco dias a 16 °C. A motilidade total (MT), motilidade progressiva (MP) e cinética dos espermatozóides foram avaliadas a cada 24 h com um sistema CASA IVOS. Nos dias um e cinco de refrigeração, foram avaliadas a funcionalidade da membrana, a capacidade antioxidante total (CAT), as espécies reativas de oxigênio (ROS) e o potencial de membrana mitocondrial (Δ¥M), através do teste hiposmótico (HOS), espectrofluorimetría e citometria de fluxo. Foram realizadas análises de regressão e comparação de médias, pelo teste de Duncan. A adição de ISO teve pouca influência na motilidade espermática, apresentando apenas redução na MT em 24 h de refrigeração, devido à adição de 20 µM. Da mesma forma, não foi observada influência de ISO na cinética e integridade funcional da membrana em 96 horas de refrigeração; porém, os coeficientes de regressão mostraram que ISO produziu menor taxa de diminuição da motilidade e proporção de espermatozoides rápidos dependendo da concentração utilizada. ISO não influenciou significativamente na CAT do sêmen refrigerado; entretanto, diferentes concentrações de ISO reduziram a produção de EROs a partir do sêmen após de 96 h de refrigeração. ISO também influenciou o Δ¥M dos espermatozóides em 0 h de refrigeração, com aumento das células de baixo Δ¥M e diminuição das células de alto Δ¥M. Em conclusão, o isospintanol pode reduzir a perda da qualidade e o estresse oxidativo do sêmen suíno durante a refrigeração e pode modular a atividade mitocondrial do esperma.

Resumo

Up to now, the definitive conclusion of the positive effects of rapid transient thawing at higher temperatures for shorter durations has not been obtained yet and is still under discussion due to some contradictory findings and limited assessment of post-thawed parameters. The purpose of the current study was to evaluate the effectiveness of rapid thawing in water at 70 °C by using various post-thawed parameters of frozen bull spermatozoa. Experiment 1, monitoring the change of temperature inside frozen bull straw thawed in water at different temperatures. Experiment 2, evaluation of various post-thawed characteristics of frozen bull spermatozoa thawed in water at different temperatures by using a computer-assisted sperm analysis, flow cytometry and immunocytochemistry. The time it took for the temperature inside the straw to warm up to 15 °C was nearly twice as faster when the straw was thawed in 70 °C water compared with 39 °C. Although there were differences among bulls, viability, motility, and mitochondrial membrane potential of spermatozoa thawed at 70 °C for 8 seconds and stabilized at 39 °C for 52 seconds were significantly higher than those of controls (thawed at 39 °C for 60 seconds) at 0 and 3 h after thawing. Just after thawing, however, there were no differences in acrosome integrity and distribution of phospholipase C zeta1, whereas mitochondrial reactive oxygen species production was significantly lower in spermatozoa thawed at 70 °C. From these results, we conclude that rapid thawing at 70 °C and then stabilization at 39 °C significantly improves viability, motility and mitochondrial health of bull spermatozoa rather than conventional thawing at 39 °C. The beneficial effect of rapid transient thawing could be due to shorter exposure to temperatures outside the physiological range, consequently maintaining mitochondrial health.(AU)

Resumo

Devido a contaminação bacteriana, utiliza-se antibióticos nos diluentes de sêmen para inibir o crescimento bacteriano durante a sua estocagem. Assim, este trabalho teve por objetivo determinar o limite de toxicidade de diferentes concentrações antibióticas da penicilina/estreptomicina adicionadas ao meio diluente do sêmen e investigar a influência sobre a motilidade espermática. Para isso, o sêmen de cinco reprodutores híbridos comerciais foi coletado uma vez por semana, durante nove semanas, através da técnica da mão enluvada. Cada ejaculado foi distribuído de forma igual entre todos os tratamentos, que consistiram em diferentes concentrações de solução de antibióticos, sendo: T1 = 0,0g/L (controle); T2 = 4,2g/L; e T3 = 12,6g/L. O sêmen diluído em água de coco em pó (ACP-103@) foi conservado por cinco dias e analisado nos dias: D0 (dia da coleta), D2 e D4 (último dia de conservação) quanto ao vigor e à motilidade espermática. Em D0, o sêmen conservado em diluente acrescido de 12,6g de solução antibiótica apresentou menor valor de vigor espermático em relação aos demais tratamentos (p<0,05). Já em D2 e D4, os tratamentos contendo antibióticos apresentaram resultados de vigor aquém dos obtidos no grupo controle (p<0,05). Em relação à motilidade espermática, os maiores percentuais de células móveis foram observados nas amostras de sêmen conservadas em ACP 0,0g/L (controle) quando comparados aos demais tratamentos (p<0,05). Conclui-se que as concentrações antibióticas utilizadas no estudo (4,2 e 12,6 g/L) mostraram efeitos tóxicos logo após a diluição do sêmen suíno, afetando de forma negativa parâmetros seminais durante a conservação a 17 °C.

Due to bacterial contamination, antibiotics are used in semen extenders to inhibit bacterial growth during storage. Thus, the present study aimed to determine the toxicity limit of different antibiotic concentrations of penicillin/streptomycin added to the semen extender and investigate the influence on sperm motility. For this purpose, semen from five commercial hybrid breeders was collected once a week for 9 weeks, using the gloved hand technique. Each ejaculate was distributed equally among all treatments, which consisted of different concentrations of antibiotic solution: T1 = 0.0g/L (control); T2 = 4.2g/L; T3 = 12.6g/L. The semen diluted in powdered coconut water (ACP-103@) was kept for 5 days and analyzed on the following days: D0 (collection day), D2, and D4 (last conservation day) for sperm vigor and motility. In D0, the semen preserved in the diluent added with 12.6 g of antibiotic solution showed a lower sperm vigor value compared to the other treatments (p<0.05). In D2 and D4, treatments containing antibiotics presented vigor results below those obtained in the control group (p<0.05). Regarding sperm motility, higher percentages of mobile cells were observed in semen samples conserved in ACP 0.0 g/L (control) when compared to the other treatments (p<0.05). It is concluded that the antibiotic concentrations used in the study (4.2 and 12.6 g/L) showed toxic effects soon after the swine semen, negatively affecting seminal parameters during storage at 17 °C.

Resumo

The cryopreservation reduces ram sperm quality, decreasing the pregnancy rate of ewes inseminated with thawed sperm. Hence, we aimed to improve the post-thaw quality of ram sperm replacing egg yolk on Tris-Glucose extender with different concentrations of LDL (2 or 8%), associated with the addition of 10 mM non-enzymatic antioxidants (ascorbic acid, hydroxytoluene butylate, ascorbyl palmitate, and trehalose). Semen samples were collected from six rams, split into different treatments, and frozen. After thawing, kinematic (CASA), structural (propidium iodide and carboxyfluorescein diacetate) and functional (hypoosmotic test) sperm membrane integrity was assessed. Total motility, VCL, and LIN were also assessed in thawed samples during 3 h of incubation (38 °C). The results showed that hydroxytoluene butylate at 10 mM in Tris-Glucose extender with 8% LDL improved velocity parameters immediately post-thaw compared with Tris-Glucose egg yolk extender, as well as prevented the reduction of total motility and VCL after incubation. There was no benefit of adding ascorbic acid and trehalose. Moreover, for the first time, it was shown the motility impairment promoted by ascorbyl palmitate to ram sperm.(AU)

Resumo

Objetivou-se com este trabalho avaliar a viabilidade seminal de coelhos após refrigeração a 5°C utilizando três diluentes comerciais, indicados para refrigeração de sêmen de outras espécies monogástricas. Foram realizadas dez colheitas de sêmen de cada reprodutor. Os ejaculados de cada coelho eram misturados, obtendo-se um pool de sêmen. Em seguida, o pool heterospérmico foi dividido em três tratamentos, de acordo com o diluente utilizado: BotuDogⓇ (cães); BotuSemen® (equinos); e Beltsville Thawing Solution - BTS (suínos). As amostras foram avaliadas quanto aos parâmetros macroscópicos, microscópicos e funcionais em quatro momentos: sêmen fresco (0 h) e refrigerado (16, 24 e 48 h). Os valores médios de motilidade, vigor e defeitos totais do sêmen fresco foram de 86,0%, 3,05 e 11,5%, respectivamente. Após o início do resfriamento, observou-se comportamento linear decrescente para a motilidade e vigor espermático do sêmen em função do tempo, diferindo (P < 0,05) entre os tratamentos. Destaca-se que o tratamento diluído em BTS apresentou redução na manutenção dos parâmetros avaliados de forma mais pronunciada (P < 0.05) ao longo do tempo, apresentando os menores valores para motilidade e vigor espermático dentro de cada tempo avaliado: 16h [20,6 ± 7,28 e 0,75 (0,375 1,5)], 24h [12,0 ± 6,80 e 0 (0 - 1,0)] e 48h [3,0 ± 2,13 e 0 (0 - 0,125)]. Após 48 h de resfriamento, o BotuDogⓇ foi o que apresentou maior valor para motilidade espermática (71,0 ± 2,08) e, juntamente, com o BotuSemenⓇ apresentaram maior valor para vigor espermático (2,5). De acordo com os dados obtidos os diluentes BotuDogⓇ e BotuSemenⓇ mostraram-se eficientes em manter parâmetros espermáticos adequados, apresentando boa viabilidade espermática em até 48h pós refrigeração a 5°C. Foram obtidos, resultados inéditos quanto a parâmetros espermáticos do sêmen de coelho refrigerado que podem ser utilizados como valores de referência para o manejo reprodutivo e processamento do semen desses animais, visto a inexistênca dessas recomendações técnicas.

The objective of this work was to evaluate the seminal viability of rabbits after refrigeration at 5°C using three commercial diluents, indicated for refrigeration of semen from other monogastric species. Ten semen collections were performed from each breeder. The ejaculates of each rabbit were mixed, obtaining a pool of semen. Then, the heterospermic pool was divided into three treatments, according to the diluent used: BotuDog (dogs); BotuSemenⓇ (horses); and Beltsville Thawing Solution - BTS (pigs). The samples were evaluated for macroscopic, microscopic, and functional parameters in four moments: fresh (0 h) and refrigerated (16, 24, and 48 h) semen. The average values of motility, vigor, and total defects of fresh semen were 86.0%, 3.05 and 11.5%, respectively. After the beginning of cooling, a decreasing linear behavior was observed for motility and sperm vigor of semen as a function of time, differing (P < 0.05) between treatments. It is noteworthy that the treatment diluted in BTS® showed a more pronounced reduction in the maintenance of the evaluated parameters (P < 0.05) over time, with the lowest values for sperm motility and vigor within each evaluated time: 16h [20.6 +7.28 and 0.75 (0.375 - 1.5)], 24h [12.0± 6.80 and 0 (0 - 1.0)] and 48h [3.0±2.13 and 0 (0 - 0.125)]. After 48 h of cooling, BotuDog presented the highest value for sperm motility (71.0 ± 2.08) and, together with BotuSemenⓇ, presented the highest value for sperm vigor (2.5). According to the data obtained, BotuDog and BotuSemenⓇ diluents were efficient in maintaining adequate sperm parameters, showing good sperm viability in up to 48 hours after refrigeration at 5°C. Through this work, unpublished results were obtained regarding spermatic parameters of refrigerated rabbit semen that can be used as reference values for reproductive management and semen processing of these animals, given the lack of these technical recommendations.

El objetivo de este trabajo fue evaluar la viabilidad seminal de conejos después de refrigeración a 5°C utilizando tres diluyentes comerciales, indicados para la refrigeración de semen de otras especies monogástricas. Se realizaron diez colectas de semen de cada reproductora. Se mezclaron los eyaculados de cada conejo, obteniendo un pool de semen. Luego, el pool heterospérmico se dividió en tres tratamientos, según el diluyente utilizado: BotuDogⓇ (perros); BotuSemenⓇ (caballos); y Beltsville Thawing Solution - BTS® (cerdos). Las muestras fueron evaluadas para parámetros macroscópicos, microscópicos y funcionales en cuatro momentos: semen fresco (0 h) y refrigerado (16, 24 y 48 h). Los valores promedio de motilidad, vigor y defectos totales del semen fresco fueron 86,0%, 3,05 y 11,5%, respectivamente. Después del inicio del enfriamiento, se observó un comportamiento lineal decreciente para la motilidad y el vigor espermático del semen en función del tiempo, difiriendo (P < 0.05) entre tratamientos. Cabe destacar que el tratamiento diluido en BTS® mostró una reducción más pronunciada en el mantenimiento de los parámetros evaluados (P<0,05) a lo largo del tiempo, con los valores más bajos de motilidad espermática y vigor dentro de cada tiempo evaluado: 16h [20,6 ± 7,28 y 0,75 (0,375 -1.5)], 24h [12,0 ± 6,80 y 0 (0 - 1,0)] y 48h [3,0±2,13 y 0 (0 - 0,125)]. Después de 48 h de enfriamiento, BotuDogⓇ presentó el valor más alto de motilidad espermática (71,0 +2,08) y, junto con BotuSemenⓇ, presentó el valor más alto de vigor espermático (2,5). De acuerdo con los datos obtenidos, los diluyentes BotuDogⓇ y BotuSemenⓇ fueron eficientes en mantener parámetros espermáticos adecuados, mostrando buena viabilidad espermática hasta 48 horas después de la refrigeración a 5°C. A través de este trabajo se obtuvieron resultados inéditos respecto a parámetros espermáticos de semen de conejo refrigerado que pueden ser utilizados como valores de referencia para el manejo reproductivo y procesamiento de semen de estos animales, dada la falta de estas recomendaciones técnicas.

Resumo

This study aimed to develop a protocol for the cryopreservation of Pseudoplatystoma corruscans semen. For this, mature males were hormonally induced with a single dose of carp pituitary extract (5 mg/kg body weight). Semen was collected and evaluated. Two cryoprotectants were tested to compose the diluents: dimethyl acetamide (DMA) and dimethyl sulfoxide (Me2SO), in two concentrations (8% and 10%), + 5.0% glucose + 10% egg yolk. The semen was diluted in a 1: 4 ratio (semen: extender), packed in 0.5 mL straws and frozen in a dry shipper container in liquid nitrogen vapors. After thawing, sperm kinetics, sperm morphology and DNA integrity of cryopreserved sperm were evaluated. Pseudoplatystoma corruscans males produced semen with sperm motility > 80%. After thawing, all treatments provided semen with total sperm motility > 40%, with no significant difference (P < 0.05) between them, as well as between the other sperm kinetic parameters evaluated. The treatments with DMA provided a smaller fragmentation of the DNA of the gametes. Sperm malformations were identified in both fresh and cryopreserved semen, with a slight increase in these malformations being identified in sperm from thawed P. corruscans semen samples.(AU)

Este estudo teve como objetivo desenvolver um protocolo para a criopreservação do sêmen de Pseudoplatystoma corruscans. Para tal, machos maduros foram induzidos hormonalmente com uma dose única de extrato de hipófise de carpa (5 mg/kg de peso vivo). O sêmen foi coletado e avaliado. Sendo testados para compor os diluentes, dois crioprotetores: dimetil acetamida (DMA) e dimetil sulfóxido (Me2SO), em duas concentrações (8% e 10%), + 5,0% glicose + 10% gema de ovo. O sêmen foi diluído na proporção 1: 4 (sêmen: extensor), embalado em palhetas de 0,5 mL e congelado em container dryshipper em vapores de nitrogênio líquido. Após o descongelamento, foram avaliados os aspectos cinéticos espermáticos, a morfologia espermática e a integridade do DNA dos espermatozoides criopreservados. Os machos de P. corruscans produziram sêmen com motilidade espermática > 80%. Todos os tratamentos proporcionaram após o descongelamento sêmen com motilidade espermática total > 40%, sem diferença significativa (P < 0,05) entre eles, como também entre os demais parâmetros cinéticos espermáticos avaliados. Os tratamentos com DMA proporcionaram uma menor fragmentação do DNA dos gametas. Malformações espermáticas foram identificadas, tanto no sêmen fresco, como no criopreservado, sendo identificado um aumento discreto dessas malformações nos espermatozoides das amostras de sêmen descongeladas de P. corruscans.(AU)

Resumo

A inseminação artificial em cadelas contribui para o melhoramento genético da espécie, previne algumas doenças sexualmente transmissíveis a partir da cópula e possibilita a reprodução de animais que não poderiam copular de forma natural, seja por motivos anatômicos, geográficos ou comportamentais. Todavia, nem sempre é possível utilizar o sêmen fresco, sendo assim necessário um diluente para resfriar e mantê-lo viável por determinado período. Diante disso, o objetivo com este trabalho foi analisar o sêmen canino diluído em água de coco e refrigerado, à 5 ºC em diferentes tempos. Foram utilizados cinco cães da raça Hounds do Brasil, realizando três colheitas de sêmen de cada animal, com intervalos de sete dias. Os ejaculados foram mantidos a temperatura de 37ºC e realizado análises macroscópicas (volume, cor, aspecto e odor) e microscópicas (motilidade, vigor, concentração e morfologia espermática). Em seguida, os ejaculados foram diluídos em água de coco natural a uma concentração de 200 milhões de espermatozoides/mL, e mantidos à temperatura de 5 °C, por até 72 horas. Nos intervalos de seis, doze, vinte e quatro, trinta e seis, quarenta e oito, e setenta e duas horas, as amostras foram avaliadas quanto a motilidade e vigor espermático. Os ejaculados frescos apresentaram em média volume de 6,2 mL, cor branca, aspecto aquoso a leitoso, odor "sui generis", motilidade espermática de 89,5 %, vigor espermático 4,3, concentração média de 418 x106espermatozoides/mL e 7,3% de alterações patológicas. Após o início do resfriamento à 5 ºC, os valores de motilidade e vigor diminuíram com o passar do tempo, sendo os menores valores encontrados após 48 e 72 horas. O diluente a água de coco in natura mostrou-se eficiente para refrigeração de sêmen canino, à 5 ºC, conservando-o por um período de até 36h após a colheita, conforme preconizado pelo Colégio Brasileiro de Reprodução Animal.(AU)

improvement of the species, prevents some sexually transmitted diseases through copulation and allows the reproduction of animals that could not copulate naturally, either for anatomical, geographic or behavioral reasons. However, it is not always possible to use fresh semen, thus requiring a diluent to cool and keep it viable for a certain period. Therefore, the objective of this work was to analyze canine semen diluted in coconut water and refrigerated at 5 ºC at different times. Five Brazilian Hounds were used, performing three semen collections from each animal, with intervals of seven days. The ejaculates were kept at a temperature of 37 ºC and macroscopic (volume, color, appearance and odor) and microscopic (motility, vigor, concentration and sperm morphology) analyzes were performed. Then, the ejaculates were diluted in natural coconut water at a concentration of 200 million sperm/mL, and kept at a temperature of 5 °C for up to 72 hours. At intervals of six, twelve, twenty-four, thirty-six, forty-eight, and seventy-two hours, samples were evaluated for sperm motility and vigor. Fresh ejaculates had an average volume of 6.2 mL, white color, watery to milky appearance, "sui generis" odor, 89.5% sperm motility, 4.3 sperm vigor, average concentration of 418 x106 spermatozoa/mL and 7.3%pathological changes. After the beginning of cooling at 5 °C, the values of motility and vigor decreased over time, with the lowest values found after 48 and 72 hours. The in natura coconut water extender proved to be efficient for cooling canine semen at5 ºC, keeping it for a period of up to 36 hours after harvest, as recommended by the Brazilian College of Animal Reproduction.(AU)

Artificial insemination in bitches contributes to the genetic La inseminación artificial en perras contribuye a la mejora genética de la especie, previene algunas enfermedades de transmisión sexual a través de la cópula y permite la reproducción de animales que no podrían copular de forma natural, ya sea por razones anatómicas, geográficas o de comportamiento. Sin embargo, no siempre es posible utilizar semen fresco, por lo que se requiere un diluyente para enfriarlo y mantenerlo viable durante un cierto período. Por tanto, el objetivo de este trabajo fue analizar semen canino diluido en agua de coco y refrigerado a 5 ºC en diferentes tiempos. Se utilizaron cinco sabuesos brasileños, realizándose tres colectas de semen de cada animal, con intervalos de siete días. Los eyaculados se mantuvieron a una temperatura de 37 ºC y se realizaron análisis macroscópicos (volumen, color, apariencia y olor) y microscópicos (motilidad, vigor, concentración y morfología espermática). Luego, los eyaculados se diluyeron en agua de coco natural a una concentración de 200 millones de espermatozoides/mL y se mantuvieron a una temperatura de 5 °C hasta por 72 horas. A intervalos de seis, doce, veinticuatro, treinta y seis, cuarenta y ocho y setenta y dos horas, se evaluó la motilidad y el vigor de los espermatozoides en las muestras. Los eyaculados frescos tuvieron un volumen promedio de 6,2 mL, color blanco, apariencia acuosa a lechosa, olor "sui generis", motilidad espermática de 89,5%, vigor espermático de 4,3, concentración promedio de 418 x106 espermatozoides/mL y cambios patológicos de 7,3%. Después del inicio del enfriamiento a 5 °C, los valores de motilidad y vigor disminuyeron con el tiempo, encontrándose los valores más bajos a las 48 y 72 horas. El diluyente de agua de coco in natura demostró ser eficaz para enfriar el semen canino a5 ºC, manteniéndolo por un período de hasta 36 horas después de la cosecha, según lo recomendado por el Colegio Brasileño de Reproducción Animal.(AU)