Sperm cryopreservation of Prochilodus brevis using different concentrations of non-permeable cryoprotectants

Abstract The action of substances with non-permeable cryoprotectant potential, besides glucose, has not yet been studied for the species Prochilodus brevis. The objective of this work was to evaluate the action of four non-permeable cryoprotectants on this species sperm cryopreservation. Five pools were cryopreserved in a solution of 5% glucose and 10% dimethyl sulfoxide (Me2SO) associated or not (control) with cryoprotectants egg yolk (5, 10 or 12%), soy lecithin (2.5, 7.5 or 10%), sucrose (5, 10 or 20%) and lactose (5, 8 or 15%). After thawing, samples were evaluated for sperm kinetics (total motility, motility duration, velocities, and wobble - WOB), morphology and membrane and DNA integrity. The treatments containing egg yolk improved significantly (P<0.05) results when compared the control for the membrane integrity parameter. When compared to other treatments, egg yolk, at any concentration, presented higher results (P<0.05) for membrane integrity, total motility, curvilinear velocity (VCL) and average path velocity (VAP) parameters. Egg yolk also showed the best results for WOB, but it did not differ from 5% and 8% lactose and 5% and 20% sucrose. Soy lecithin had the lowest percentages of morphologically normal sperm (P<0.05), while the other treatments did not differ from each other. There was no difference regarding DNA integrity data. Thus, 5% egg yolk is indicated as a non-permeable cryoprotectant for P. brevis, in association with 5% glucose and 10% Me2SO.

Sperm cryopreservation of Prochilodus brevis using different concentrations of non-permeable cryoprotectants

The action of substances with non-permeable cryoprotectant potential, besides glucose, has not yet been studied for the species Prochilodus brevis. The objective of this work was to evaluate the action of four non-permeable cryoprotectants on this species sperm cryopreservation. Five pools were cryopreserved in a solution of 5% glucose and 10% dimethyl sulfoxide (Me2SO) associated or not (control) with cryoprotectants egg yolk (5, 10 or 12%), soy lecithin (2.5, 7.5 or 10%), sucrose (5, 10 or 20%) and lactose (5, 8 or 15%). After thawing, samples were evaluated for sperm kinetics (total motility, motility duration, velocities, and wobble - WOB), morphology and membrane and DNA integrity. The treatments containing egg yolk improved significantly (P<0.05) results when compared the control for the membrane integrity parameter. When compared to other treatments, egg yolk, at any concentration, presented higher results (P<0.05) for membrane integrity, total motility, curvilinear velocity (VCL) and average path velocity (VAP) parameters. Egg yolk also showed the best results for WOB, but it did not differ from 5% and 8% lactose and 5% and 20% sucrose. Soy lecithin had the lowest percentages of morphologically normal sperm (P<0.05), while the other treatments did not differ from each other. There was no difference regarding DNA integrity data. Thus, 5% egg yolk is indicated as a non-permeable cryoprotectant for P. brevis, in association with 5% glucose and 10% Me2SO.(AU)

Supplementation of cryodiluent medium with sulfated polysaccharides from green seaweeds in the freezing of Colossoma macropomum semen / Suplementação do meio criodiluidor com polissacarídeos sulfatados de macroalgas verdes na congelação do sêmen de Colossoma macropomum

This study proposes to investigate the addition of sulfated polysaccharides (SP) extracted from two species of green seaweeds, Ulva lactuca and Caulerpa racemosa, to Colossoma macropomum semen cryodiluent medium. Four concentrations of SP (1.0, 2.0, 3.0, or 4.0 mg mL-1) of each seaweed were evaluated. Semen was collected during the month of September in Fortaleza - CE, Brazil. Fresh semen samples were analyzed for the parameters of total sperm motility, curvilinear velocity (VCL), straight line velocity (VSL), average path velocity (VAP), sperm morphology, membrane integrity, and DNA integrity. Then, the samples were cryopreserved in freezing medium containing 10% dimethyl sulfoxide (DMSO) + 5% glucose, which was supplemented with different concentrations of SP. An unsupplemented treatment was used as control. After 15 days, they were thawed in a water bath at 45 ºC for eight seconds and the same analyses of fresh semen were performed. Statistical analysis revealed that there were no significant differences (p > 0.05) between the different tested concentrations of SP for any of the evaluated parameters. Compared with the control, there was no difference in concentrations (p > 0.05) for total motility; however, for VCL, VSL, and VAP, the U. lactuca concentrations of 3.0 and 4.0 mg mL-1 were detrimental (p < 0.05). The same was observed with 4.0 mg mL-1 of C. racemosa for VSL and VAP. In terms of morphology, 1.0 and 4.0 mg mL-1 of C. racemosa reduced normal sperm (p < 0.05), whereas for the other concentrations there was no difference (p > 0.05). All concentrations of both seaweeds maintained plasma membrane integrity (p > 0.05). As for DNA integrity, only 4.0 mg mL-1 of U. lactuca produced lower results than the control (p < 0.05), whereas the other concentrations maintained the number of spermatozoa with intact DNA (p > 0.05). Based on the results, higher concentrations of SP are harmful to tambaqui sperm in the freezing medium, whereas lower concentrations maintain sperm parameters. Further research is warranted to better investigate the antioxidant potential of these polymers in cryodiluent medium for C. macropomum as well as other fish species.

O estudo teve como objetivo avaliar a adição de polissacarídeos sulfatados (PS) extraídos de duas espécies de macroalgas verdes, Ulva lactuca e Caulerpa racemosa, no meio criodiluidor do sêmen de Colossoma macropomum. Para isso, foram avaliadas quatro concentrações de PS (1,0; 2,0; 3,0 ou 4,0 mg mL-1), de cada macroalga. A coleta de sêmen foi realizada durante o mês de setembro, em Fortaleza, Ceará, Brasil. As amostras de sêmen fresco foram analisadas quanto aos parâmetros de motilidade total dos espermatozoides, velocidade curvilinear (VCL), velocidade em linha reta (VSL), velocidade média do trajeto (VAP), morfologia espermática, integridade de membrana e integridade de DNA. Em seguida, foram criopreservadas em meio de congelação contendo dimetilsulfóxido (DMSO) 10% + glicose 5%, e suplementadas com as diferentes concentrações de PS, tendo ainda um tratamento não suplementado como controle. Após 15 dias, foram descongeladas em banho-maria a 45 ºC por oito segundos, e as mesmas análises do sêmen fresco foram realizadas. Através da análise estatística, os resultados mostraram que não houveram diferenças significativas (p > 0,05) entre as diferentes concentrações de PS testadas para nenhum dos parâmetros avaliados. Já em relação ao controle, não houve diferença nas concentrações (p > 0,05) para a motilidade total, no entanto, para VCL, VSL e VAP, as concentrações de 3,0 e 4,0 mg mL-1 de U. lactuca foram prejudiciais (p < 0,05). O mesmo foi observado em 4,0 mg mL-1 de C. racemosa para VSL e VAP. Para a morfologia, 1,0 e 4,0 mg mL-1 de C. racemosa reduziram os espermatozoides normais (p < 0,05), enquanto para as demais concentrações não houve diferença (p > 0,05). Para todas as concentrações de ambas as macroalgas, a integridade de membrana plasmática foi mantida (p > 0,05). Quanto à integridade do DNA, apenas 4,0 mg mL-1 de U. lactuca foi inferior ao controle (p < 0,05), enquanto as demais concentrações mantiveram o número de espermatozoides com DNA íntegro (p > 0,05). De acordo com os resultados obtidos, concentrações mais elevadas de PS são prejudiciais aos espermatozoides de tambaqui no meio de congelação, enquanto concentrações mais baixas mantiveram parâmetros espermáticos. Estudos posteriores são indicados para melhor avaliar o potencial antioxidante destes polímeros no meio criodiluidor do sêmen de C. macropomum, bem como de outras espécies de peixes.

Determinação e diferenciação sexual em peixes teleósteos: papel dos fatores ambientais e genéticos / Sexual determination and differentiation in teleost fish: the role of environmental and genetic factors

Peixes teleósteos possuem diversas maneiras de determinação e diferenciação sexual. De modo que, fatores genéticos e ambientais podem atuar interagindo para determinar o sexo e agir sobre a diferenciação das gônadas desses animais. Os fatores ambientais atuam de diferentes formas para determinar o sexo de peixe, uma vez que sua ação é dependente da espécie. Fatores como temperatura, pH, densidade populacional e poluição podem causara masculinização ou feminização, agindo principalmente sobre os hormônios sexuais e muitas vezes causando a apoptose ovariana e, consequentemente, promovendo a masculinização. Já a determinação genética se dar por cromossomos sexuais (sistema monogênico) ou por ação autossômica (sistema poligênica). No sistema monogênico já foram observados vários modelos de cromossomos sexuais, sendo os principais XX/XY (machos heterogaméticos) e ZW/ZZ (fêmeas heterogaméticas). Com isso, é possível observar que os peixes teleósteos possuem uma grande diversidade de determinação sexual e diferenciação gonadal.

Teleost fish have various forms of sexual determination and differentiation. Genetic and environmental factors can interact to determine sex and act on the differentiation of the gonads of these animals. Environmental factors act in different ways to determine the sex of the fish, as their action depend on the species. Factors such as temperature, pH, population density and pollution can cause a masculinization or a feminization, by acting on the hormones and, often, the ovarian apoptosis. The genetic determination is given by the sexual chromosome (monogenic system) or by the autosomal action (polygenic system). In the monogenic system several models of sexual chromosomes were observed, the main ones being XX / XY (heterogeneous males) and ZW / ZZ(heterogeneous females). With this, it is possible to observe that teleost possess a great amplitude of sexual determination and gonadal differentiation.

Determinação e diferenciação sexual em peixes teleósteos: papel dos fatores ambientais e genéticos / Sexual determination and differentiation in teleost fish: the role of environmental and genetic factors

Peixes teleósteos possuem diversas maneiras de determinação e diferenciação sexual. De modo que, fatores genéticos e ambientais podem atuar interagindo para determinar o sexo e agir sobre a diferenciação das gônadas desses animais. Os fatores ambientais atuam de diferentes formas para determinar o sexo de peixe, uma vez que sua ação é dependente da espécie. Fatores como temperatura, pH, densidade populacional e poluição podem causara masculinização ou feminização, agindo principalmente sobre os hormônios sexuais e muitas vezes causando a apoptose ovariana e, consequentemente, promovendo a masculinização. Já a determinação genética se dar por cromossomos sexuais (sistema monogênico) ou por ação autossômica (sistema poligênica). No sistema monogênico já foram observados vários modelos de cromossomos sexuais, sendo os principais XX/XY (machos heterogaméticos) e ZW/ZZ (fêmeas heterogaméticas). Com isso, é possível observar que os peixes teleósteos possuem uma grande diversidade de determinação sexual e diferenciação gonadal.(AU)

Teleost fish have various forms of sexual determination and differentiation. Genetic and environmental factors can interact to determine sex and act on the differentiation of the gonads of these animals. Environmental factors act in different ways to determine the sex of the fish, as their action depend on the species. Factors such as temperature, pH, population density and pollution can cause a masculinization or a feminization, by acting on the hormones and, often, the ovarian apoptosis. The genetic determination is given by the sexual chromosome (monogenic system) or by the autosomal action (polygenic system). In the monogenic system several models of sexual chromosomes were observed, the main ones being XX / XY (heterogeneous males) and ZW / ZZ(heterogeneous females). With this, it is possible to observe that teleost possess a great amplitude of sexual determination and gonadal differentiation.(AU)