Validation of the CellRox Deep Red ® fluorescent probe to oxidative stress assessment in equine spermatozoa

Considering the importance of ROS influence on sperm functionality and some limitations in sperm oxidative stress assessment methods, a field to studies of new techniques are still open. In this sense, the aim of this study is to validate the ROS detection technique through the CellRox Deep Red Reagent®probe in stallion sperm. Four stallions were used and the analyses were conducted on four replicates of semen samples from each of stallion (n = 16). The results of the polynomial regression presented a quadratic effect, high determination coefficient value (R2 = 0.88) and high significant P value (P < 0.0001). The CellRox Deep Red® fluorescent probe is able to detect reactive oxygen species in equine sperm, indicating accurately the occurrence of oxidative stress in stallion semen.

Validation of the CellRox Deep Red ® fluorescent probe to oxidative stress assessment in equine spermatozoa

Considering the importance of ROS influence on sperm functionality and some limitations in sperm oxidative stress assessment methods, a field to studies of new techniques are still open. In this sense, the aim of this study is to validate the ROS detection technique through the CellRox Deep Red Reagent®probe in stallion sperm. Four stallions were used and the analyses were conducted on four replicates of semen samples from each of stallion (n = 16). The results of the polynomial regression presented a quadratic effect, high determination coefficient value (R2 = 0.88) and high significant P value (P < 0.0001). The CellRox Deep Red® fluorescent probe is able to detect reactive oxygen species in equine sperm, indicating accurately the occurrence of oxidative stress in stallion semen.(AU)

Caracterização física e estrutural de espermatozoides no ejaculado de Caprinos Azul, Canindé, Moxotó e Repartido / Physical and structural characterization of sperm in the ejaculate from Azul, Caninde, Moxotó and Repartido goat races

This study aimed to evaluate physically and structurally ejaculates from locally adapted goats in therainy season. Semen pool formed by the four goats of each breed was evaluated for physical, diluted in Tris-eggyolk and frozen. After thawing, it was diluted in Tris and incubated with carboxyfluorescein diacetate andpropidium iodide, to evaluate the integrity of the plasma membrane and JC1 to assess mitochondrial activity.The percentage of cells with damaged membrane and mitochondrial activity in spermatozoa between breed werecompared, every hour for three hours. There was no significant difference (P > 0,05) in relation to thepercentage of cells with damaged plasma membrane, as well as between the incubation times. The Azul breedhad lower mitochondrial activity (P < 0,05). The evaluated semen of all breeds showed no significant damage tothe plasma membrane in the rainy season, but the Azul breed had lower mitochondrial activity in sperm cells.(AU)

Análise da integridade de membrana de espermatozoides extraídos de fragmentos frescos de testículos de cães / Sperm membrane integrity analysis from dog fresh testis

To evaluate testicular tissue before cryopreservation is important to quantify and qualify losses ofsperm during the freezing/thawing of testicular tissue. The aim of this study was to analyze the sperm plasmamembrane structural and functional integrity on post-pubertal dogs (n = 7) fresh testis. The sperm fromtesticular tissue were submitted to plasma membrane structural and functional integrity analysis by fluorescentmicroscopy using SYBR 14 and Propidium Iodide and the hiposmotic test, respectively. For statistical analysis,it was used normality test (Shapiro Wilk) and Wilcoxon test (R 3.3.1; P > 0.05). It was observed 94.9% and91.8% spermatozoa presenting structural and functional integrity, respectively. Thus, analysis of the membraneintegrity is an important tool to analyze spermatozoa extracted from testicles. Despite the fluorescence be apractical method, it has a high cost.(AU)

Caracterização física e estrutural de espermatozoides no ejaculado de Caprinos Azul, Canindé, Moxotó e Repartido / Physical and structural characterization of sperm in the ejaculate from Azul, Caninde, Moxotó and Repartido goat races

This study aimed to evaluate physically and structurally ejaculates from locally adapted goats in therainy season. Semen pool formed by the four goats of each breed was evaluated for physical, diluted in Tris-eggyolk and frozen. After thawing, it was diluted in Tris and incubated with carboxyfluorescein diacetate andpropidium iodide, to evaluate the integrity of the plasma membrane and JC1 to assess mitochondrial activity.The percentage of cells with damaged membrane and mitochondrial activity in spermatozoa between breed werecompared, every hour for three hours. There was no significant difference (P > 0,05) in relation to thepercentage of cells with damaged plasma membrane, as well as between the incubation times. The Azul breedhad lower mitochondrial activity (P < 0,05). The evaluated semen of all breeds showed no significant damage tothe plasma membrane in the rainy season, but the Azul breed had lower mitochondrial activity in sperm cells.

Análise da integridade de membrana de espermatozoides extraídos de fragmentos frescos de testículos de cães / Sperm membrane integrity analysis from dog fresh testis

To evaluate testicular tissue before cryopreservation is important to quantify and qualify losses ofsperm during the freezing/thawing of testicular tissue. The aim of this study was to analyze the sperm plasmamembrane structural and functional integrity on post-pubertal dogs (n = 7) fresh testis. The sperm fromtesticular tissue were submitted to plasma membrane structural and functional integrity analysis by fluorescentmicroscopy using SYBR 14 and Propidium Iodide and the hiposmotic test, respectively. For statistical analysis,it was used normality test (Shapiro Wilk) and Wilcoxon test (R 3.3.1; P > 0.05). It was observed 94.9% and91.8% spermatozoa presenting structural and functional integrity, respectively. Thus, analysis of the membraneintegrity is an important tool to analyze spermatozoa extracted from testicles. Despite the fluorescence be apractical method, it has a high cost.