Ação do extrato etanólico de Mufumbo sobre a criopreservação do sêmen de garanhão / Action of the ethanol extract of Mufumbo on cryopreservation of stallion sêmen

Various natural antioxidants are being added to the freezing diluents in order to minimize deleteriouseffects to the membrane of spermatozoa during the cryopreservation process. Avaliou if stallions semencharacteristics cryopreserved amid thinner Botu-crio plus ethanol extract from the bark of mufumbo(Combretum leprosum) at different concentrations (30 mg, 60 mg and 120 mg). Samples of each treatment weresubmitted to hypoosmotic test membrane integrity tests and mitochondrial function (fluorescent tubes); Therewas no significant difference (P > 0.05) and the percentage of spermatozoa reactive to hiposmotic test betweenthe groups tested. The percentage of sperm with intact plasma membrane, as well as the mitochondrial potentialwere not statistically different (P > 0.05) between the control and treatment.(AU)

Ação do extrato etanólico de Mufumbo sobre a criopreservação do sêmen de garanhão / Action of the ethanol extract of Mufumbo on cryopreservation of stallion sêmen

Various natural antioxidants are being added to the freezing diluents in order to minimize deleteriouseffects to the membrane of spermatozoa during the cryopreservation process. Avaliou if stallions semencharacteristics cryopreserved amid thinner Botu-crio plus ethanol extract from the bark of mufumbo(Combretum leprosum) at different concentrations (30 mg, 60 mg and 120 mg). Samples of each treatment weresubmitted to hypoosmotic test membrane integrity tests and mitochondrial function (fluorescent tubes); Therewas no significant difference (P > 0.05) and the percentage of spermatozoa reactive to hiposmotic test betweenthe groups tested. The percentage of sperm with intact plasma membrane, as well as the mitochondrial potentialwere not statistically different (P > 0.05) between the control and treatment.

Efeito da somatotropina bovina recombinante (rbST) sobre a concentração espermática de ovinos Santa Inês / Effect of recombinant bovine somatotropin (rbST) in sperm concentration of sheep Santa Inês

This study aimed to evaluate among the seminal characteristics, sperm concentration of Santa Inessheep, aged 22-36 months treated with recombinant bovine somatotropin (rbST). Divided into groups randomly:GI (2mL / 0.9% NaCl), G-II (100mg / rbST) and G-III (125mg / rbST), receiving treatments subcutaneouslyevery 14 days (D0,14,28, 42,56,70). They were measured scrototesticular biometrics. The ejaculates werecollected by artificial vagina, with dummy sheep, and analyzed for volume, vortex, motility, vigor, morphologyand sperm concentration. There was no significant difference (P > 0.05) in PE (30,1cm) and in almost all semenparameters. However, on sperm concentration (sperm / mL) in G-III, there was an increase (787.69 ± 480.72)compared to groups. It was concluded that the dose of 125mg / rbST increases the sperm concentration of ovineSanta Ines.(AU)

Efeito da melatonina sobre a integridade das membranas plasmática e mitocondrial de espermatozoides criopreservados de ovino / Effect of Melatonin on the plasmatic and mitochondrial integrity membrane of sperm cryopreserved ram

This study evaluate the effect of melatonin supplementation to TRIS-GEMA diluter in plasmatic andmitochondria membrane integrity of semen ram cryopreserved. Was used seven ejaculates of six ram,whichwere pooled in pool, according to the experimental groups: Control; T1 - 1x10-7 mol / L and T2 - 1x10-9 mol / Lmelatonin. Posteriorly the diluting the samples were packaged in straws of 0.25 ml and cryopreserved. Afterthawing at 37°C for 30 seconds, the samples were analyzed for Test thermoresistance slow (TTR) andacrosomal membrane integrity. For statistical analysis we used the Duncan test (α = 0.05) for meancomparison. Treatments 1 and 2 differed statistically control for plasma membrane integrity at times 60, 120and 180min. It was concluded that supplementation 1x10-7mol / L and 1x10-9mol / L of melatonin increased theintegrity of the plasma membrane to 60,120 and 180 minutes.(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)

Efeito da Somatrotopina Bovina Recombinante (rbST) associado a um protocolo de Inseminação Artificial em Tempo Fixo em cabras SPRD / Effect of Recombinant Bovine Somatotropin (rbST) associated with a protocol Artificial Insemination in Fixed Time in SPRD goats

We evaluated the effect of Recombinant Bovine Somatotropin (rbST) seven days before the start of thesynchronization protocol on pregnancy rate in goats. Were used 101 females without defined breed in semiintensivesystem, randomly divided into two groups. Seven days before the start of estrus synchronization, G1 (n= 49) received 125 mg of rbST, IM, and G2 (n = 52) physiological saline, subcutaneously. In D0, the groupsreceived 1 mL of BE, IM, and were synchronized with intravaginal sponges impregnated with 60 mg ofmedroxyprogesterone for 11 days. In D9, they received 300 IU of eCG and 75 µg of PGF2α. On D11, thesponges were removed, we performed IATF 36 and 48 hours later, transcervically. It was used pool of AngloNubians semen. Gestational diagnosis was performed 30 days later. A single dose administration of rbST, sevendays before estrus synchronization, did not increase the pregnancy rate.(AU)

Efeito da melatonina sobre a viabilidade de espermatozóides criopreservados de ovinos / Effect of melatonin on the feasibility of sperm cryopreserved of ram

This study to evaluate the effect of melatonin supplementation to TRIS-GEMA diluter in sperm viabilityof semen ram cryopreserved. Was used seven ejaculates of six ram,which were pooled in pool, according to theexperimental groups: T1 - control; T2 - 1x10-7 mol / L and T3 - 1x10-9 mol / L melatonin. Posteriorly thediluting the samples were packaged in straws of 0.25 ml and cryopreserved. After thawing at 37°C for 30seconds, the samples were analyzed for Test thermoresistance slow (TTR) and acrosomal membrane integrity.For statistical analysis we used the Duncan test (α = 0.05) for mean comparison. The results demonstrated thatto the TTR at time 0 min, T2 showed 54.28% motility, and T1obtained lower values in the times 0 and 60 minutesfor force. Supplementation of 1x10-9mol / L of melatonin improved total motility.(AU)

Angiotensina-(1-7): Efeito na maturação in vitro de oócitos ovinos / Angiotensin- (1-7): Effect on in vitro maturation of sheep oocytes

Aimed to evaluate the effect of addition of angiotensin-(1-7) in the middle of in vitro maturation ofsheep oocytes. Seventy-four oocytes of sheep ovaries slaughtered in fridg were matured in vitro: I - control(n=22), II - Ang-(1-7) at 1 uM (n=24), III - Ang-(1-7) at 1 uM+A-779 at 1uM (n=28) in microdropletscontaining 100 µL of maturation medium plus 10% fetal bovine serum under mineral oil in the incubatoratmosphere 5% CO2 in air at 38.5°C for a period of 18 hours. After this period, the oocytes were denuded andobserved the extrusion of the first polar body. Statistical analysis was performed using the t test at 5%probability. The addition of angiotensin-(1-7) at 1 uM, as well as the addition of angiotensin-(1-7) at 1 uMtogether with its specific antagonist A-779 at the same concentration, decrease the in vitro maturation rate ovine oocytes.(AU)

Maturação de oócitos bovinos em meio suplementado com captopril / Maturation of Bovine oocytes in medium supplemented with captopril

The aim of this research was to evaluate the effects of supplementation of maturation medium withcaptopril in oocyte in vitro maturation (IVM). 470 CCOs were recovered and classified into grades I and II,being divided into four groups: G1 (n = 56), that was control group; G2 (n = 152) 20 mM of captopril; G3 (n =126) 40 uM of captopril; and G4 (n = 136) 80 uM of captopril, then these were subsequently submitted to IVMprocess for 24 hours at 38.5°C in 5% CO2. After 24 hours of maturation, oocytes were denuded and evaluatedfor the first polar body extrusion and were, therefore, considered matured. The addition of the Captopril inmedium of oocytes maturation has not improved the IVM rate.(AU)

Efeito do Inibidor do ativador do plasminogênio 1 (PAI-1) nos parâmetros cinéticos de espermatozoides criopreservados de touros Curraleiro Pé Duro / Inhibitor effect of plasminogen activator 1 (PAI-1) in the kinetic parameters of sperm cryopreserved of Curraleiro Pé-Duro bulls

This study was conducted to evaluate the effect of different plasminogen activator inhibitor 1concentrations (70 ƞg, 140 and 210 ƞg ƞg) in the kinetic parameters of sperm cryopreserved of Curraleiro FootHard bulls. Sperm kinetics were analyzed by means of a computer aided system (CASA). The variables evaluatedwere: (MT-%) (MOP-um / s), (VCL - um / s), (VSL - um / s), (VAP-um / s), (LIN -%) ( Str-%) (ALH - uM)Wobble (WOB -%) and (BCF-Hz). The cryopreserved sperm in the presence of the inhibitor of plasminogenactivator 1 in a concentration of 210 ƞg decreased velocity parameters in a straight line (VSL - um / s) andlinearity (LIN -%). In conclusion, supplementation of the Inhibitor of plasminogen activator 1 (PAI-1),cryopreservation of bovine semen does not improve the kinetic parameters as compared to the control.(AU)

Captopril na produção in vitro de embriões bovinos? / Captopril in production in vitro of embryos bovine?

Objective to evaluate the effect of captopril in vitro production of bovine embryos. 472 COCs were usedfrom abattoir ovaries, which were screened, sorted and selected in grades I and II, and submitted to the PIVprocess. The IVM treatments were added in the following concentrations: T1 - control; T2 - 5 mM of captopril;T3 - 10 uM of captopril; and T4 - 15 captopril uM, the COCs were subjected to IVM, IVF CIV. The results showthat there was no statistically significant difference (P > 0.05) between treatments during maturation. Thevariables studied were cleavage and blastocyst rates. The captopril supplementation did not improve (P > 0.05)G1 cleavage rate - 61.84%; G2 - 71.00%; G3 - 68.87%; and G4 - 56.90%. Supplementation of 20μM ofcaptopril influenced the amount of viable embryos.(AU)

Efeito do captopril na maturação in vitro de oócitos bovinos / Effect of captopril in maturation in vitro of oocyte bovine

This study aimed to evaluate the effect of captopril on the in vitro maturation of oocytes. 1627 COCscattle slaughter houses were used, were subsequently screened, classified into grades I and II, according to themorphological quality, and submitted to the IVM process, distributed in four treatments: T1 - control; T2 - 5μMof captopril; T3 - 10μM of captopril; and T4 - 15μM of captopril, incubated in an incubator at 38.5 ° C with anatmosphere of 5% CO2. After 22 hours, the COCs were stripped to evaluate the rate of maturation, which wereas follows: T1 - 56.60% (120/212); T2 - 60.60% (240/396); T3 - 52.88% (174/329) and T4 - 58.30% (207/355).The results show that there was no statistically significant difference ( P> 0.05) between treatments duringmaturation, concluding that captopril supplementation did not affect the maturation of COCs.(AU)

Avaliação da integridade da membrana plasmática e do potencial de atividade mitocondrial de sêmen criopreservado de touros frente a ação do (Limoneno (R)-(+) / Evaluation of plasma membrane integrity and mitochondrial activity potential of cryopreserved semen of bulls on action of the Limonene (R) - (+)

This study was conducted to evaluate the effect of different concentrations of limonene (R)-(+) (50 µM,100 µM and 150 µM) in supplementing the diluter of bulls freezing semen. Thirty-six ejaculated from fourCurraleiro-Pé-Duro bulls were used for cryopreservation. The epifluorescence microscopy was used todetermine the plasmatic integrity and mitochondrial activity potential. No was observed effect on the integrity ofplasma membrane nor mitochondrial activity potential when cryopreserved by adding limonene R - (+). Theresults obtained in this study allow to conclude that supplementation limonene (R) - (+) on diluter of bullsfreezing semen does not interfere with the integrity of the plasma membrane or the potential of spermmitochondrial activity.(AU)

Ação do Limoneno (S)-(-) sobre a cinética espermática de sêmen criopreservado de touros / Action of the Limonene (S) - (-) on sperm kinetics of cryopreserved semen of bulls

This study was conducted to evaluate the effect of different concentrations of Limoneno (S)-(-) (50 µM,100 µM and 150 µM) in supplementing the diluter of bulls freezing semen. Thirty-six ejaculated from fourCurraleiro-Pé-Duro bulls were used for cryopreservation. The cryopreserved spermatozoa were submitted to postthawmotility sperm of computer assisted analysis (CASA) to evaluate the characteristics of spermatic kinetics.Observed that The different concentrations of limonene (S) - (-) did not affect the parameters of kinetics spermaticexcept for linearity (LIN). The addition of 150 μM limonene (S) - (-) significantly increased (P <0.05) the LINcompared to the control. The results obtained in the present study allow us to conclude that the supplementationof limonene (S) - (-) in cryopreservation bovine semen diluent did not interfere in kinetics sperm.(AU)

Produção in vitro de embriões bovinos em meio suplementado com captopril / In vitro production of embryos Cattle in medium supplemented with captopril

The aim of this study was to evaluate the effects of supplementation of maturation medium withcaptopril, and its consequences in the bovine maturation, fertilization and embryo development in vitro. 326bovine ovaries from a local slaughterhouse were used. 1101 CCOs were recovered and distributed in fourgroups: G1 (n = 112), that was control group; G2 (n = 322) 20μM of captopril; G3 (n = 367) 40μM ofcaptopril; and G4 (n = 300) captopril 80μM and later submitted to IVM. The matured CCOs were fertilized, andco-incubated. After fertilization, 676 presumptive zygotes were cultured and maintained in the greenhouse for 7days. The total number of viable embryos was 12; 39; 32 and 31, respectively in the experimental groups.Considering the experimental conditions adopted, it was concluded that the addition of the Captopril in mediumof oocytes IVM positively doesnt influence embryonic development, as evidenced by the similar percentages ofembryo production.(AU)

Uso do diluidor ACP102® com e sem gema de ovo no sêmen resfriado de ovinos / Use of ACP102® extender with and without egg yolk in sheep cooled semen

This study aims to evaluate the fertility rate of sheep semen diluted and cooled to 4ºC in powdercoconut water (ACP-102®) with and without egg yolk in artificial insemination by cervical route in sheep. Tworam lambs and 72 ewe lambs were used, divided into 3 groups: ACP-102® without egg yolk and cooled to 4ºCfor 12 hours, ACP-102® with 2,5% egg yolk also cooled as the first group and a control group with fresh semendiluted in ACP-102® without egg yolk. Pregnancy diagnosis was performed 30 days later. Pregnancy rates weresignificantly different (P < 0.05) between ACP-SGF (58,3%) and ACP-SG4 (20,8%) groups. The ACP-CG4(37,5%) group did not differ in relation to the ACP-SGF. Therefore, the addition of egg yolk to ACP-102®extender favors the viability of sheep semen, cooled to 4ºC for 12 hours and fertility of artificially inseminatedsheep by cervical route.(AU)

Ação do Limoneno (S)-(-) sobre a cinética espermática de sêmen criopreservado de touros / Action of the Limonene (S) - (-) on sperm kinetics of cryopreserved semen of bulls

This study was conducted to evaluate the effect of different concentrations of Limoneno (S)-(-) (50 µM,100 µM and 150 µM) in supplementing the diluter of bulls freezing semen. Thirty-six ejaculated from fourCurraleiro-Pé-Duro bulls were used for cryopreservation. The cryopreserved spermatozoa were submitted to postthawmotility sperm of computer assisted analysis (CASA) to evaluate the characteristics of spermatic kinetics.Observed that The different concentrations of limonene (S) - (-) did not affect the parameters of kinetics spermaticexcept for linearity (LIN). The addition of 150 μM limonene (S) - (-) significantly increased (P <0.05) the LINcompared to the control. The results obtained in the present study allow us to conclude that the supplementationof limonene (S) - (-) in cryopreservation bovine semen diluent did not interfere in kinetics sperm.

Avaliação da integridade da membrana plasmática e do potencial de atividade mitocondrial de sêmen criopreservado de touros frente a ação do (Limoneno (R)-(+) / Evaluation of plasma membrane integrity and mitochondrial activity potential of cryopreserved semen of bulls on action of the Limonene (R) - (+)

This study was conducted to evaluate the effect of different concentrations of limonene (R)-(+) (50 µM,100 µM and 150 µM) in supplementing the diluter of bulls freezing semen. Thirty-six ejaculated from fourCurraleiro-Pé-Duro bulls were used for cryopreservation. The epifluorescence microscopy was used todetermine the plasmatic integrity and mitochondrial activity potential. No was observed effect on the integrity ofplasma membrane nor mitochondrial activity potential when cryopreserved by adding limonene R - (+). Theresults obtained in this study allow to conclude that supplementation limonene (R) - (+) on diluter of bullsfreezing semen does not interfere with the integrity of the plasma membrane or the potential of spermmitochondrial activity.

Captopril na produção in vitro de embriões bovinos? / Captopril in production in vitro of embryos bovine?

Objective to evaluate the effect of captopril in vitro production of bovine embryos. 472 COCs were usedfrom abattoir ovaries, which were screened, sorted and selected in grades I and II, and submitted to the PIVprocess. The IVM treatments were added in the following concentrations: T1 - control; T2 - 5 mM of captopril;T3 - 10 uM of captopril; and T4 - 15 captopril uM, the COCs were subjected to IVM, IVF CIV. The results showthat there was no statistically significant difference (P > 0.05) between treatments during maturation. Thevariables studied were cleavage and blastocyst rates. The captopril supplementation did not improve (P > 0.05)G1 cleavage rate - 61.84%; G2 - 71.00%; G3 - 68.87%; and G4 - 56.90%. Supplementation of 20μM ofcaptopril influenced the amount of viable embryos.

Efeito do captopril na maturação in vitro de oócitos bovinos / Effect of captopril in maturation in vitro of oocyte bovine

This study aimed to evaluate the effect of captopril on the in vitro maturation of oocytes. 1627 COCscattle slaughter houses were used, were subsequently screened, classified into grades I and II, according to themorphological quality, and submitted to the IVM process, distributed in four treatments: T1 - control; T2 - 5μMof captopril; T3 - 10μM of captopril; and T4 - 15μM of captopril, incubated in an incubator at 38.5 ° C with anatmosphere of 5% CO2. After 22 hours, the COCs were stripped to evaluate the rate of maturation, which wereas follows: T1 - 56.60% (120/212); T2 - 60.60% (240/396); T3 - 52.88% (174/329) and T4 - 58.30% (207/355).The results show that there was no statistically significant difference ( P> 0.05) between treatments duringmaturation, concluding that captopril supplementation did not affect the maturation of COCs.