Resumo
The objective of this study was to assess the effect of several solutions and incubation times in the hypoosmotic swelling test in predicting the in vitro quality of the frozen/thawed semen of Piau boars. Four samples of frozen semen from five different Piau boars were used. For the assessment of the hypoosmotic test, three incubation times were used (5, 30 and 60 min) in three different hypoosmotic solutions (BTS at 75 mOsm/Kg, sucrrose at 100 mOsm/Kg and fructose and sodium citrate at 100 mOsm/Kg), thus, samples were submitted to each hypoosmotic solution in three incubation times. The means of sperm motility spermatic vigor and live sperm by supravital staining for the assessed samples were respectively, 37.5 ± 7.2%, 2.8 ± 0.3 and 37.4 ± 7.8% in thawing and 15.5 ± 7.6%, 1.7 ± 0.5 and 22.6 ± 6.6% after 120 mm of thermoresistance test (P < 0.05). There was no difference between the mean values obtained for reactive sperm in the different incubation times and hypoosmotic solutions, and also no interaction between time ans solutions. The results obtained in the resent study demonstrated that quality of frozen/thawed semen, besides offering aliernatives for hypoosmotic solutions and different incubation times in performing the hypoosmotic test to predict the sperm plasmatic membrane quality in boats.
Assuntos
Animais , Incubadoras , Preservação do Sêmen/métodos , Análise do Sêmen/veterinária , Suínos/classificaçãoResumo
The objective of this study was to assess the effect of several solutions and incubation times in the hypoosmotic swelling test in predicting the in vitro quality of the frozen/thawed semen of Piau boars. Four samples of frozen semen from five different Piau boars were used. For the assessment of the hypoosmotic test, three incubation times were used (5, 30 and 60 min) in three different hypoosmotic solutions (BTS at 75 mOsm/Kg, sucrrose at 100 mOsm/Kg and fructose and sodium citrate at 100 mOsm/Kg), thus, samples were submitted to each hypoosmotic solution in three incubation times. The means of sperm motility spermatic vigor and live sperm by supravital staining for the assessed samples were respectively, 37.5 ± 7.2%, 2.8 ± 0.3 and 37.4 ± 7.8% in thawing and 15.5 ± 7.6%, 1.7 ± 0.5 and 22.6 ± 6.6% after 120 mm of thermoresistance test (P < 0.05). There was no difference between the mean values obtained for reactive sperm in the different incubation times and hypoosmotic solutions, and also no interaction between time ans solutions. The results obtained in the resent study demonstrated that quality of frozen/thawed semen, besides offering aliernatives for hypoosmotic solutions and different incubation times in performing the hypoosmotic test to predict the sperm plasmatic membrane quality in boats.(AU)