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Acta Scientiae Veterinariae, <strong>2011</strong>. 39(Suppl 1): Abstracts - <strong>25th</strong> <strong>Annual</strong> <strong>Meeting</strong> <strong>SBTE</strong>-Brazil. August <strong>2011</strong>.<br />

A029 MALE REPRODUCTIVE PHYSIOLOGY AND SEMEN TECHNOLOGY<br />

EFFECTS OF SELENIUM AND CHROMIUM ON SEMINAL QUALIT<br />

ALITY OF BUFF<br />

UFFAL<br />

ALOES SUPPLEMENTED WITH BYPRODUCT<br />

ODUCTS OF<br />

AMAZONIAN AGROINDUSTRY<br />

Alessandra Ximenes Santos 1 , Alexandre Rossetto Garcia 2 , Cristian Faturi 3 , Benjamim De Souza Nahúm 4 , José Brito Lourenço Junior 5 , Sâmia Rubielle Silva De<br />

Castro 6 , Geanne Rocha Silva 7 & Arnaldo Algaranhar Gonçalves 8<br />

1,7,8<br />

UNIVERSIDADE FEDERAL DO PARÁ, BELEM, PA, BRAZIL. 2,4 EMBRAPA AMAZÔNIA ORIENTAL, BELÉM, PA, BRAZIL. 3 UNIVERSIDADE FEDERAL RURAL DA AMAZÔNIA, BELÉM, PA,<br />

BRAZIL. 5 UNIVERSIDADE DO ESTADO DO PARÁ, BELÉM, PA, BRAZIL. 6 FACULDADES INTEGRADAS DO TAPAJÓS, SANTARÉM, PB, BRAZIL.<br />

The use of organic industrial byproducts available on Amazon, such as coconut meal (CM) and palm kernel cake (PKC), may<br />

constitute an bioeconomic alternative to replace conventional concentrates for ruminants, leading to environmental and productive gains.<br />

Therefore, the aim was to evaluate the semen quality of buffalo supplemented daily with experimental diets based on PKC or CM, with different<br />

levels of selenium (Se) and chromium (Cr) intake. Fifteen buffaloes (3.2±1.8 years, 578.6±101.9 kg) raised on pasture (Panicum maximum) at<br />

the Embrapa Eastern Amazon were daily supplemented with isoproteic concentrates (1% BW) during 252 days. Animals had similar initial<br />

semen quality and were divided into three groups: Control (5 bulls; conventional ration with 62% corn grain), T1 (5 bulls; ration with 69.3%<br />

CM) and T2 (5 bulls; ration with 69.3% of PKC). Bulls had semen collected weekly, starting 112 days after first day of supplementation and two<br />

complete spermatogenic cycles, according to Sharma and Gupta (1980, Animal Reproduction Science, 3, 217-224). The ejaculates (n = 173)<br />

were evaluated for sperm motility, integrity of plasma membrane and sperm morphology. The level of Se and Cr in the feedstuffs was determined<br />

according to EPA-Method 7742/6010 (2009, U.S. Environmental Protection Agency, 26p). Data were subjected to ANOVA, with comparison<br />

by t test and the association between variables was analyzed by Pearson correlation (P < 0.05). The average of daily intake of Se (mg/day) for<br />

Control, T1 and T2 was 1.37±0.35 B , 1.15±0.26 C and 2.80±0.66 A (P < 0.05), respectively. Daily consumption of Cr (mg/day) in Control, T1 and<br />

T2 was 7.17±1.87 B , 4.30±0.97 C and 20.75±4.94 A (P < 0.05), respectively. Sperm motility was significantly higher (P < 0.05) in T2 (71.7±15.1% A )<br />

compared to Control (59.3±20.5% B ) and T1 (56.7±24 8% B ). Higher level of plasma membrane integrity (P < 0.05) was also observed in T2<br />

(82.1±12.2% A ) compared to T1 (72.0±22.6% B ) and Control (69.2±19.4% B ). There was no significant difference in the sperm total defects<br />

(Control: 44.2±18.5%, T1: 41.3±16.1% and T2: 44.3±19.2%). Correlation between consumption of Se and Cr with sperm motility (r=0.36 and<br />

r=0.34, P < 0.0001) and with plasma membrane integrity (r=0.33 and r=0.32, P < 0.0001) were significant and of medium intensity. Thus it can<br />

be concluded that selenium and chromium presented positive effects on preservation of plasma membrane integrity and on sperm motility, but<br />

had no interference on cellular morphology.<br />

[Acknowledgments. Project “Network for Innovation in Animal Reproduction” (01.07.01.002)].<br />

Keywords: semen, micronutrients, bubalus bubalis.<br />

A030 MALE REPRODUCTIVE PHYSIOLOGY AND SEMEN TECHNOLOGY<br />

EFFICIENCY OF THE CAP<br />

APACIT<br />

CITATING TING MEDIA ON MOTILIT<br />

TILITY MAINTENANCE AND INDUCTION OF EQUINE<br />

SPERMATOZ<br />

OZOA HYPERACTIV<br />

CTIVATION<br />

TION<br />

Daniela Franco da Silva, Rubens Paes de Arruda, Thayna Pantoja Gardes, Rafaela Nogueira Rodrigues Cardoso, Juliana<br />

Nascimento, Henrique Fulaneti Carvalho, Kleber Menegon Lemes & André Furugen Cesar de Andrade<br />

N<br />

USP, PIRASSUNUNGA, SP, BRAZIL.<br />

Hyperactivation is characterized by a non-progressive sperm trajectory and an overt lateral displacement of the head, which is<br />

essential for the occurrence of penetration of the zona pellucida (Suarez, 2008; Human Reproduction Update, 14 (6), 647-57). The aim of this<br />

study was to test by CASA, the capacitating media F (Andrade et al., 2008; Animal Reproduction Science, 107, 304-5) and the capacitating media<br />

M (MCPARTLIN et al., 2008; Theriogenology, 69, 639-50) in equine spermatozoa, in order to determine which was most efficient in promoting<br />

hyperactivation after 5 h of incubation. Three ejaculates from three stallions was collected and cryopreserved (n = 9). The semen was thawed,<br />

selected in Percoll ® and tested in the two media. The motion characteristics analyzed by CASA were total motility (MT%) and progressive<br />

motility (MP%) after 0, 30, 60, 120 and 300 min of incubation at 38°C and 5% CO2. In addition, there were adjustments of the tool Edit / Sort<br />

to assess the percentage of hyperactivated cells. The equine sperm was considered as hyperactivated when VCL> 180 µm and ALH > 12 µm<br />

(Rathi et al., 2001; Biology of Reproduction 65, 462-470). The data were analyzed using ANOVA and Tukey test and are presented as mean and<br />

standard deviation. The mean value of MT in medium F was 64.23±19.22%; 58.9±21.74%; 49.38±13.21%; 47.23±15.44% and 28.44±10.22%<br />

in time 0, 30, 60, 120 300 respectively. The medium M mean value was 62.43±21.19%; 52.94±22.90%; 49.8±18.8%; 43.46±17.94% e<br />

22.51±11.41%. The MP values of medium F in time 0, 30, 60, 120 e 300 min were 50.17±15.81%; 45.27±17.78%; 39.20±9.93%; 37.91±13.41%;<br />

24.37±9.92%, respectively. The MP mean values of the M medium was 48.87±18.30; 43.18±19.35%; 41.52±16.26%; 36.20±15.62%;<br />

19.61±9.11%. There was no interaction between treatment and incubation time regarding to sperm hyperactivity variable and the results was<br />

higher in medium F 8.48±4.38%; 7.66±4.92%; 7.68±6.73; 6.86±4.65% e 4.84±4.52% when it was compared with the mean values of medium<br />

M 6.85±1.41%; 6.00±2.83%; 5.11±2.21%; 4.39±3.19% e 2.35±2.40%. There were no differences between the two tested medium. Although<br />

both medium was considered efficient in maintaining sperm motion characteristics after 300 min of incubation, the F medium was better in<br />

inducing hyperactivation of sperm cells. [We thank Fundação de Amparo à pesquisa do Estado de São Paulo – FAPESP (Process: 09/54906-<br />

5, 09/50474-3, 10/01912-5, 10/01916-0). We thank Botu-Pharma that kindly donated the cryoprotectant for this experiment].<br />

Keywords: capacity, hyperactivation, spermatozoa.<br />

s351

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