Cryopreservation of canine epididymal sperm using ACP-106c and TRIS

被引:23
作者
Mota Filho, Antonio Cavalcante [1 ]
Rodrigues Silva, Herlon Victor [1 ]
Pereira Nunes, Thalles Gothardo [2 ]
de Souza, Mirley Barbosa [1 ]
de Freitas, Luana Azevedo [1 ]
de Araujo, Airton Alencar [3 ]
Machado da Silva, Lucia Daniel [1 ]
机构
[1] Univ Estadual Ceara, Sch Vet Med, Lab Carnivore Reprod, BR-1700 Fortaleza, Ceara, Brazil
[2] Univ Estadual Ceara, Sch Vet Med, Lab Swine Semen Technol, BR-1700 Fortaleza, Ceara, Brazil
[3] Univ Fed Ceara, Fac Zootecnia, BR-60021970 Fortaleza, Ceara, Brazil
关键词
Cryopreservation; Epididymis; Dog; Sperm; VITRO MATURED OOCYTES; BOVINE SPERMATOZOA; FROZEN; RECOVERY; QUALITY; INSEMINATION; PARAMETERS; FERTILITY; INJECTION; EXTENDERS;
D O I
10.1016/j.cryobiol.2014.04.013
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The objective was to cryopreserve sperm recovered from the canine epididymal cauda immediately after an orchiectomy. The sperm was stored for 12 h at 4 degrees C using ACP-106c and TRIS as extenders. Sixty adult male dogs were used. The testis-epididymis complex (TEC) was removed, immersed in 0.9% saline and transported to the laboratory. The 60 TEC were divided into groups according to the 4 degrees C cooling time (Oh or 12 h) and according to the extender used for sperm recovery (ACP-106c or TRIS), forming 4 experimental groups: G0h-ACP, G12h-ACP, G0h-TRIS and G12h-TRIS. The sperm were recovered from the epididymal cauda using the retrograde flow technique. Next, 1.0 mL of ACP-106c or 1.0 mL of TRIS (preheated to 37 degrees C for 5 min) was added to the sperm of each epididymis. One week later, the sperm was thawed at 37 degrees C for 1 min, and its morphology, functionality and total and progressive sperm motilities were analyzed. Other parameters were obtained by Computer Assisted Semen Analysis (CASA). The data were submitted to multivariate analysis of variance (MANOVA) (P < 0.05). The total motility values were 52.17 +/- 1.78 and 49.8 +/- 1.93 for groups G0h-ACP and G12h-ACP and 50.7 +/- 2.06 and 43.90 +/- 2.51 for groups G0h-TRIS and G12h-TRIS, respectively. A decrease in total sperm motility was observed after 12 h of cooling for both extenders (P < 0.05). ACP-106c can be used as an extender for freezing canine epididymal sperm, and the freezing procedure must be performed immediately after sperm recovery. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:17 / 21
页数:5
相关论文
共 35 条
  • [1] Arruda R.P., 2000, THESIS U SAO PAULO S
  • [2] Barbosa Claudia da Cunha, 2009, Ciencia Animal Brasileira, V10, P1207
  • [3] Intracytoplasmic sperm injection of in vitro matured oocytes of domestic cats with frozen-thawed epididymal spermatozoa
    Bogliolo, L
    Leoni, G
    Ledda, S
    Naitana, S
    Zedda, M
    Carluccio, A
    Pau, S
    [J]. THERIOGENOLOGY, 2001, 56 (05) : 955 - 967
  • [4] Cardoso J.F.S., 2010, COMUNICATA SCI, V1, P146
  • [5] Evaluation of fertilizing potential of frozen-thawed dog spermatozoa diluted in ACP-106® using an in vitro sperm-oocyte interaction assay
    Cardoso, R. C. S.
    Silva, A. R.
    Silva, L. D. M.
    Chirinea, V. H.
    Souza, F. F.
    Lopes, M. D.
    [J]. REPRODUCTION IN DOMESTIC ANIMALS, 2007, 42 (01) : 11 - 16
  • [6] CBRA, 1998, MAN EX ANDR AV SEM A, P49
  • [7] Cryopreservation of epididymal dog sperm
    Hewitt, DA
    Leahy, R
    Sheldon, IM
    England, GCW
    [J]. ANIMAL REPRODUCTION SCIENCE, 2001, 67 (1-2) : 101 - 111
  • [8] Holt C, 1997, J ANDROL, V18, P312
  • [9] Unilateral intrauterine insemination with prostatic fluid-sensitized frozen caudal epididymal sperm in beagle dogs
    Hori, T
    Hagiuda, K
    Kawakami, E
    Tsutsui, T
    [J]. THERIOGENOLOGY, 2005, 63 (06) : 1573 - 1583
  • [10] Cryopreservation and ensuing in vitro fertilization ability of boar spermatozoa from epididymides stored at 4°C
    Kikuchi, K
    Nagai, T
    Kashiwazaki, N
    Ikeda, H
    Noguchi, J
    Shimada, A
    Soloy, E
    Kaneko, H
    [J]. THERIOGENOLOGY, 1998, 50 (04) : 615 - 623