Effects of in vitro storage time and semen-extender on membrane quality of boar sperm assessed by flow cytometry

被引:54
作者
Waterhouse, KE
De Angelis, PM
Haugan, T
Paulenz, H
Hofmo, PO
Farstad, W
机构
[1] Team Semin, N-0033 Oslo, Norway
[2] Norwegian Sch Vet Sci, Dept Prod Anim Clin Sci, N-0033 Oslo, Norway
[3] Norsvin AI Ctr, N-2304 Hamar, Norway
[4] Natl Hosp Norway, Inst Pathol, N-0027 Oslo, Norway
关键词
boar; sperm quality; liquid semen storage; flow cytometry;
D O I
10.1016/j.theriogenology.2004.03.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Norwegian AI company Norsvin has used the short-term semen-extender BTS to extend and store boar semen since the late 1980s. Fertility results have been consistent when extended semen has been used for AI within 3 days after collection, however, from a production and economic point of view it is preferable that semen stored for up to 5 days can be used. The aim of this study was to compare membrane quality of sperm stored in BTS for 3 days with sperm stored in the long-term semen-extenders Androstar, Mulberry III and X-Cell (TM) for 5 days. Using a split-sample design, plasma membrane- and acrosome-integrity were assessed flow cytometrically by use of Yo-Pro-1 and PNA-FITC, and fluidity and phospholipid asymmetry of the membrane were assessed by use of MC540 and Annexin V-FITC. Due to observed sperm fragmentation in Androstar after Day 1, the data for Androstar were excluded from the analyses. After 5 days of storage, the membrane quality of X-cell (TM)-stored sperm was not statistically different from that of sperm stored in BTS for 3 days, while membrane quality of sperm stored in Mulberry III was statistically better on Day 5 compared to BTS on Day 3. In conclusion, Mulberry III and X-Cell (TM) preserve sperm quality, as well as that of BTS on Day 3, for up to 5 days after collection. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1638 / 1651
页数:14
相关论文
共 30 条
  • [1] The effect of storage time and number of spermatozoa per insemination dose on semen characteristics and fertilizing capacity of boar semen diluted with Beltsville Thaw Solution (BTS) extender
    Alexopoulos, C
    Boscos, C
    Saratsis, P
    Saoulidis, C
    Kyriakis, S
    [J]. ANIMAL SCIENCE, 1996, 62 : 599 - 604
  • [2] Sperm apoptosis in fresh and cryopreserved bull semen detected by flow cytometry and its relationship with fertility
    Anzar, M
    He, LW
    Buhr, MM
    Kroetsch, TG
    Pauls, KP
    [J]. BIOLOGY OF REPRODUCTION, 2002, 66 (02) : 354 - 360
  • [3] Oxidation of unsaturated phospholipids in membrane bilayer mixtures is accompanied by membrane fluidity changes
    Borst, JW
    Visser, NV
    Kouptsova, O
    Visser, AJWG
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2000, 1487 (01): : 61 - 73
  • [4] DACHARYPRIGENT J, 1993, BLOOD, V81, P2554
  • [5] EDDY EM, 1994, PHYSL REPRODUCTION, V1, P29
  • [6] Dynamics of the mammalian sperm plasma membrane in the process of fertilization
    Flesch, FM
    Gadella, BM
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON BIOMEMBRANES, 2000, 1469 (03): : 197 - 235
  • [7] Use of lectins to characterize plasma membrane preparations from boar spermatozoa: A novel technique for monitoring membrane purity and quantity
    Flesch, FM
    Voorhout, WF
    Colenbrander, B
    van Golde, LMG
    Gadella, BM
    [J]. BIOLOGY OF REPRODUCTION, 1998, 59 (06) : 1530 - 1539
  • [8] Flesch FM, 2001, J CELL SCI, V114, P3543
  • [9] Gadella BM, 2000, DEVELOPMENT, V127, P2407
  • [10] Capacitation induces cyclic adenosine 3′,5′-monophosphate-dependent, but apoptosis-unrelated, exposure of aminophospholipids at the apical head plasma membrane of boar sperm cells
    Gadella, BM
    Harrison, RAP
    [J]. BIOLOGY OF REPRODUCTION, 2002, 67 (01) : 340 - 350