Functional significance of the sperm head morphometric size and shape for determining freezability in Iberian red deer (Cervus elaphus hispanicus) epididymal sperm samples

被引:77
作者
Esteso, Milagros C.
Soler, Ana J.
Fernandez-Santos, Maria R.
Quintero-Moreno, Armando A.
Garde, Jose J.
机构
[1] UCLM, JCCM, CSIC, IREC,Natl Wildlife Res Inst, Albacete, Spain
[2] Univ Zulia, Fac Med Vet, Anim Prod Res Unit, Maracaibo 4011, Venezuela
[3] UCLM, Secc Recursos Cineget & Ganaderos, IDR, Dept Game Resources,Biol Reprod Grp, Albacete 02071, Spain
来源
JOURNAL OF ANDROLOGY | 2006年 / 27卷 / 05期
关键词
cryopreservation; morphology; postmortem recovery;
D O I
10.2164/jandrol.106.000489
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
In the present study, computer-automated sperm head morphometry of epididymal samples was used to determine if sperm head area and shape are useful measurements for separating "good" and "bad" Iberian red deer freezers. A microscope slide was prepared from single diluted sperm fresh samples collected from 38 mature stags. Slides were air-dried and stained with Hemacolor. The sperm head area and shape (length/width) for a minimum of 145 sperm heads were determined for each male by means of the Sperm-Class Analyser. The remainder of each sample was frozen. After thawing, sperm cryosurvival was judged in vitro by microscopic assessments of individual sperm motility and of plasma membrane and acrosome integrities. All sperm parameters evaluated at thawing were placed in a statistical database and a multivariate cluster analysis performed. Mean sperm parameters of the 2 clusters generated ("bad" and "good" freezers) were compared by ANOVA. Our results show that sperm quality at thawing for all sperm parameters evaluated was significantly higher (P < .01) for "good" freezers than for the "bad" ones (sperm motility index: 67.4 +/- 2.0 vs 57.1 +/- 2.8; NAR: 67.1 +/- 2.5 vs 54.5 +/- 3.5; viability: 68.8 +/- 42.0 vs 60.1 +/- 2.8; HOST: 71.3 +/- 2.2 vs 63.1 +/- 3.1). Additionally, differences (P < .01) in epidiclymal sperm head area and shape were found between "good" and "bad" freezers before freezing, with the smallest overall sperm head dimensions found in the "good" freezers group (area: 32.04 mu m(2) vs 34.42 mu m(2)). Thus, the lower the sperm head area in the fresh samples, the greater the sperm cryoresistance. Our results show that the 2 groups of males also differ in sperm head shape in fresh samples (good: 1.96 vs poor: 1.72; P < .01). It is possible that sperm head area and shape influence total sperm volume, thus causing differences in heat exchange as well as in movements of water, ions, and cryoprotectants and, in turn, on sperm freezability.
引用
收藏
页码:662 / 670
页数:9
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