Author:
Maxwell W. M. C.,Evans G.,Mortimer S. T.,Gillan L.,Gellatly E. S.,McPhie C. A.
Abstract
The effect of seminal plasma (SP) on the motility, capacitation status,
penetration through cervical mucus and fertility of frozen–thawed ram
spermatozoa was examined. In the presence of SP, motility of
frozen–thawed spermatozoa was better (P<0.001)
and there were more uncapacitated and less acrosome-reacted cells in
comparison with controls (P<0.001).
Frozen–thawed spermatozoa were also better able to penetrate cervical
mucus after addition of SP. Addition of SP increased the percentage of ewes
pregnant after insemination of frozen–thawed (39/94, 41.5%
v. 51/92, 55.4%;
P<0.05) but not fresh spermatozoa (34/55,
61.8% v. 42/58, 72.4% for 0
v. 30% SP in the resuspension medium). Moreover,
SP improved pregnancy rates after cervical (14/50; 28%
v. 25/49; 51%;
P<0.05) but not intrauterine insemination (25/44;
56.8 v. 26/43; 60.5%) with
frozen–thawed spermatozoa. In a second experiment, pregnancy rates were
30/45 (66.7%), 9/37 (24.3%) and 24/40 (60.0%)
for ewes inseminated with frozen–thawed spermatozoa in the uterus
(control), cervix without SP and cervix after supplementation with SP,
respectively (P<0.01 for unsupplemented
v. supplemented spermatozoa). These experiments
demonstrate that impaired function of cryopreserved spermatozoa can be
overcome by addition of SP, resulting in normal fertility after cervical AI.
Subject
Developmental Biology,Endocrinology,Genetics,Molecular Biology,Animal Science and Zoology,Reproductive Medicine,Biotechnology
Cited by
118 articles.
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