Abstract
A preclinical evaluation for reversal through a noninvasive approach following long-term
vas occlusion with styrene maleic anhydride (SMA) has been attempted in langur monkeys
at the level of semen parameters, sperm functional tests, semen biochemistry, histology
and ultrastructure of reproductive organs, hematology and serum clinical biochemistry
including antisperm antibodies (ASA), prostate-specific antigen (PSA) and testosterone.
Noninvasive reversal through palpation, percutaneous squeezing and electrical stimulation,
forced vibratory movements and suprapubic percussion in the inguinal segments and
per-rectal digital massage was attempted in seven langur monkeys after 540 days following
vas occlusion. The results revealed instant azoospermia reversal on the same day of
reversal with impaired sperm quality, which showed gradual improvement and normospermia
with normal motility and viability after 60���90 days of reversal. Sperm functional
tests, including ultrastructure of spermatozoa, indicative of sterility in the initial
ejaculations, reached normalcy after 90���120 days of reversal. The seminal plasma
biochemistry indicative of obstructive azoospermia regained a normal pattern after
90���120 days of reversal. The morphology of testes that showed focal degeneration
during 540 days of vas occlusion and that of vasa deferentia that showed exfoliation
of epithelial cells resumed to normal morphology comparable with control animals after
150 days of reversal. The morphology of the epididymis, seminal vesicle and prostate
did not show appreciable changes following vas occlusion and after noninvasive reversal
compared with those of control animals. Hematology, serum clinical chemistry, ASA,
PSA and testosterone fluctuated within control limits, indicating safety of the procedure
at the level of accessory reproductive organs. The results suggest that noninvasive
reversal is feasible even after long-term vas occlusion with SMA and is safe without
adverse side effects.
Keywords
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Article info
Publication history
Accepted:
August 24,
2004
Received in revised form:
August 18,
2004
Received:
June 24,
2004
Identification
Copyright
© 2005 Elsevier Inc. Published by Elsevier Inc. All rights reserved.