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Abstract
Teratozoospermia (ejaculation of < 40% morphologically
normal sperm) commonly occurs within the Felidae,
including certain domestic cats, but the cellular and
molecular mechanisms that give rise to this phenomenon
remain unknown. This study quantified spermatogenesis to
identify differential dysfunctions in teratospermic versus
normospermic (> 60% normal sperm/ejaculate) domestic cats.
Sperm used were from electroejaculates and cauda
epididymides. Testes from 10 normo- and 10 teratospermic
males were obtained by castration and then evaluated by
histomorphometry, flow cytometry, and testicular
testosterone EIA. Some morphometric traits (tubular
diameter, epithelium height, interstitial area, number of
Leydig cells and blood vessels per cross section) as well
as testicular testosterone concentrations were similar
between groups, but testicular volume was greater in
teratospermic males. Stage frequencies differed also
between both cat populations, suggesting possible
dysfunctions in spermiation. Quantification of cell
populations in most frequent stages revealed more
spermatogenic cells and fewer Sertoli cells per tubule
cross section as well as per tissue unit in teratospermic
donors. Hence, the ratio of spermatogenic cells per
Sertoli cell was elevated in the teratospermic cat. DNA
flow cytometry confirmed higher total spermatogenic and
meiotic transformations in teratospermic males. In
summary, compared to normospermic counterparts,
teratospermic cats have a higher sperm output achieved by
more sperm producing tissue, more germ cells per Sertoli
cell, and reduced germ cell loss during spermatogenesis.
Gains in sperm quantity are produced at the expense of
sperm quality.
Key words:
Testis
Sertoli cells
Sperm
Spermatid
Testosterone
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