J. Shetty et al., PITUITARY GONADOTROPINS REGULATE SPERMATOGONIAL DIFFERENTIATION AND PROLIFERATION IN THE RAT, Journal of Biosciences, 21(1), 1996, pp. 81-92
The relative regulatory roles of the pituitary gonadotropins, luteiniz
ing hormone and follicle stimulating hormone in the spermatogonial pro
liferation has been studied using specific antibodies against these ho
rmones in the immature rats. Immunoneutralization of luteinizing hormo
ne for 7 days resulted in significant reduction in tetraploid cells an
d total absence of haploid cells, while there was a relative increase
in the diploid population. This was also accomopanied by a decrease in
spermatogonial proliferation as indicated by a decrease in [H-3] thym
idine incorporation into DNA by purified spermatogonia. Administration
bf follicle stimulating hormone als for 7 days also caused a signific
ant decrease in the rate of spermatogonial proliferation. Withdrawal o
f follicle stimulating hormone led to a significant reduction in tetra
ploid and haploid cells However interestingly, it failed to totally ab
olish the appearance of these cells. Administration of testosterone (3
mg/day/rat) for 2 days along with the gonadotropin a/s could partially
reverse the effect on spermatogonial proliferation. It is concluded t
hat (i) both luteinizing hormone and follicle stimulating hormone are
involved in spermatogonial proliferation, (ii) lack of testosterone co
nsequent of the neutralization of luteinizing hormone prevented the en
try of spermatogonial cells into meiosis, (iii) testosterone may be in
volved in spermatogonial proliferation providing a mitotic signal and
(v) both follicle stimulating hormone and testosterone act synergistic
ally and lack of any one of the hormones results in impairment of sper
matogonial proliferation.