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Fundulus heteroclitus gonadotropin(s). I.
Homologous bioassay using oocyte maturation and steroid production by
isolated ovarian follicles.
Lin YW, Lamarca MJ,
Wallace RA.
Isolated ovarian follicles from several species
were cultured to develop an in vitro bioassay system for Fundulus
heteroclitus gonadotropin. An extract of F. heteroclitus pituitaries,
when tested in heterologous systems using follicles from Rana pipiens.
Xenopus laevis, and Carassius auratus, was ineffective in provoking
either germinal vesicle breakdown or steroid production. In a homologous
system using F. heteroclitus follicles, F. heteroclitus pituitary
extract was capable of inducing both germinal vesicle breakdown and
steroid production in a dose-dependent fashion. Testosterone,
estradiol-17 beta, and 17 alpha-hydroxy,20 beta-dihydroprogesterone were
detected in both the culture media and the follicle extracts after F.
heteroclitus pituitary extract stimulation. The steroidogenic responses
resulting from the pituitary extract stimulation were dependent on the
size and stage of follicular development. Only large vitellogenic
follicles (1.2-1.4 mm diameter) were able to produce 17 alpha-hydroxy,20
beta-dihydroprogesterone and testosterone. Small vitellogenic follicles
(less than 1.2 mm) were unresponsive to stimulation by F. heteroclitus
pituitary extracts as scored by either germinal vesicle breakdown or
production of 17 alpha-hydroxy, 20 beta-dihydroprogesterone and
testosterone. However, estradiol-17 beta production was detected in
follicles of a much wider size range: Follicles as small as 0.8 mm
diameter were responsive to F. heteroclitus pituitary extract
stimulation and produced a large quantity of estradiol-17 beta. There
was a marked seasonal sensitivity of F. heteroclitus follicles to
pituitary extract stimulation in vitro. Follicles obtained from fish
outside of the breeding season (January) were less responsive to
stimulation by pituitary extract or steroid. The same preparation of
pituitary extract was capable of provoking germinal vesicle breakdown in
follicles obtained in May. Pituitary extracts prepared during October
through January were also less potent than those prepared during the
breeding season (February through September). We conclude that F.
heteroclitus gonadotropin(s) shows a noticeable species specificity and
that F. heteroclitus follicles exhibit both a season- and a
size-dependent responsiveness to gonadotropin(s). Hence, with a
judicious use of the appropriate types of F. heteroclitus ovarian
follicles, we have been able to demonstrate that in vitro oocyte
maturation and steroid production are sensitive, homologous bioassays
for F. heteroclitus gonadotropin(s).
PMID: 3497837 [PubMed -
indexed for MEDLINE]
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