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Effect of pituitary adenylate cyclase-activating polypeptide (PACAP) on progestin biosynthesis in cultured luteal cells from rat ovary

We examined the effects of pituitary adenylate cyclase-activating polypeptide (PACAP) on progestin biosynthesis in cultured luteal cells from rat ovary. Luteal cells from immature rats treated with pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG) were cultured in the ab...

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Published in:Gynecological endocrinology 2001, Vol.15 (3), p.184-191
Main Authors: Usuki, S., Kotani, E.
Format: Article
Language:English
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Summary:We examined the effects of pituitary adenylate cyclase-activating polypeptide (PACAP) on progestin biosynthesis in cultured luteal cells from rat ovary. Luteal cells from immature rats treated with pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG) were cultured in the absence or presence of ovine luteinizing hormone (LH) (100 ng/ml) and PACAP-38 (10 ,100 and 1000 ng/ml). Following 48 hours of incubation ,the levels of progesterone ,20α-hydroxy-4-pregnene-3-one (20α-OH-P) and adenosine 3′ ,5′-monophosphate (cAMP) were measured in the culture media. PACAP alone significantly stimulated the production of progesterone and 20α-OH-P in a dose-dependent manner (p < 0.01 and 0.05 ,respectively ,ANOVA). LH-induced production of progesterone and accumulation of cAMP were significantly decreased by increasing concentrations of PACAP (p < 0.05 for each ,ANOVA). Conversely ,LH-stimulated 20α-OH-P production was enhanced by PACAP in a dose-dependent manner (p < 0.05). Since PACAP decreased the ratio of progesterone to 20α-OH-P production in LH-stimulated cells ,PACAP-mediated inhibition of the stimulatory action of LH on progesterone production may be involved in the initiation of luteolysis. PACAP-38 also suppressed increases in LH receptor content in cultured luteal cells. These results suggest that PACAP regulates the effects of LH on luteal cell function and that PACAP might be closely linked to reproduction.
ISSN:0951-3590
1473-0766
DOI:10.1080/gye.15.3.184.191