Control of human luteal steroidogenesis: role of growth hormone-releasing hormone, vasoactive intestinal peptide, and pituitary adenylate cyclase-activating peptide
- PMID: 9418704
- DOI: 10.1016/s0015-0282(97)00370-1
Control of human luteal steroidogenesis: role of growth hormone-releasing hormone, vasoactive intestinal peptide, and pituitary adenylate cyclase-activating peptide
Abstract
Objective: To examine the possible effect of growth hormone-releasing hormone (GHRH), vasoactive intestinal peptide, and pituitary adenylate cyclase-activating peptide on basal and hCG-stimulated P production by human luteal cells.
Design: Cultures of human luteal cells from the early and midluteal phase.
Setting: All corpora lutea were obtained from the Obstetrics and Gynecology Department of the Università Cattolica, a public care center.
Patient(s): Ten nonpregnant women between 35 and 47 years of age underwent surgery for various nonendocrine disorders, such as leiomyomatosis.
Intervention(s): Corpora lutea were obtained at the time of hysterectomy.
Main outcome measure(s): Luteal cells were incubated with GHRH, vasoactive intestinal peptide, and pituitary adenylate cyclase-activating peptide with or without hCG at different concentrations.
Result(s): Pituitary adenylate cyclase-activating peptide stimulated P production in a dose- and time-dependent manner, whereas GHRH and vasoactive intestinal peptide did not affect luteal steroidogenesis. None of the three peptides were found to synergize with hCG.
Conclusion(s): Pituitary adenylate cyclase-activating peptide can influence human luteal steroidogenesis.
Similar articles
-
Neuropeptides of the pituitary adenylate cyclase-activating polypeptide/vasoactive intestinal polypeptide/growth hormone-releasing hormone/secretin family in testis.Endocrine. 2003 Apr;20(3):201-14. doi: 10.1385/ENDO:20:3:201. Endocrine. 2003. PMID: 12721498 Review.
-
Human growth hormone enhances progesterone production by human luteal cells in vitro. II. Evidence of a distinct effect on two luteal cell types.Fertil Steril. 1993 Jul;60(1):47-52. doi: 10.1016/s0015-0282(16)56034-8. Fertil Steril. 1993. PMID: 8513958
-
Human growth hormone enhances progesterone production by human luteal cells in vitro: evidence of a synergistic effect with human chorionic gonadotropin.Fertil Steril. 1992 Jan;57(1):92-6. doi: 10.1016/s0015-0282(16)54782-7. Fertil Steril. 1992. PMID: 1730337
-
Pituitary adenylate cyclase-activating polypeptide stimulates steroidogenesis and adenosine 3',5'-monophosphate accumulation in cultured rat granulosa cells.Endocrinology. 1994 Jul;135(1):207-13. doi: 10.1210/endo.135.1.8013355. Endocrinology. 1994. PMID: 8013355
-
Structural simplification of potent growth hormone-releasing hormone analogs: implications for other members of the VIP/GHRH/PACAP family.Ann N Y Acad Sci. 1996 Dec 26;805:149-58. doi: 10.1111/j.1749-6632.1996.tb17480.x. Ann N Y Acad Sci. 1996. PMID: 8993400 Review. No abstract available.
Cited by
-
Female reproductive functions of the neuropeptide PACAP.Front Endocrinol (Lausanne). 2022 Sep 20;13:982551. doi: 10.3389/fendo.2022.982551. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36204113 Free PMC article. Review.
-
Role of PACAP in Female Fertility and Reproduction at Gonadal Level - Recent Advances.Front Endocrinol (Lausanne). 2012 Dec 11;3:155. doi: 10.3389/fendo.2012.00155. eCollection 2012. Front Endocrinol (Lausanne). 2012. PMID: 23248616 Free PMC article.
-
Neuropeptides of the pituitary adenylate cyclase-activating polypeptide/vasoactive intestinal polypeptide/growth hormone-releasing hormone/secretin family in testis.Endocrine. 2003 Apr;20(3):201-14. doi: 10.1385/ENDO:20:3:201. Endocrine. 2003. PMID: 12721498 Review.
-
Correlation between oocyte number and follicular fluid concentration of pituitary adenylate cyclase-activating polypeptide (PACAP) in women after superovulation treatment.J Mol Neurosci. 2012 Nov;48(3):617-22. doi: 10.1007/s12031-012-9743-3. Epub 2012 Mar 14. J Mol Neurosci. 2012. PMID: 22415357
MeSH terms
Substances
LinkOut - more resources
Full Text Sources