Literature DB >> 2992915

Adenylate cyclase in the corpus luteum of the rhesus monkey. III. Changes in basal and gonadotropin-sensitive activities during the luteal phase of the menstrual cycle.

K M Eyster, J S Ottobre, R L Stouffer.   

Abstract

The activity of adenylate cyclase was examined in corpora lutea (CL) obtained from rhesus monkeys at specific stages in the luteal phase of the menstrual cycle [3-5, 6-8, 9-12, 13-15, and 16 days (menses) after the midcycle LH surge]. The conversion of [alpha-32P]ATP to [32P]cAMP was used to monitor adenylate cyclase activity. cAMP production in luteal homogenates was assessed in the absence (basal activity) and presence of maximum stimulatory doses of forskolin (100 microM), 5'-guanylylimidodiphosphate [GMP-P(NH)P; 50 microM], GTP (50 microM), and GTP plus increasing doses of hLH and hCG. Basal activity was low in the early luteal phase (days 3-5; mean +/- SE, 1.2 +/- 0.2 pmol cAMP/mg protein X min), increased (P less than 0.05) by the midluteal phase (days 6-8 and 9-12, 2.1 +/- 0.4 and 2.0 +/- 0.3 pmol/mg X min, respectively), and then declined (P less than 0.05) during the late luteal phase (days 13-15 and 16-menses, 1.6 +/- 0.3 and 1.2 +/- 0.5 pmol/mg X min, respectively). Activity stimulated by GTP and GMP-P(NH)P [e.g. GMP-P(NH)P approximately 12 times basal level] followed the same pattern as basal activity during the luteal phase. In contrast, cAMP production in the presence of forskolin did not change significantly throughout the luteal phase. In the midluteal phase (days 6-8 and 9-12; n = 12), hCG and human LH (hLH) stimulated adenylate cyclase in a similar dose-dependent manner. Maximal stimulation of cAMP production by hCG was about 10% greater (P less than 0.05) than that by hLH; the activation constant was 12.3 nM for hCG and 28.3 nM for hLH. The maximal response to hLH and hCG as well as the sensitivity of adenylate cyclase to activation by hLH were greater (P less than 0.05) in the midluteal phase than in the early or late luteal phase. Decreased basal, gonadotropin-stimulated, and guanine nucleotide-stimulated cAMP production and diminished sensitivity of adenylate cyclase to hLH correlated with a decline (P less than 0.05) in circulating progesterone and luteal weight during the late luteal phase. Thus, the adenylate cyclase system of the rhesus monkey CL undergoes significant changes during the luteal phase which are associated with the development and regression of the CL of the menstrual cycle. Mechanisms that modulate gonadotropin and nucleotide activation of adenylate cyclase without interfering directly with the catalytic unit are implicated in the changes that accompany luteolysis.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2992915     DOI: 10.1210/endo-117-4-1571

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  9 in total

Review 1.  Analysis of microarray data from the macaque corpus luteum; the search for common themes in primate luteal regression.

Authors:  C V Bishop; R L Bogan; J D Hennebold; R L Stouffer
Journal:  Mol Hum Reprod       Date:  2010-09-20       Impact factor: 4.025

2.  Systematic determination of differential gene expression in the primate corpus luteum during the luteal phase of the menstrual cycle.

Authors:  Randy L Bogan; Melinda J Murphy; Richard L Stouffer; Jon D Hennebold
Journal:  Mol Endocrinol       Date:  2008-02-07

3.  Dynamic changes in gene expression that occur during the period of spontaneous functional regression in the rhesus macaque corpus luteum.

Authors:  Randy L Bogan; Melinda J Murphy; Jon D Hennebold
Journal:  Endocrinology       Date:  2008-10-23       Impact factor: 4.736

4.  Liver x receptor modulation of gene expression leading to proluteolytic effects in primate luteal cells.

Authors:  Randy L Bogan; Andrea E Debarber; Jon D Hennebold
Journal:  Biol Reprod       Date:  2012-03-30       Impact factor: 4.285

Review 5.  Endocrine and local control of the primate corpus luteum.

Authors:  Richard L Stouffer; Cecily V Bishop; Randy L Bogan; Fuhua Xu; Jon D Hennebold
Journal:  Reprod Biol       Date:  2013-09-14       Impact factor: 2.376

6.  In vivo responses of the primate corpus luteum to luteinizing hormone and chorionic gonadotropin.

Authors:  A J Zeleznik
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

7.  The reverse cholesterol transport system as a potential mediator of luteolysis in the primate corpus luteum.

Authors:  Randy L Bogan; Jon D Hennebold
Journal:  Reproduction       Date:  2010-01       Impact factor: 3.906

8.  Corpus luteum as a novel target of weight changes that contribute to impaired female reproductive physiology and function.

Authors:  Satu Kuokkanen; Alex J Polotsky; Justin Chosich; Andrew P Bradford; Anna Jasinska; Tzu Phang; Nanette Santoro; Susan E Appt
Journal:  Syst Biol Reprod Med       Date:  2016-05-17       Impact factor: 3.061

9.  The liver X receptors and sterol regulatory element binding proteins alter progesterone secretion and are regulated by human chorionic gonadotropin in human luteinized granulosa cells.

Authors:  Yafei Xu; José J Hernández-Ledezma; Scot M Hutchison; Randy L Bogan
Journal:  Mol Cell Endocrinol       Date:  2018-01-31       Impact factor: 4.102

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.