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Calcitonin expression in rat anterior pituitary gland is regulated by ovarian steroid hormones.
- Source :
-
Endocrinology [Endocrinology] 2002 Oct; Vol. 143 (10), pp. 4056-64. - Publication Year :
- 2002
-
Abstract
- Gonadotroph-derived calcitonin-like peptide (pit-CT) is a potent inhibitor of lactotroph function. We investigated the effect of ovarian hormones on pit-CT mRNA expression in the anterior pituitary (AP) gland of cycling female rats. Levels of mRNAs for pit-CT, CT receptor, prolactin (PRL), and beta-LH during 4-d estrous cycle were determined. In a second study, the effects of estrogens and progesterone on pit-CT and PRL mRNA levels were investigated. In a third group, the effect of estrogen or progesterone depletion on pit-CT mRNA expression was studied. In a fourth group, the effect of passive pit-CT immunization on PRL and LH mRNA expression was examined. Pit-CT mRNA levels varied during estrous cycle. They were highest in diestrus, but lowest in the evening of proestrus. CT-receptor mRNA levels displayed smaller fluctuations. Estrogen repletion caused a decline in pit-CT mRNA expression in ovariectomized rats, but progesterone produced a marked increase. ICI 182,780 prevented the decline of pit-CT mRNA levels during late proestrus-estrus, but RU 486 attenuated pit-CT mRNA levels. Passive CT immunization in diestrus altered PRL and LH mRNA expression, and advanced the estrus cycle. These results suggest that pit-CT mRNA expression is regulated by ovarian hormones, and depletion of pit-CT advances their estrous cycle.
- Subjects :
- Animals
Calcitonin genetics
Calcitonin immunology
Estradiol analogs & derivatives
Estrogen Antagonists pharmacology
Estrus metabolism
Female
Fulvestrant
Hormone Antagonists pharmacology
Immunization, Passive
Mifepristone pharmacology
Ovariectomy
Progestins antagonists & inhibitors
Progestins immunology
Prolactin genetics
RNA, Messenger metabolism
Rats
Rats, Inbred F344
Receptors, Calcitonin genetics
Calcitonin metabolism
Estradiol pharmacology
Pituitary Gland, Anterior metabolism
Progesterone pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0013-7227
- Volume :
- 143
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 12239117
- Full Text :
- https://doi.org/10.1210/en.2001-210908