HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

On the primary site of action of estrogens and androgens in the regulation of hepatic prolactin receptors.

Abstract
The aim of the present study was to identify the primary sites of action of estrogens and androgens in the regulation of hepatic PRL receptors in the rat. Implantation of estradiol benzoate in the pituitary region of male rats caused a feminization (i.e. an increase) of PRL receptors to a concentration typical of that found in female rats. Estrogen implanted in the paraventricular region of male rats was less effective in causing such a feminization. Subcutaneous implantation of estrogen did not affect the PRL receptor concentration. It is concluded that estrogen induces PRL receptors via an action at the hypothalamo-pituitary level, possibly directly on the pituitary. The PRL receptor-suppressive action of sc injected testosterone was also exerted by the synthetic androgen R1881 (17 beta-hydroxy-17 alpha-methylestra-4,9,11-trien-3-one). However, anterior hypothalamic deafferentation rendered both male and female rats insensitive to this action of R1881. It is concluded that an intact hypothalamo-pituitary unit is required for the PRL receptor-suppressive action of R1991. It is possible that the site of action of androgens is in the rostral hypothalamus or in adjacent areas of the brain.
AuthorsG Norstedt, A Mode
JournalEndocrinology (Endocrinology) Vol. 111 Issue 2 Pg. 645-9 (Aug 1982) ISSN: 0013-7227 [Print] United States
PMID6284488 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Delayed-Action Preparations
  • Estrenes
  • Receptors, Cell Surface
  • Receptors, Prolactin
  • Metribolone
  • Testosterone
  • Estradiol
  • estradiol-17 beta-benzoate
Topics
  • Animals
  • Delayed-Action Preparations
  • Estradiol (administration & dosage, analogs & derivatives, pharmacology)
  • Estrenes (administration & dosage, pharmacology)
  • Female
  • Injections, Subcutaneous
  • Liver (metabolism)
  • Male
  • Metribolone
  • Rats
  • Receptors, Cell Surface (drug effects, metabolism)
  • Receptors, Prolactin
  • Testosterone (administration & dosage, pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: