Document Detail


Effect of chronic thyroxine treatment on pregnancy in rats: effects on oestrogen, progesterone, prolactin and GH receptors in uterus, liver and mammary gland.
MedLine Citation:
PMID:  9738703     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We have previously shown that experimental hyperthyroidism produces premature and difficult delivery and absence of lactation in spite of apparently adequate luteolysis and lactogenesis. To study the possible causes of these alterations we measured the effect of treatment with T4 (0.25 or 1 mg kg(-1), s.c., daily, started 10-15 days before mating, HT0.25 and HT1) on serum hormones and their receptor (R) concentrations in reproductive tissues on day 20 of pregnancy (1800 hours), comparing them with controls on the same day (C20), or on day 21 of pregnancy (1800 hours) (C21). Serum prolactin (PRL) and corticosterone (B) concentrations increased in the HT groups, progesterone (Pg) and GH decreased and estradiol (E2) did not change, compared with C20 group. C21 rats had increased serum PRL and decreased Pg and GH. In HT rats mammary DNA and protein tissue content was doubled. Receptor concentrations were expressed per mg DNA. Mammary PRL-R were increased in HT1 rats, while E-R and Pg-R were significantly lower in both HT groups. HT0.25 and HT1 rats had increased uterine E-R and Pg-R and decreased liver PRL-R and GH-R as well as their mRNAs. Liver E-R, PRL-R and GH-R were decreased in C21 rats, while uterine Pg-R were increased. Thus, some of the observed changes (serum Pg and GH, mammary and uterine Pg-R, and liver GH-R and PRL-R decreases and serum PRL increase) may be due at least partially to the advancement in luteolysis and delivery, being similar to the changes observed between days 20 and 21. The changes in serum B, mammary PRL-R, and mammary and uterine E-R may be caused solely by the T4 treatments and may play a role in the alterations previously observed.
Authors:
R R Rosato; H Jammes; G A Jahn
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Endocrine research     Volume:  24     ISSN:  0743-5800     ISO Abbreviation:  Endocr. Res.     Publication Date:  1998 May 
Date Detail:
Created Date:  1998-11-19     Completed Date:  1998-11-19     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8408548     Medline TA:  Endocr Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  269-84     Citation Subset:  IM    
Affiliation:
Laboratorio de Reproducción y Lactancia, CRICYT-CONICET, Mendoza, Argentina.
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MeSH Terms
Descriptor/Qualifier:
Animals
Corticosterone / blood
Cytosol / metabolism
DNA / analysis
Estradiol / blood
Female
Growth Hormone / blood
Hormones / blood*
Liver / drug effects*,  metabolism
Mammary Glands, Animal / drug effects*,  metabolism
Membrane Proteins / analysis
Pregnancy
Progesterone / blood
Prolactin / blood
Rats
Rats, Wistar
Receptors, Cell Surface / metabolism*
Receptors, Estradiol / metabolism
Receptors, Neuropeptide / genetics,  metabolism
Receptors, Progesterone / metabolism
Thyroxine / pharmacology*
Uterus / drug effects*,  metabolism
Chemical
Reg. No./Substance:
0/Hormones; 0/Membrane Proteins; 0/Receptors, Cell Surface; 0/Receptors, Estradiol; 0/Receptors, Neuropeptide; 0/Receptors, Progesterone; 50-22-6/Corticosterone; 50-28-2/Estradiol; 57-83-0/Progesterone; 7488-70-2/Thyroxine; 9002-62-4/Prolactin; 9002-72-6/Growth Hormone; 9007-49-2/DNA

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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