AJP - Endo Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 250: E121-E124, 1986;
0193-1849/86 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kakita, T.
Right arrow Articles by Odell, W. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kakita, T.
Right arrow Articles by Odell, W. D.

AJP - Endocrinology and Metabolism, Vol 250, Issue 2 121-E124, Copyright © 1986 by American Physiological Society


ARTICLES

Pituitary gland: one site of ultrashort-feedback regulation for control of thyrotropin

T. Kakita and W. D. Odell

Studies from our laboratory have previously demonstrated sensitive and specific autoregulatory control systems for thyrotropin (TSH), luteinizing hormone (LH), and follicle-stimulating hormone (FSH) in the rabbit. Because our studies of LH autoregulation showed the feedback regulation acted directly at a pituitary level, the current studies were designed to investigate whether the TSH control system also acted at the pituitary level. Two species-specific TSH assays were employed; a rabbit TSH radioimmunoassay which showed little or no reaction to human TSH, and a human TSH radioimmunoassay which showed little or no reaction to rabbit TSH. Both in vivo and in vitro studies were performed. TRH (thyrotropin-releasing hormone) in doses of 2, 10, and 50 micrograms was injected as an intravenous bolus into thyroidectomized hypothyroid rabbits during continuous perfusion with highly purified human TSH (hTSH) or with saline. In these in vivo studies, TRH-stimulated rabbit TSH (rTSH) secretion was suppressed by hTSH perfusion compared with control saline perfusion. The effect of hTSH was studied in vitro by employing short-term cultured rabbit pituitary cells. When hTSH was added to the incubation medium, TRH-stimulated rTSH secretion was inhibited. From these studies, we conclude that one site of the autoregulatory control for TSH in the rabbit is at the pituitary level. These studies do not exclude a possible additional short-loop feedback control at an hypothalamic level, but such a site of action is not required to explain the autoregulatory phenomenon.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online