Modulation of dopamine receptors by thyrotropin-releasing hormone in the rat brain
Nanomolar concentration of thyrotropin-releasing hormone (TRH) in vitro caused a significant reduction of [ 3H]apomorphine binding sites (70% of the control) in the rat striatum and the limbic forebrain. [ 3H]Spiperone binding was not affected by TRH. On the other hand, dopamine and apomorphine disp...
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Published in | Peptides (New York, N.Y. : 1980) Vol. 8; no. 2; pp. 319 - 325 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.03.1987
Elsevier Science |
Subjects | |
Online Access | Get full text |
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Summary: | Nanomolar concentration of thyrotropin-releasing hormone (TRH)
in vitro caused a significant reduction of [
3H]apomorphine binding sites (70% of the control) in the rat striatum and the limbic forebrain. [
3H]Spiperone binding was not affected by TRH. On the other hand, dopamine and apomorphine displaced [
3H]TRH binding partially, suggesting the presence of a TRH receptor subpopulation that has a high affinity for dopamine agonist. Most of the neuroleptics displaced [
3H]TRH binding dose-dependently in the micromolar range. (−)-Sulpiride had no affinity to TRH receptors. These findings suggest that one of the important roles of TRH as a neuromodulator is to modulate receptors for classical neurotransmitters, and this receptor-receptor interaction may be of importance in explaining the well known stimulating effects of TRH on the dopaminergic system. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0196-9781 1873-5169 |
DOI: | 10.1016/0196-9781(87)90107-0 |