EXPRESSION OF ESTROGEN RECEPTOR-BETA MESSENGER-RIBONUCLEIC-ACID IN OXYTOCIN AND VASOPRESSIN NEURONS OF THE RAT SUPRAOPTIC AND PARAVENTRICULAR NUCLEI

Citation
E. Hrabovszky et al., EXPRESSION OF ESTROGEN RECEPTOR-BETA MESSENGER-RIBONUCLEIC-ACID IN OXYTOCIN AND VASOPRESSIN NEURONS OF THE RAT SUPRAOPTIC AND PARAVENTRICULAR NUCLEI, Endocrinology, 139(5), 1998, pp. 2600-2604
Citations number
30
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00137227
Volume
139
Issue
5
Year of publication
1998
Pages
2600 - 2604
Database
ISI
SICI code
0013-7227(1998)139:5<2600:EOERMI>2.0.ZU;2-7
Abstract
The regulatory actions of estrogen on magnocellular oxytocin (OT) and vasopressin (VP) neurons of the paraventricular (PVN) and supraoptic ( SON) nuclei are well documented. To date it is still debated whether t he effect of estrogens is exerted directly or mediated by estrogen-sen sitive interneurons. Previous immunocytochemical (ICC) and in situ hyb ridization (ISH) studies detected either law levels or absence of the classical estrogen receptor (ER-alpha) in the PVN and the SON of the r at. The present experiments using a combined ICC and ISH method were u ndertaken to examine the expression of the recently cloned beta form o f ER (ER-beta) in OT- and VP-immunoreactive (IR) neuronal systems of t he rat hypothalamus. The results demonstrate that the highest cellular levels of ER-beta messenger RNA (mRNA) in OT-IR neurons can be visual ized in the caudal portion of the PVN and in an area ventro-medial to the central core of TTP-ITC cells. These neurons were previously shown to project caudally to the brain stem and the spinal cord to regulate autonomic functions. in addition, the whole rostro-caudal extent of t he PVN and the SON contained OT-IR neurons that coexpressed variable l evels of ER-beta mRNA. Similarly, the presence of ER-beta mRNA was see n in a large population of VP-IR paraventricular and supraoptic newton s. In the SON, somewhat stronger hybridization signal was detected in VP-IR neurons as compared with OT-IR neurons. Together, these findings provide strong support for the concept that the functions of OT- and VP-IR neurons in the PVN and the SON are regulated directly by estroge n and that the genomic effects of estrogens are mediated by ER-beta.