Expression of corticotropin releasing factor (CRF), urocortin and CRF type 1 receptors in hypothalamic-hypophyseal systems under osmotic stimulation

被引:34
作者
Imaki, T
Katsumata, H
Miyata, M
Naruse, M
Imaki, J
Minami, S
机构
[1] Nippon Med Sch, Inst Gerontol, Dept Bioregulat, Kawasaki, Kanagawa, Japan
[2] Tokyo Womens Med Univ, Dept Physiol, Tokyo, Japan
[3] Tokyo Womens Med Univ, Dept Med, Tokyo, Japan
[4] RIKEN, Brain Sci Inst, Lab Learning & Memory, Wako, Saitama 35101, Japan
[5] Nippon Med Sch, Dept Anat, Tokyo 113, Japan
关键词
CRF; CRF receptor; urocortin; magnocellular neurones; osmotic stimulation; oxytocin; vasopressin; pituitary gland;
D O I
10.1046/j.1365-2826.2001.00629.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The expression of corticotropin releasing factor (CRF) and urocortin in hypothalamic magnocellular neurones increases in response to osmotic challenge. To gain a better understanding of the physiological roles of CRF and urocortin in fluid homeostasis, CRF, urocortin and CRF type 1 receptor (CRFR-1) gene expression was examined in the hypothalamic-hypophyseal system usingin situ and double-label in situ hybridization following chronic salt loading. CRFR-1 expression was further examined by immunohistochemistry and receptor binding. Ingestion of hypertonic saline by Sprague-Dawley rats for 7 days induced CRF mRNA exclusively in the oxytocin neurones of the magnocellular paraventricular nucleus (PVN) and the supraoptic nucleus (SON), but induced CRFR-1 mRNA in both oxytocin and vasopressin-containing magnocellular neurones. Hypertonic saline treatment also increased urocortin mRNA expression in the PVN and the SON. In the SON, urocortin was localized to vasopressin and oxytocin neurones but was rarely seen in CRF-positive cells. Changes in CRFR-1 mRNA expression in magnocellular neurones by hypertonic saline treatment were accompanied by changes in CRFR-1 protein levels and receptor binding. Hypertonic saline treatment increased CRFR-1-like immunoreactivity in the magnocellular PVN and SON, and decreased it in the parvocellular PVN. CRF receptor binding in the PVN and SON was also increased in response to osmotic stimulation. Finally, hypertonic saline treatment increased CRFR-1 mRNA, CRFR-1-like immunoreactivity and CRF receptor binding in the intermediate pituitary. These results demonstrate that the increase in the expression of CRF and urocortin message in magnocellular neurones induced by salt loading is accompanied by an increase in CRF receptor levels and binding in the hypothalamus and intermediate pituitary. Thus, CRF and urocortin may exert modulatory effects locally within magnocellular neurones as well as at the pituitary gland in response to osmotic stimulation.
引用
收藏
页码:328 / 338
页数:11
相关论文
共 47 条
[1]   REGULATION OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS DURING WATER-DEPRIVATION [J].
AGUILERA, G ;
LIGHTMAN, SL ;
KISS, A .
ENDOCRINOLOGY, 1993, 132 (01) :241-248
[2]  
ALZEIN M, 1984, NEUROENDOCRINOL LETT, V6, P151
[4]   Vasopressin and oxytocin neurones of hypothalamic supraoptic and paraventricular nuclei co-express mRNA for type-1 andType-2 corticotropin-releasing hormone receptors [J].
Arima, H ;
Aguilera, G .
JOURNAL OF NEUROENDOCRINOLOGY, 2000, 12 (09) :833-842
[5]   RELEASE OF OXYTOCIN INDUCED BY SALT LOADING AND ITS INFLUENCE ON RENAL EXCRETION IN THE MALE-RAT [J].
BALMENT, RJ ;
BRIMBLE, MJ ;
FORSLING, ML .
JOURNAL OF PHYSIOLOGY-LONDON, 1980, 308 (NOV) :439-449
[6]   CORTICOTROPIN-RELEASING HORMONE STIMULATES NEUROHYPOPHYSEAL HORMONE-RELEASE THROUGH AN INTERACTION WITH THE INTERMEDIATE LOBE OF THE PITUITARY [J].
BONDY, CA ;
GAINER, H .
JOURNAL OF NEUROENDOCRINOLOGY, 1989, 1 (01) :5-8
[7]   CENTRAL ADMINISTRATION OF CORTICOTROPIN-RELEASING FACTOR MODULATES OXYTOCIN SECRETION IN THE RAT [J].
BRUHN, TO ;
SUTTON, SW ;
PLOTSKY, PM ;
VALE, WW .
ENDOCRINOLOGY, 1986, 119 (04) :1558-1563
[8]   IDENTIFICATION OF A 7 TRANSMEMBRANE HELIX RECEPTOR FOR CORTICOTROPIN-RELEASING FACTOR AND SAUVAGINE IN MAMMALIAN BRAIN [J].
CHANG, CP ;
PEARSE, RV ;
OCONNELL, S ;
ROSENFELD, MG .
NEURON, 1993, 11 (06) :1187-1195
[9]  
Chen JC, 2000, J COMP NEUROL, V420, P305, DOI 10.1002/(SICI)1096-9861(20000508)420:3<305::AID-CNE3>3.0.CO
[10]  
2-8