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Endocrinology, doi:10.1210/en.2007-1378
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Endocrinology Vol. 149, No. 3 1389-1398
Copyright © 2008 by The Endocrine Society

Corticotropin-Releasing Hormone (CRH) Depresses N-Methyl-D-Aspartate Receptor-Mediated Current in Cultured Rat Hippocampal Neurons via CRH Receptor Type 1

Hui Sheng1, Yanmin Zhang1, Jihu Sun, Lu Gao, Bei Ma, Jianqiang Lu and Xin Ni

Department of Physiology (H.S., Y.Z., J.S., L.G., B.M., X.N.), Changhai Hospital (J.L.), The Key Laboratory of Molecular Neurobiology (H.S., Y.Z., J.S., L.G., B.M., X.N.), Ministry of Education, The Second Military Medical University, Shanghai 200433; and School of Kinesiology (J.L.), Shanghai University of Sport, 650 Qing Yuan Huan Road, Shanghai 200438, People’s Republic of China

Address all correspondence and requests for reprints to: Dr. Xin Ni, Department of Physiology, Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, People’s Republic of China. E-mail: nxljq2003{at}yahoo.com.cn.

CRH, the primary regulator of the neuroendocrine responses to stress, has been shown to modulate synaptic efficacy and the process of learning and memory in hippocampus. However, effects of CRH on N-methyl-D-aspartate (NMDA) receptor, the key receptor for synaptic plasticity, remain unclear. In primary cultured hippocampal neurons, using the technique of whole-cell patch-clamp recordings, we found that CRH (1 pmol/liter to 10 nmol/liter) inhibited NMDA-induced currents in a dose-dependent manner. This effect was reversed by the CRH receptor type 1 (CRHR1) antagonist antalarmin but not by the CRHR2 antagonist astressin-2B, suggesting that CRHR1 mediated the inhibitory effect of CRH. Investigations on the signaling pathways of CRH showed that CRH dose-dependently induced phosphorylated phospholipase C (PLC)-β3 expression and increased intracellular cAMP content in these cells. Blocking PLC activity with U73122 prevented CRH-induced depression of NMDA current, whereas blocking protein kinase A (H89) and adenylate cyclase (SQ22536) failed to affect the CRH-induced depression of NMDA current. Application of inositol-1,4,5-triphosphate receptor (IP3R) antagonist, Ca2+ chelators or protein kinase C (PKC) inhibitors also mainly blocked CRH-induced depression of NMDA currents, suggesting involvement of PLC/IP3R/Ca2+and PLC/PKC signaling pathways in CRH down-regulation of NMDA receptors. Our results suggest that CRH may exert neuromodulatory actions on hippocampus through regulating NMDA receptor function.




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Am. J. Physiol. Endocrinol. Metab.Home page
H. Sheng, T. Sun, B. Cong, P. He, Y. Zhang, J. Yan, C. Lu, and X. Ni
Corticotropin-releasing hormone stimulates SGK-1 kinase expression in cultured hippocampal neurons via CRH-R1
Am J Physiol Endocrinol Metab, October 1, 2008; 295(4): E938 - E946.
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