Corticotrophin-releasing hormone decreases synaptic transmission in rat sensorimotor cortex in vivo

被引:6
作者
Froc, DJ
Christie, BR
机构
[1] Univ British Columbia, Dept Psychol, Neurosci Program, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 1Z4, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
neocortex; plasticity; hormones; LTP; LTD; stress;
D O I
10.1016/j.neuroscience.2005.05.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Corticotrophin-releasing hormone is a key regulator of the mammalian stress response. Although its actions on behavior are well documented, the actions of corticotrophin-releasing hormone in cortical neuronal systems are poorly understood. In the present experiments, adult male Sprague-Dawley rats were anesthetized and field excitatory post-synaptic potential recordings were made from sensorimotor cortex layer II/III and layer V cells. Infusions of corticotrophin-releasing hormone (100 ng/nl) directly into the sensorimotor cortex produced a significant depression of the initial excitatory component of evoked responses that could be prevented by prior administration of a corticotrophin-releasing hormone antagonist. Although requiring the activation of corticotrophin-releasing hormone receptors, the depression was also dependent upon N-methyl-D-aspartate receptor activity and could be blocked by the competitive N-methyl-D-aspartate antagonist -3-(2-carboxypiperazin-4-yl)propyl-1-phosphonate. These findings demonstrate that corticotrophin-releasing hormone has a novel depressant-like action in sensorimotor cortex in vivo that may play a role in modulating motor activity during periods of stress. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:965 / 973
页数:9
相关论文
共 56 条
[1]   EFFECTS OF THE NMDA RECEPTOR CHANNEL ANTAGONISTS CPP AND MK801 ON HIPPOCAMPAL FIELD POTENTIALS AND LONG-TERM POTENTIATION IN ANESTHETIZED RATS [J].
ABRAHAM, WC ;
MASON, SE .
BRAIN RESEARCH, 1988, 462 (01) :40-46
[2]   CORTICOTROPIN RELEASING-FACTOR DECREASES POSTBURST HYPERPOLARIZATIONS AND EXCITES HIPPOCAMPAL-NEURONS [J].
ALDENHOFF, JB ;
GRUOL, DL ;
RIVIER, J ;
VALE, W ;
SIGGINS, GR .
SCIENCE, 1983, 221 (4613) :875-877
[3]  
Blank T, 2002, J NEUROSCI, V22, P3788
[4]   Corticotropin-releasing hormone (CRH) downregulates the function of its receptor (CRF1) and induces CRF1 expression in hippocampal and cortical regions of the immature rat brain [J].
Brunson, KL ;
Grigoriadis, DE ;
Lorang, MT ;
Baram, TZ .
EXPERIMENTAL NEUROLOGY, 2002, 176 (01) :75-86
[5]   Electrophysiological evidence against a neurotransmitter role of corticotropin-releasing hormone (CRH) in primary somatosensory cortex [J].
Cahusac, PMB ;
Castro, MG ;
Robertson, L ;
Lowenstein, PR .
BRAIN RESEARCH, 1998, 793 (1-2) :73-78
[6]  
Castro-Alamancos MA, 2002, J NEUROSCI, V22, P9651
[7]   Cortical sensory suppression during arousal is due to the activity-dependent depression of thalamocortical synapses [J].
Castro-Alamancos, MA ;
Oldford, E .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 541 (01) :319-331
[8]  
CASTROALAMANCOS MA, 1995, J NEUROSCI, V15, P5324
[9]  
CHALMERS DT, 1995, J NEUROSCI, V15, P6340
[10]   Changes in field potentials and membrane currents in rat sensorimotor cortex following repeated tetanization of the corpus callosum in vivo [J].
Chapman, CA ;
Trepel, C ;
Ivanco, TL ;
Froc, DJ ;
Wilson, K ;
Racine, RJ .
CEREBRAL CORTEX, 1998, 8 (08) :730-742