Activation of group I metabotropic glutamate receptors induces long-term depression at sensory synapses in superficial spinal dorsal horn

被引:26
作者
Chen, J [1 ]
Heinke, B [1 ]
Sandkühler, J [1 ]
机构
[1] Univ Heidelberg, Inst Physiol & Pathophysiol, D-69120 Heidelberg, Germany
关键词
(S)-3,5-DHPG; (1S; 3R)-ACPD; A delta-fiber; pertussis toxin; phospholipase C; spinal cord slice; nociception;
D O I
10.1016/S0028-3908(00)00084-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Low-frequency stimulation of primary afferent A delta-fibers can induce long-term depression of synaptic transmission in rat, superficial spinal dorsal horn. Here, we have identified another form of long-term depression in superficial spinal dorsal horn neurons that is induced by specific group I but not group II metabotropic glutamate receptor (mGluR) agonists. Synaptic strength between A delta-fibers and dorsal horn neurons was examined by intracellular recordings in a spinal cord-dorsal root slice preparation from young rat. In the presence of bicuculline and strychnine, bath application of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1S,3R)-ACPD) or the specific group I mGluR agonist (S)-3.5-dihydroxyphenylycine ((S)-3,5-DHPG) but not the specific group II mGluR agonist (2S,2'R,3'R)-2-(2',3'-dicarboxycyclopropyl)glycine (DCG-IV) for 20 min produced an acute and a long-term depression of synaptic strength. Bath application of the N-methyl-D-aspartate receptor antagonist D-2-amino-5-phosphonovaleric acid did not affect these depressions by (1S,3R)-ACPD. After pre-incubation of slices with pertussis toxin, a G-protein inhibitor, (1S,3R)-ACPD still induced acute and long-term depressions. The phospholipase C inhibitor U73122 stereoselectively blocked the induction of long-term depression without affecting acute synaptic inhibition. This study demonstrates that, in the spinal cord, diner activation of group I mGluRs that are coupled to phospholipase C through pertussis toxin-insensitive G-proteins induces a longterm depression of synaptic strength. This may be relevant to the processing of sensory information in the spinal cord, including nociception. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2231 / 2243
页数:13
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