Cell-type specificity of mGluR activation in striatal neuronal subtypes

被引:25
作者
Pisani, A
Bernardi, G
Bonsi, P
Centonze, D
Giacomini, P
Calabresi, P
机构
[1] Univ Roma Tor Vergata, Dipartimento Neurosci, Neurol Clin, I-00133 Rome, Italy
[2] IRCCS Osped S Lucia, Rome, Italy
[3] Univ La Sapienza, Neurol Clin 2, Rome, Italy
关键词
amino acids; striatum; electrophysiology; metabotropic glutamate receptors; excitotoxicity;
D O I
10.1007/s007260070040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of metabotropic glutamate receptor (mGluR) activation were studied in medium spiny neurons and large aspiny (LA) interneurons by means of electrophysiological and optical recordings. DCG-IV and L-SOP, agonists for group II and III mGluRs, respectively, produced a presynaptic inhibitory effect on corticostriatal glutamatergic excitatory postsynaptic potentials (EPSPs) in both spiny and LA cells. Activation of group I mGluRs by the selective agonist 3,5-DHPG produced no effect on membrane properties and glutamatergic transmission in spiny neurons, whereas it did cause a membrane depolarization in LA interneurons coupled to increased input resistance. In combined optical and electrophysiological experiments, in spiny neurons 3,5-DHPG enhanced membrane depolarization and intracellular calcium (Ca2+) levels induced by NMDA applications, but not in LA interneurons. These data suggest the existence of a positive interaction between NMDA and group I mGlu receptors only in medium spiny cells which might, at least partially, account for the differential vulnerability to excitotoxic damage observed in striatal neuronal subtypes.
引用
收藏
页码:119 / 129
页数:11
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