Metabotropic glutamate receptor antagonists, like GABA(B) antagonists, potentiate dorsal root-evoked excitatory synaptic transmission at neonatal rat spinal motoneurons in vitro

Recordings of whole-cell synaptic current responses elicited by electrical stimulation of dorsal roots were made from motoneurons, identified by antidromic invasion, in isolated spinal cord preparations from five- to eight-day-old Wistar rats. Supramaximal electrical stimulation of the dorsal root evoked complex excitatory postsynaptic currents with mean latencies (±S.E.M.) of 6.1±0.26 ms, peak amplitude of −650±47 pA and duration of 4.30±0.46 s ( n =34). All phases of excitatory postsynaptic currents were potentiated to approximately 20% above control levels in the presence of the metabotropic glutamate receptor antagonists S -2-amino-2-methyl-4-phosphonobutanoate (MAP4; 200 μ M; n =15) and 2 S ,1′ S ,2′ S -2-methyl-2-(carboxycyclopropyl)glycine (MCCG; 200 μ M; n =9). A similar level of potentiation was produced by the GABA B receptor antagonist 3- N [1-( S )-(3,4-dichlorophenyl)ethyl]amino-2-( S )-hydroxypropyl- P -benzyl-phosphinic acid (CGP55845; 200 nM; n =5). MAP4 (200 μ M) produced a six-fold rightward shift in the concentration–effect plot for the depressant action of the metabotropic glutamate receptor agonist S -2-amino-4-phosphonobutanoate ( L -AP4), whereas CGP55845 produced no significant change in the potency of l -AP4. MAP4 did not antagonize the depressant actions of baclofen ( n =8), 1 S ,3 S -1-aminocyclopentane-1,3-dicarboxylate ( n =4) or 2 S , 1′ S , 2′ S -2-(carboxycyclopropyle) glycine ( n =4). The metabotropic glutamate receptor antagonists produced no change in the holding current of any of the neurons, indicating that they had no significant postsynaptic excitatory actions. These results are the first to indicate a possible physiological role for metabotropic glutamate receptors in the spinal cord. Like GABA B receptors, they control glutamatergic synaptic transmission in the segmental spinal pathway to motoneurons. This is likely to be a presynaptic control mechanism.