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Distinct receptors underlie glutamatergic signalling in inspiratory rhythm‐generating networks and motor output pathways in neonatal rat
Author(s) -
Ireland M. F.,
Lenal F. C.,
Lorier A. R.,
Loomes D. E.,
Adachi T.,
Alvares T. S.,
Greer J. J.,
Funk G. D.
Publication year - 2008
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2007.150532
Subject(s) - kainate receptor , ampa receptor , glutamatergic , neuroscience , receptor , glutamate receptor , nmda receptor , cnqx , long term depression , silent synapse , biology , kainic acid , neurotransmission , chemistry , biochemistry
Despite the enormous diversity of glutamate (Glu) receptors and advances in understanding recombinant receptors, native Glu receptors underlying functionally identified inputs in active systems are poorly defined in comparison. In the present study we use UBP‐302, which antagonizes GluR5 subunit‐containing kainate (KA) receptors at ≤ 10 μ m , but other KA and AMPA receptors at ≥ 100 μ m , and rhythmically active in vitro preparations of neonatal rat to explore the contribution of non‐NMDA receptor signalling in rhythm‐generating and motor output compartments of the inspiratory network. At 10 μ m , UBP‐302 had no effect on inspiratory burst frequency or amplitude. At 100 μ m , burst amplitude recorded from XII, C1 and C4 nerve roots was significantly reduced, but frequency was unaffected. The lack of a frequency effect was confirmed when local application of UBP‐302 (100 μ m ) into the pre‐Bötzinger complex (preBötC) did not affect frequency but substance P evoked a 2‐fold increase. A UBP‐302‐sensitive (10 μ m ), ATPA‐evoked frequency increase, however, established that preBötC networks are sensitive to GluR5 activation. Whole‐cell recordings demonstrated that XII motoneurons also express functional GluR5‐containing KA receptors that do not contribute to inspiratory drive, and confirmed the dose dependence of UBP‐302 actions on KA and AMPA receptors. Our data provide the first evidence that the non‐NMDA (most probably AMPA) receptors mediating glutamatergic transmission within preBötC inspiratory rhythm‐generating networks are pharmacologically distinct from those transmitting drive to inspiratory motoneurons. This differential expression may ultimately be exploited pharmacologically to separately counteract depression of central respiratory rhythmogenesis or manipulate the drive to motoneurons controlling airway and pump musculature.