Functional properties of ionotropic glutamate receptor channels in rat sacral dorsal commissural neurons

Citation
Tl. Xu et al., Functional properties of ionotropic glutamate receptor channels in rat sacral dorsal commissural neurons, NEUROPHARM, 38(5), 1999, pp. 659-670
Citations number
51
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROPHARMACOLOGY
ISSN journal
00283908 → ACNP
Volume
38
Issue
5
Year of publication
1999
Pages
659 - 670
Database
ISI
SICI code
0028-3908(199905)38:5<659:FPOIGR>2.0.ZU;2-O
Abstract
Nystatin perforated patch and conventional whole-cell recording configurati ons were used to characterize the properties of ionotropic glutamate recept or (GluR) channels in neurons freshly dissociated from the rat sacral dorsa l commissural nucleus (SDCN). L-Glutamate (Glu), N-methyl-D-aspartate (NMDA ), quisqualate (QA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate ( AMPA) and kainate (KA) applied via a Y-tube produced inward currents at -44 mV which increased in a concentration-dependent manner; they desensitized when induced at higher concentrations except for the KA-induced current (I- KA). (1S-3R)1-amino-cyclopentane-1,3-dicarboxylate (1S-3R-ACPD) evoked no r esponse. The EC50 and Hill coefficient (n(H)) values of the GluR responses were 3.3 x 10(-5) M, 0.74 for Glu; 9.0 x 10(-5) M, 0.83 for NMDA; 6.4 x 10( -7) M, 1.30 for QA; 1.3 x 10(-4) M, 1.10 for AMPA and 9.6 x 10(-5) M. 1.30 for KA, respectively. The reversal potentials of the GluR responses were al l near 0 mV. The 6-Cyano-7-nitroquinoxaline-2-3-dione (CNQX) and D-2-amino- 5-phosphonovalerate (D-APV) suppressed the non-NMDA and NMDA responses in a concentration-dependent manner, respectively. Cyclothiazide strongly poten tiated both KA- and AMPA-induced responses while concanavalin A potentiated both the responses to a much lesser degree. NS-102 produced no significant effect on either KA- or AMPA-activated currents, while GYKI 52466 reversib ly blocked both the currents. The Ca2+ permeabilities (P-Ca/P-Cs) of the NM DA and AMPA receptor channels were 8.33 and 1.23, respectively. Tn addition , the current-voltage (I-V) relationship of I-KA showed little rectificatio n. There was a poor correlation between the Ca2+ permeability and the shape of the I-V curves of I,. These results suggest that rat SDCN neurons posse ss NMDA and non-NMDA receptor channels, and express AMPA type receptors wit h unique properties (slow desensitization to AMPA, high Ca2+ permeability b ut lack of inward rectification). These ionotropic receptor charnels may pl ay important roles in mediating and regulating pelvic visceral information including nociception. (C) 1999 Elsevier Science Ltd. All rights reserved.