Characterization of GABA(A) and glycine receptors in neurons of the developing 
rat inferior colliculus

Kraushaar, U.; Backus, K. H.

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Characterization of GABA(A) and glycine receptors in neurons of the developing rat inferior colliculus

MPS-Authors

/persons/resource/persons207883

Backus, K. H.
Neuroanatomy Department, Max Planck Institute for Brain Research, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Kraushaar, U., & Backus, K. H. (2002). Characterization of GABA(A) and glycine receptors in neurons of the developing rat inferior colliculus. Pflügers Archiv: European Journal of Physiology, 445(2), 279-288.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002E-1FA5-7

Abstract

GABA(A) receptors (GABA(A)Rs) and glycine receptors (GlyRs) expressed in developing neurons (P3-8) of the rat inferior colliculus (IQ were investigated using fast application of transmitters on nucleated patches and whole-cell patch-clamp recordings. At a holding potential of -60 mV and an E-CI close to 0 mV GABA and glycine activated inward currents with a half- maximal activation concentration of 127 muM and 353 muM, respectively. GABAARs activated and deactivated significantly faster than GlyRs (20-80% rise-time: 0.71 ms for GABA(A)Rs and 1.31 ms for GlyRs; amplitude-weighted decay time constant, tau(W), 22.4+/-1.3 ms for GABA(A)Rs and 108.7+/-32.9 ms for GlyRs). The tau(W) values for receptor desensitization were 26.8+/-1.9 ms for GABA(A)Rs and 177.9+/-47.2 ms for GlyRs. Recovery from desensitization was significantly faster for GlyRs (tau=334 ms) than for GABA(A)Rs (tau(1)=82 ms; tau(2)=3783 ms). The tau(W) values of GABA(A)R-mediated spontaneous and miniature inhibitory postsynaptic currents were not significantly different from those of GABAARs activated by fast application, but significantly different to the tau(W) of GlyRs activated by fast application. The different properties of GABAARs and GlyRs expressed in the same IC neuron suggest a distinct functional contribution to the development of inhibitory synapses in the IC.