Inhibitory Transmission in Locus Coeruleus Neurons Expressing GABA A Receptor Epsilon Subunit Has a Number of Unique Properties
Fast inhibitory synaptic transmission in the brain relies on ionotropic GABA A receptors (GABA A R). Eighteen genes code for GABA A R subunits, but little is known about the ε subunit. Our aim was to identify the synaptic transmission properties displayed by native receptors incorporating ε. Immunog...
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Published in | Journal of neurophysiology Vol. 102; no. 4; pp. 2312 - 2325 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.10.2009
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Online Access | Get full text |
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Abstract | Fast inhibitory synaptic transmission in the brain relies on ionotropic GABA
A
receptors (GABA
A
R). Eighteen genes code for GABA
A
R subunits, but little is known about the ε subunit. Our aim was to identify the synaptic transmission properties displayed by native receptors incorporating ε. Immunogold localization detected ε at synaptic sites on locus coeruleus (LC) neurons. In situ hybridization revealed prominent signals from ε, and θ mRNAs, some low β1 and β3 signals, and no γ signal. Using in vivo extracellular and in vitro patch-clamp recordings in LC, we established that neuron firing rates, GABA-activated currents, and mIPSC charge were insensitive to the benzodiazepine flunitrazepam (FLU), in agreement with the characteristics of recombinant receptors including an ε subunit. Surprisingly, LC provided binding sites for benzodiazepines, and GABA-induced currents were potentiated by diazepam (DZP) in the micromolar range. A number of GABA
A
R ligands significantly potentiated GABA-induced currents, and zinc ions were only active at concentrations above 1 μM, further indicating that receptors were not composed of only α and β subunits, but included an ε subunit. In contrast to recombinant receptors including an ε subunit, GABA
A
R in LC showed no agonist-independent opening. Finally, we determined that mIPSCs, as well as ensemble currents induced by ultra-fast GABA application, exhibited surprisingly slow rise times. Our work thus defines the signature of native GABA
A
R with a subunit composition including ε: differential sensitivity to FLU and DZP and slow rise time of currents. We further propose that α
3,
β
1/3,
θ and ε subunits compose GABA
A
R in LC. |
---|---|
AbstractList | Fast inhibitory synaptic transmission in the brain relies on ionotropic GABA
A
receptors (GABA
A
R). Eighteen genes code for GABA
A
R subunits, but little is known about the ε subunit. Our aim was to identify the synaptic transmission properties displayed by native receptors incorporating ε. Immunogold localization detected ε at synaptic sites on locus coeruleus (LC) neurons. In situ hybridization revealed prominent signals from ε, and θ mRNAs, some low β1 and β3 signals, and no γ signal. Using in vivo extracellular and in vitro patch-clamp recordings in LC, we established that neuron firing rates, GABA-activated currents, and mIPSC charge were insensitive to the benzodiazepine flunitrazepam (FLU), in agreement with the characteristics of recombinant receptors including an ε subunit. Surprisingly, LC provided binding sites for benzodiazepines, and GABA-induced currents were potentiated by diazepam (DZP) in the micromolar range. A number of GABA
A
R ligands significantly potentiated GABA-induced currents, and zinc ions were only active at concentrations above 1 μM, further indicating that receptors were not composed of only α and β subunits, but included an ε subunit. In contrast to recombinant receptors including an ε subunit, GABA
A
R in LC showed no agonist-independent opening. Finally, we determined that mIPSCs, as well as ensemble currents induced by ultra-fast GABA application, exhibited surprisingly slow rise times. Our work thus defines the signature of native GABA
A
R with a subunit composition including ε: differential sensitivity to FLU and DZP and slow rise time of currents. We further propose that α
3,
β
1/3,
θ and ε subunits compose GABA
A
R in LC. |
Author | Boué-Grabot, E. Belujon, P. Batten, T.F.C. Baufreton, J. Garret, M. Ugedo, L. Grandoso, L. Taupignon, A. I. |
Author_xml | – sequence: 1 givenname: P. surname: Belujon fullname: Belujon, P. organization: University Bordeaux, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Bordeaux, France – sequence: 2 givenname: J. surname: Baufreton fullname: Baufreton, J. organization: University Bordeaux, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Bordeaux, France – sequence: 3 givenname: L. surname: Grandoso fullname: Grandoso, L. organization: Department of Pharmacology, School of Medicine, University of the Basque Country, Vizcaya, Spain; and – sequence: 4 givenname: E. surname: Boué-Grabot fullname: Boué-Grabot, E. organization: University Bordeaux, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Bordeaux, France – sequence: 5 givenname: T.F.C. surname: Batten fullname: Batten, T.F.C. organization: Leeds Institute of Genetics, Therapeutics and Health (LIGHT), University of Leeds, Leeds, United Kingdom – sequence: 6 givenname: L. surname: Ugedo fullname: Ugedo, L. organization: Department of Pharmacology, School of Medicine, University of the Basque Country, Vizcaya, Spain; and – sequence: 7 givenname: M. surname: Garret fullname: Garret, M. organization: University Bordeaux, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Bordeaux, France – sequence: 8 givenname: A. I. surname: Taupignon fullname: Taupignon, A. I. organization: University Bordeaux, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Bordeaux, France |
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receptors (GABA
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A
R subunits, but little is... |
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