Details

Autor(en) / Beteiligte

• Lamsa, Karri
• Taira, Tomi

Titel

Use-Dependent Shift From Inhibitory to Excitatory GABAA Receptor Action in SP-O Interneurons in the Rat Hippocampal CA3 Area

Ist Teil von

• Journal of neurophysiology, 2003-09, Vol.90 (3), p.1983-1995

Ort / Verlag

United States: Am Phys Soc

Erscheinungsjahr

2003

Quelle

MEDLINE

Beschreibungen/Notizen

• Department of Biosciences, Division of Animal Physiology and Institute of Biotechnology, FIN-00014 University of Helsinki, Finland Submitted 22 January 2003; accepted in final form 12 May 2003 Cortical inhibitory interneurons set the pace of synchronous neuronal oscillations implicated in synaptic plasticity and various cognitive functions. The hyperpolarizing nature of inhibitory postsynaptic potentials (IPSPs) in interneurons has been considered crucial for the generation of oscillations at (15–30 Hz) and (30–100 Hz) frequency. Hippocampal basket cells and axo-axonic cells in stratum pyramidale-oriens (S-PO) play a central role in the synchronization of the local interneuronal network as well as in pacing of glutamatergic principal cell firing. A lack of conventional forms of plasticity in excitatory synapses onto interneurons facilitates their function as stable neuronal oscillators. We have used gramicidin-perforated and whole cell clamp recordings to study properties of GABA A R-mediated transmission in CA3 SP-O interneurons and in CA3 pyramidal cells in rat hippocampal slices during electrical 5- to 100-Hz stimulation and during spontaneous activity. We show that GABAergic synapses onto SP-O interneurons can easily switch their mode from inhibitory to excitatory during heightened activity. This is based on a depolarizing shift in the GABA A reversal potential ( E GABA-A ), which is much faster and more pronounced in interneurons than in pyramidal cells. We also found that the shift in interneuronal function was frequency dependent, being most prominent at 20- to 40-Hz activation of the GABAergic synapses. After 40-Hz tetanic stimulation (100 pulses), GABA A responses remained depolarizing for 45 s in the interneurons, promoting bursting in the GABAergic network. Hyperpolarizing E GABA-A was restored >60 s after the stimulus train. Similar but spontaneous GABAergic bursting was induced by application of 4-aminopyridine (100 µM) to slices. A shift to depolarizing IPSPs by the GABA A R permeant weak acid anion formate provoked interneuronal population bursting, supporting the role of GABAergic excitation in burst generation. Furthermore, depolarizing GABAergic potentials and synchronous interneuronal bursting were enhanced by pentobarbital (100 µM), a positive allosteric modulator of GABA A Rs, and were blocked by picrotoxin (100 µM). Intriguingly, GABAergic bursts displayed short (<1 s) oscillations at 15–40 Hz, even though only depolarizing GABA A responses were seen in the SP-O interneurons. This - rhythmicity in the interneuron network was dependent on electrotonic coupling, and was abolished by blockade of gap junctions with carbenoxolone (200 µM). Results here implicate the rapid activity-dependent degradation of hyperpolarizing IPSPs in SP-O interneurons in setting the temporal limits for a given interneuron to participate in - oscillations synchronized by GABAergic synapses. Furthermore, they imply that mutual GABAergic excitation provided by interneurons may be an integral part in the function of neuronal networks. We suggest that the use-dependent change in E GABA-A could represent a form of short-term plasticity in interneurons promoting coherent and sustained activation of local GABAergic networks. Present address and address for reprint requests: K. Lamsa, Dept. of Clinical and Experimental Epilepsy, Institute of Neurology, UCL, London WC1N 3BG, United Kingdom (E-mail: k.lamsa{at}ion.ucl.ac.uk ).