PMID- 26561607 OWN - NLM STAT- MEDLINE DCOM- 20161018 LR - 20181113 IS - 1522-1598 (Electronic) IS - 0022-3077 (Print) IS - 0022-3077 (Linking) VI - 115 IP - 1 DP - 2016 Jan 1 TI - Balanced ionotropic receptor dynamics support signal estimation via voltage-dependent membrane noise. PG - 530-45 LID - 10.1152/jn.00786.2015 [doi] AB - Encoding behaviorally relevant stimuli in a noisy background is critical for animals to survive in their natural environment. We identify core biophysical and synaptic mechanisms that permit the encoding of low-frequency signals in pyramidal neurons of the weakly electric fish Apteronotus leptorhynchus, an animal that can accurately encode even miniscule amplitude modulations of its self-generated electric field. We demonstrate that slow NMDA receptor (NMDA-R)-mediated excitatory postsynaptic potentials (EPSPs) are able to summate over many interspike intervals (ISIs) of the primary electrosensory afferents (EAs), effectively eliminating the baseline EA ISI correlations from the pyramidal cell input. Together with a dynamic balance of NMDA-R and GABA-A-R currents, this permits stimulus-evoked changes in EA spiking to be transmitted efficiently to target electrosensory lobe (ELL) pyramidal cells, for encoding low-frequency signals. Interestingly, AMPA-R activity is depressed and appears to play a negligible role in the generation of action potentials. Instead, we hypothesize that cell-intrinsic voltage-dependent membrane noise supports the encoding of perithreshold sensory input; this noise drives a significant proportion of pyramidal cell spikes. Together, these mechanisms may be sufficient for the ELL to encode signals near the threshold of behavioral detection. CI - Copyright (c) 2016 the American Physiological Society. FAU - Marcoux, Curtis M AU - Marcoux CM AD - Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; FAU - Clarke, Stephen E AU - Clarke SE AD - Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; FAU - Nesse, William H AU - Nesse WH AD - Department of Mathematics, University of Utah, Salt Lake City, Utah; FAU - Longtin, Andre AU - Longtin A AD - Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; Department of Physics, University of Ottawa, Ottawa, Ontario, Canada; and Brain and Mind Institute and Center for Neural Dynamics, University of Ottawa, Ottawa, Ontario, Canada. FAU - Maler, Leonard AU - Maler L AD - Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; Brain and Mind Institute and Center for Neural Dynamics, University of Ottawa, Ottawa, Ontario, Canada lmaler@uottawa.ca. LA - eng GR - 49510/Canadian Institutes of Health Research/Canada GR - 6027/Canadian Institutes of Health Research/Canada PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20151111 PL - United States TA - J Neurophysiol JT - Journal of neurophysiology JID - 0375404 RN - 0 (Receptors, AMPA) RN - 0 (Receptors, GABA) RN - 0 (Receptors, N-Methyl-D-Aspartate) SB - IM MH - Afferent Pathways/*physiology MH - Animals MH - Electric Fish MH - Electric Stimulation MH - Female MH - Male MH - Pyramidal Cells/*physiology MH - Receptors, AMPA/*physiology MH - Receptors, GABA/*physiology MH - Receptors, N-Methyl-D-Aspartate/*physiology MH - *Synaptic Potentials PMC - PMC4760475 OTO - NOTNLM OT - NMDA receptor OT - correlations OT - electric fish OT - signal detection OT - spike train OT - stochastic resonance EDAT- 2015/11/13 06:00 MHDA- 2016/10/19 06:00 PMCR- 2017/01/01 CRDT- 2015/11/13 06:00 PHST- 2015/08/10 00:00 [received] PHST- 2015/11/10 00:00 [accepted] PHST- 2015/11/13 06:00 [entrez] PHST- 2015/11/13 06:00 [pubmed] PHST- 2016/10/19 06:00 [medline] PHST- 2017/01/01 00:00 [pmc-release] AID - jn.00786.2015 [pii] AID - JN-00786-2015 [pii] AID - 10.1152/jn.00786.2015 [doi] PST - ppublish SO - J Neurophysiol. 2016 Jan 1;115(1):530-45. doi: 10.1152/jn.00786.2015. Epub 2015 Nov 11.