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The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness
The conventional interpretation of spikes is from the perspective of an external observer with knowledge of a neuron’s inputs and outputs who is ignorant of the contents of the “black box” that is the neuron. Here we consider a neuron to be an observer and we interpret spikes from the neuron’s persp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010728/ https://www.ncbi.nlm.nih.gov/pubmed/24808854 http://dx.doi.org/10.3389/fncom.2014.00049 |
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author | Fiorillo, Christopher D. Kim, Jaekyung K. Hong, Su Z. |
author_facet | Fiorillo, Christopher D. Kim, Jaekyung K. Hong, Su Z. |
author_sort | Fiorillo, Christopher D. |
collection | PubMed |
description | The conventional interpretation of spikes is from the perspective of an external observer with knowledge of a neuron’s inputs and outputs who is ignorant of the contents of the “black box” that is the neuron. Here we consider a neuron to be an observer and we interpret spikes from the neuron’s perspective. We propose both a descriptive hypothesis based on physics and logic, and a prescriptive hypothesis based on biological optimality. Our descriptive hypothesis is that a neuron’s membrane excitability is “known” and the amplitude of a future excitatory postsynaptic conductance (EPSG) is “unknown”. Therefore excitability is an expectation of EPSG amplitude and a spike is generated only when EPSG amplitude exceeds its expectation (“prediction error”). Our prescriptive hypothesis is that a diversity of synaptic inputs and voltage-regulated ion channels implement “predictive homeostasis”, working to insure that the expectation is accurate. The homeostatic ideal and optimal expectation would be achieved when an EPSP reaches precisely to spike threshold, so that spike output is exquisitely sensitive to small variations in EPSG input. To an external observer who knows neither EPSG amplitude nor membrane excitability, spikes would appear random if the neuron is making accurate predictions. We review experimental evidence that spike probabilities are indeed maintained near an average of 0.5 under natural conditions, and we suggest that the same principles may also explain why synaptic vesicle release appears to be “stochastic”. Whereas the present hypothesis accords with principles of efficient coding dating back to Barlow (1961), it contradicts decades of assertions that neural activity is substantially “random” or “noisy”. The apparent randomness is by design, and like many other examples of apparent randomness, it corresponds to the ignorance of external macroscopic observers about the detailed inner workings of a microscopic system. |
format | Online Article Text |
id | pubmed-4010728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40107282014-05-07 The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness Fiorillo, Christopher D. Kim, Jaekyung K. Hong, Su Z. Front Comput Neurosci Neuroscience The conventional interpretation of spikes is from the perspective of an external observer with knowledge of a neuron’s inputs and outputs who is ignorant of the contents of the “black box” that is the neuron. Here we consider a neuron to be an observer and we interpret spikes from the neuron’s perspective. We propose both a descriptive hypothesis based on physics and logic, and a prescriptive hypothesis based on biological optimality. Our descriptive hypothesis is that a neuron’s membrane excitability is “known” and the amplitude of a future excitatory postsynaptic conductance (EPSG) is “unknown”. Therefore excitability is an expectation of EPSG amplitude and a spike is generated only when EPSG amplitude exceeds its expectation (“prediction error”). Our prescriptive hypothesis is that a diversity of synaptic inputs and voltage-regulated ion channels implement “predictive homeostasis”, working to insure that the expectation is accurate. The homeostatic ideal and optimal expectation would be achieved when an EPSP reaches precisely to spike threshold, so that spike output is exquisitely sensitive to small variations in EPSG input. To an external observer who knows neither EPSG amplitude nor membrane excitability, spikes would appear random if the neuron is making accurate predictions. We review experimental evidence that spike probabilities are indeed maintained near an average of 0.5 under natural conditions, and we suggest that the same principles may also explain why synaptic vesicle release appears to be “stochastic”. Whereas the present hypothesis accords with principles of efficient coding dating back to Barlow (1961), it contradicts decades of assertions that neural activity is substantially “random” or “noisy”. The apparent randomness is by design, and like many other examples of apparent randomness, it corresponds to the ignorance of external macroscopic observers about the detailed inner workings of a microscopic system. Frontiers Media S.A. 2014-04-29 /pmc/articles/PMC4010728/ /pubmed/24808854 http://dx.doi.org/10.3389/fncom.2014.00049 Text en Copyright © 2014 Fiorillo, Kim and Hong. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Fiorillo, Christopher D. Kim, Jaekyung K. Hong, Su Z. The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title | The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title_full | The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title_fullStr | The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title_full_unstemmed | The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title_short | The meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
title_sort | meaning of spikes from the neuron’s point of view: predictive homeostasis generates the appearance of randomness |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010728/ https://www.ncbi.nlm.nih.gov/pubmed/24808854 http://dx.doi.org/10.3389/fncom.2014.00049 |
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