Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks

Maintaining the intrinsic excitability of neurons is crucial for stable brain activity. This can be achieved by the homeostatic regulation of membrane ion channel conductances, although it is not well understood how these processes influence broader aspects of neuron and network function. One of the...

Full description

Bibliographic Details
Main Author: Sweeney, Yann
Format: Doctoral Thesis
Language:English
Published: KTH, Beräkningsvetenskap och beräkningsteknik (CST) 2016
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-185747
http://nbn-resolving.de/urn:isbn:978-91-7595-970-2
id ndltd-UPSALLA1-oai-DiVA.org-kth-185747
record_format oai_dc
spelling ndltd-UPSALLA1-oai-DiVA.org-kth-1857472016-04-27T05:16:45ZFunctional Relevance of Homeostatic Intrinsic Plasticity in Neurons and NetworksengSweeney, YannKTH, Beräkningsvetenskap och beräkningsteknik (CST)School of Informatics, University of Edinburgh, UKStockholm2016Maintaining the intrinsic excitability of neurons is crucial for stable brain activity. This can be achieved by the homeostatic regulation of membrane ion channel conductances, although it is not well understood how these processes influence broader aspects of neuron and network function. One of the many mechanisms which contribute towards this task is the modulation of potassium channel conductances by activity-dependent nitric oxide signalling. Here, we first investigate this mechanism in a conductance-based neuron model. By fitting the model to experimental data we find that nitric oxide signalling improves synaptic transmission fidelity at high firing rates, but that there is an increase in the metabolic cost of action potentials associated with this improvement. Although the improvement in function had been observed previously in experiment, the metabolic constraint was unknown. This additional constraint provides a plausible explanation for the selective activation of nitric oxide signalling only at high firing rates. In addition to mediating homeostatic control of intrinsic excitability, nitric oxide can diffuse freely across cell membranes, providing a unique mechanism for neurons to communicate within a network, independent of synaptic connectivity. We next conduct a theoretical investigation of the distinguishing roles of diffusive homeostasis mediated by nitric oxide in comparison with canonical non-diffusive homeostasis in cortical networks. We find that both forms of homeostasis robustly maintain stable activity. However, the resulting networks differ, with diffusive homeostasis maintaining substantial heterogeneity in activity levels of individual neurons, a feature disrupted in networks with non-diffusive homeostasis. This results in networks capable of representing input heterogeneity, and linearly responding over a broader range of inputs than those undergoing non-diffusive homeostasis. We further show that diffusive homeostasis interferes less than non-diffusive homeostasis in the synaptic weight dynamics of networks undergoing Hebbian plasticity. Overall, these results suggest a novel homeostatic mechanism for maintaining stable network activity while simultaneously minimising metabolic cost and conserving network functionality. <p>Joint Doctoral Program in Neuroinformatics.  https://www.kth.se/eurospin</p><p>Public defence Monday, 23 May 2016, at 9.00 a.m. in Room 1,15, Meeting and Training suite, 1st Floor, Library, Univ Edinburgh, School of Informatics (can be joined via videoconference from Konstantinbågen, Drottning Kristinas väg 4, Kungliga Tekniska högskolan, Stockholm.</p><p>QC 20160426</p>Doctoral thesis, monographinfo:eu-repo/semantics/doctoralThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-185747urn:isbn:978-91-7595-970-2TRITA-CSC-A, 1653-5723 ; 2016:08application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Doctoral Thesis
sources NDLTD
description Maintaining the intrinsic excitability of neurons is crucial for stable brain activity. This can be achieved by the homeostatic regulation of membrane ion channel conductances, although it is not well understood how these processes influence broader aspects of neuron and network function. One of the many mechanisms which contribute towards this task is the modulation of potassium channel conductances by activity-dependent nitric oxide signalling. Here, we first investigate this mechanism in a conductance-based neuron model. By fitting the model to experimental data we find that nitric oxide signalling improves synaptic transmission fidelity at high firing rates, but that there is an increase in the metabolic cost of action potentials associated with this improvement. Although the improvement in function had been observed previously in experiment, the metabolic constraint was unknown. This additional constraint provides a plausible explanation for the selective activation of nitric oxide signalling only at high firing rates. In addition to mediating homeostatic control of intrinsic excitability, nitric oxide can diffuse freely across cell membranes, providing a unique mechanism for neurons to communicate within a network, independent of synaptic connectivity. We next conduct a theoretical investigation of the distinguishing roles of diffusive homeostasis mediated by nitric oxide in comparison with canonical non-diffusive homeostasis in cortical networks. We find that both forms of homeostasis robustly maintain stable activity. However, the resulting networks differ, with diffusive homeostasis maintaining substantial heterogeneity in activity levels of individual neurons, a feature disrupted in networks with non-diffusive homeostasis. This results in networks capable of representing input heterogeneity, and linearly responding over a broader range of inputs than those undergoing non-diffusive homeostasis. We further show that diffusive homeostasis interferes less than non-diffusive homeostasis in the synaptic weight dynamics of networks undergoing Hebbian plasticity. Overall, these results suggest a novel homeostatic mechanism for maintaining stable network activity while simultaneously minimising metabolic cost and conserving network functionality. === <p>Joint Doctoral Program in Neuroinformatics.  https://www.kth.se/eurospin</p><p>Public defence Monday, 23 May 2016, at 9.00 a.m. in Room 1,15, Meeting and Training suite, 1st Floor, Library, Univ Edinburgh, School of Informatics (can be joined via videoconference from Konstantinbågen, Drottning Kristinas väg 4, Kungliga Tekniska högskolan, Stockholm.</p><p>QC 20160426</p>
author Sweeney, Yann
spellingShingle Sweeney, Yann
Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
author_facet Sweeney, Yann
author_sort Sweeney, Yann
title Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
title_short Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
title_full Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
title_fullStr Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
title_full_unstemmed Functional Relevance of Homeostatic Intrinsic Plasticity in Neurons and Networks
title_sort functional relevance of homeostatic intrinsic plasticity in neurons and networks
publisher KTH, Beräkningsvetenskap och beräkningsteknik (CST)
publishDate 2016
url http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-185747
http://nbn-resolving.de/urn:isbn:978-91-7595-970-2
work_keys_str_mv AT sweeneyyann functionalrelevanceofhomeostaticintrinsicplasticityinneuronsandnetworks
_version_ 1718250732862308352