Bistable dynamics underlying excitability of ion homeostasis in neuron models.
When neurons fire action potentials, dissipation of free energy is usually not directly considered, because the change in free energy is often negligible compared to the immense reservoir stored in neural transmembrane ion gradients and the long-term energy requirements are met through chemical ener...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2014-05-01
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| Series: | PLoS Computational Biology |
| Online Access: | http://europepmc.org/articles/PMC4006707?pdf=render |
| _version_ | 1811212977879121920 |
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| author | Niklas Hübel Eckehard Schöll Markus A Dahlem |
| author_facet | Niklas Hübel Eckehard Schöll Markus A Dahlem |
| author_sort | Niklas Hübel |
| collection | DOAJ |
| description | When neurons fire action potentials, dissipation of free energy is usually not directly considered, because the change in free energy is often negligible compared to the immense reservoir stored in neural transmembrane ion gradients and the long-term energy requirements are met through chemical energy, i.e., metabolism. However, these gradients can temporarily nearly vanish in neurological diseases, such as migraine and stroke, and in traumatic brain injury from concussions to severe injuries. We study biophysical neuron models based on the Hodgkin-Huxley (HH) formalism extended to include time-dependent ion concentrations inside and outside the cell and metabolic energy-driven pumps. We reveal the basic mechanism of a state of free energy-starvation (FES) with bifurcation analyses showing that ion dynamics is for a large range of pump rates bistable without contact to an ion bath. This is interpreted as a threshold reduction of a new fundamental mechanism of ionic excitability that causes a long-lasting but transient FES as observed in pathological states. We can in particular conclude that a coupling of extracellular ion concentrations to a large glial-vascular bath can take a role as an inhibitory mechanism crucial in ion homeostasis, while the Na⁺/K⁺ pumps alone are insufficient to recover from FES. Our results provide the missing link between the HH formalism and activator-inhibitor models that have been successfully used for modeling migraine phenotypes, and therefore will allow us to validate the hypothesis that migraine symptoms are explained by disturbed function in ion channel subunits, Na⁺/K⁺ pumps, and other proteins that regulate ion homeostasis. |
| first_indexed | 2024-04-12T05:38:29Z |
| format | Article |
| id | doaj.art-18ba59a75d9b4a9e91998e42bf39cbcb |
| institution | Directory Open Access Journal |
| issn | 1553-734X 1553-7358 |
| language | English |
| last_indexed | 2024-04-12T05:38:29Z |
| publishDate | 2014-05-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS Computational Biology |
| spelling | doaj.art-18ba59a75d9b4a9e91998e42bf39cbcb2022-12-22T03:45:43ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582014-05-01105e100355110.1371/journal.pcbi.1003551Bistable dynamics underlying excitability of ion homeostasis in neuron models.Niklas HübelEckehard SchöllMarkus A DahlemWhen neurons fire action potentials, dissipation of free energy is usually not directly considered, because the change in free energy is often negligible compared to the immense reservoir stored in neural transmembrane ion gradients and the long-term energy requirements are met through chemical energy, i.e., metabolism. However, these gradients can temporarily nearly vanish in neurological diseases, such as migraine and stroke, and in traumatic brain injury from concussions to severe injuries. We study biophysical neuron models based on the Hodgkin-Huxley (HH) formalism extended to include time-dependent ion concentrations inside and outside the cell and metabolic energy-driven pumps. We reveal the basic mechanism of a state of free energy-starvation (FES) with bifurcation analyses showing that ion dynamics is for a large range of pump rates bistable without contact to an ion bath. This is interpreted as a threshold reduction of a new fundamental mechanism of ionic excitability that causes a long-lasting but transient FES as observed in pathological states. We can in particular conclude that a coupling of extracellular ion concentrations to a large glial-vascular bath can take a role as an inhibitory mechanism crucial in ion homeostasis, while the Na⁺/K⁺ pumps alone are insufficient to recover from FES. Our results provide the missing link between the HH formalism and activator-inhibitor models that have been successfully used for modeling migraine phenotypes, and therefore will allow us to validate the hypothesis that migraine symptoms are explained by disturbed function in ion channel subunits, Na⁺/K⁺ pumps, and other proteins that regulate ion homeostasis.http://europepmc.org/articles/PMC4006707?pdf=render |
| spellingShingle | Niklas Hübel Eckehard Schöll Markus A Dahlem Bistable dynamics underlying excitability of ion homeostasis in neuron models. PLoS Computational Biology |
| title | Bistable dynamics underlying excitability of ion homeostasis in neuron models. |
| title_full | Bistable dynamics underlying excitability of ion homeostasis in neuron models. |
| title_fullStr | Bistable dynamics underlying excitability of ion homeostasis in neuron models. |
| title_full_unstemmed | Bistable dynamics underlying excitability of ion homeostasis in neuron models. |
| title_short | Bistable dynamics underlying excitability of ion homeostasis in neuron models. |
| title_sort | bistable dynamics underlying excitability of ion homeostasis in neuron models |
| url | http://europepmc.org/articles/PMC4006707?pdf=render |
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