Postnatal Maturation of Rat Hypothalamoneurohypophysial Neurons: Evidence for a Developmental Decrease in Calcium Entry During Action Potentials
H. Widmer , H. Amerdeil , P. Fontanaud , and M. G. Desarménien Biologie des Neurones Endocrines, Centre National de la Recherche Scientifique Unité Propre de Recherche 9055, CCIPE, 34094 Montpellier Cedex 5, France Widmer, H., H. Amerdeil, P. Fontanaud, and M. G. Desarménien. Postnatal maturation of...
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description | H. Widmer ,
H. Amerdeil ,
P. Fontanaud , and
M. G. Desarménien
Biologie des Neurones Endocrines, Centre National de la Recherche Scientifique Unité Propre de Recherche 9055, CCIPE, 34094 Montpellier Cedex 5, France
Widmer, H., H. Amerdeil, P. Fontanaud, and M. G. Desarménien. Postnatal maturation of rat hypothalamoneurohypophysial neurons: evidence for a developmental decrease in calcium entry during action potentials. J. Neurophysiol. 77: 260-271, 1997. Action potentials and voltage-gated currents were studied in acutely dissociated neurosecretory cells from the rat supraoptic nucleus during the first three postnatal weeks (PW1-PW3), a period corresponding to the final establishment of neuroendocrine relationships. Action potential duration (at half maximum) decreased from 2.7 to 1.8 ms; this was attributable to a decrease in decay time. Application of cadmium (250 µM) reduced the decay time by 43% at PW1 and 21% at PW3, indicating that the contribution of calcium currents to action potentials decreased during postnatal development. The density of high-voltage-activated calcium currents increased from 4.4 to 10.1 pA/pF at postnatal days 1-5 and 11-14, respectively. The conductance density of sustained potassium current, measured at +20 mV, increased from 0.35 (PW1) to 0.53 (PW3) nS/pF. The time to half-maximal amplitude did not change. Conductance density and time- and voltage-dependent inactivation of the transient potassium current were stable from birth. At PW1, the density and time constant of decay (measured at 0 mV) were 0.29 nS/pF ( n = 12) and 17.9 ms ( n = 10), respectively. Voltage-dependent properties and density (1.1 nS/pF) of the sodium current did not change postnatally. During PW1, fitting the mean activation data with a Boltzmann function gave a half-activation potential of 25 mV. A double Boltzman equation was necessary to adequately fit the inactivation data, suggesting the presence of two populations of sodium channels. One population accounted for ~14% of the channels, with a half-inactivation potential of 86 mV; the remaining population showed a half-inactivation potential of 51 mV. A mathematical model, based on Hodgkin-Huxley equations, was used to assess the respective contributions of individual currents to the action potential. When the densities of calcium and sustained potassium currents were changed from immature to mature values, the decay time of the action potentials generated with the model decreased from 2.85 to 1.95 ms |
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H. Amerdeil ,
P. Fontanaud , and
M. G. Desarménien
Biologie des Neurones Endocrines, Centre National de la Recherche Scientifique Unité Propre de Recherche 9055, CCIPE, 34094 Montpellier Cedex 5, France
Widmer, H., H. Amerdeil, P. Fontanaud, and M. G. Desarménien. Postnatal maturation of rat hypothalamoneurohypophysial neurons: evidence for a developmental decrease in calcium entry during action potentials. J. Neurophysiol. 77: 260-271, 1997. Action potentials and voltage-gated currents were studied in acutely dissociated neurosecretory cells from the rat supraoptic nucleus during the first three postnatal weeks (PW1-PW3), a period corresponding to the final establishment of neuroendocrine relationships. Action potential duration (at half maximum) decreased from 2.7 to 1.8 ms; this was attributable to a decrease in decay time. Application of cadmium (250 µM) reduced the decay time by 43% at PW1 and 21% at PW3, indicating that the contribution of calcium currents to action potentials decreased during postnatal development. The density of high-voltage-activated calcium currents increased from 4.4 to 10.1 pA/pF at postnatal days 1-5 and 11-14, respectively. The conductance density of sustained potassium current, measured at +20 mV, increased from 0.35 (PW1) to 0.53 (PW3) nS/pF. The time to half-maximal amplitude did not change. Conductance density and time- and voltage-dependent inactivation of the transient potassium current were stable from birth. At PW1, the density and time constant of decay (measured at 0 mV) were 0.29 nS/pF ( n = 12) and 17.9 ms ( n = 10), respectively. Voltage-dependent properties and density (1.1 nS/pF) of the sodium current did not change postnatally. During PW1, fitting the mean activation data with a Boltzmann function gave a half-activation potential of 25 mV. A double Boltzman equation was necessary to adequately fit the inactivation data, suggesting the presence of two populations of sodium channels. One population accounted for ~14% of the channels, with a half-inactivation potential of 86 mV; the remaining population showed a half-inactivation potential of 51 mV. A mathematical model, based on Hodgkin-Huxley equations, was used to assess the respective contributions of individual currents to the action potential. When the densities of calcium and sustained potassium currents were changed from immature to mature values, the decay time of the action potentials generated with the model decreased from 2.85 to 1.95 ms. A similar reduction was obtained when only the density of the potassium current was increased. Integration of the calcium currents generated during mature and immature action potentials demonstrated a significant decrease in calcium entry during development. We conclude that the developmental reduction of the action potential duration 1 ) is a consequence of the developmentally regulated increase in a sustained potassium current and 2 ) leads to a reduction of the participation of calcium currents in the action potential, resulting in a decreased amount of calcium entering the cell during each action potential.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.1997.77.1.260</identifier><identifier>PMID: 9120568</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Action Potentials - physiology ; Animals ; Axons - physiology ; Calcium Channels - physiology ; Computer Simulation ; Electrophysiology ; Female ; Hypothalamo-Hypophyseal System - cytology ; Hypothalamo-Hypophyseal System - growth & development ; Ion Channel Gating - physiology ; Kinetics ; Male ; Membrane Potentials - physiology ; Models, Neurological ; Neurons - physiology ; Patch-Clamp Techniques ; Potassium Channels - physiology ; Rats ; Sodium Channels - physiology</subject><ispartof>Journal of neurophysiology, 1997-01, Vol.77 (1), p.260-271</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-3983c6577bda7c5db33fd1a461920850a004270866676c78bfcc0f5164fd50f63</citedby><cites>FETCH-LOGICAL-c399t-3983c6577bda7c5db33fd1a461920850a004270866676c78bfcc0f5164fd50f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9120568$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Widmer, H</creatorcontrib><creatorcontrib>Amerdeil, H</creatorcontrib><creatorcontrib>Fontanaud, P</creatorcontrib><creatorcontrib>Desarmenien, M. G</creatorcontrib><title>Postnatal Maturation of Rat Hypothalamoneurohypophysial Neurons: Evidence for a Developmental Decrease in Calcium Entry During Action Potentials</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>H. Widmer ,
H. Amerdeil ,
P. Fontanaud , and
M. G. Desarménien
Biologie des Neurones Endocrines, Centre National de la Recherche Scientifique Unité Propre de Recherche 9055, CCIPE, 34094 Montpellier Cedex 5, France
Widmer, H., H. Amerdeil, P. Fontanaud, and M. G. Desarménien. Postnatal maturation of rat hypothalamoneurohypophysial neurons: evidence for a developmental decrease in calcium entry during action potentials. J. Neurophysiol. 77: 260-271, 1997. Action potentials and voltage-gated currents were studied in acutely dissociated neurosecretory cells from the rat supraoptic nucleus during the first three postnatal weeks (PW1-PW3), a period corresponding to the final establishment of neuroendocrine relationships. Action potential duration (at half maximum) decreased from 2.7 to 1.8 ms; this was attributable to a decrease in decay time. Application of cadmium (250 µM) reduced the decay time by 43% at PW1 and 21% at PW3, indicating that the contribution of calcium currents to action potentials decreased during postnatal development. The density of high-voltage-activated calcium currents increased from 4.4 to 10.1 pA/pF at postnatal days 1-5 and 11-14, respectively. The conductance density of sustained potassium current, measured at +20 mV, increased from 0.35 (PW1) to 0.53 (PW3) nS/pF. The time to half-maximal amplitude did not change. Conductance density and time- and voltage-dependent inactivation of the transient potassium current were stable from birth. At PW1, the density and time constant of decay (measured at 0 mV) were 0.29 nS/pF ( n = 12) and 17.9 ms ( n = 10), respectively. Voltage-dependent properties and density (1.1 nS/pF) of the sodium current did not change postnatally. During PW1, fitting the mean activation data with a Boltzmann function gave a half-activation potential of 25 mV. A double Boltzman equation was necessary to adequately fit the inactivation data, suggesting the presence of two populations of sodium channels. One population accounted for ~14% of the channels, with a half-inactivation potential of 86 mV; the remaining population showed a half-inactivation potential of 51 mV. A mathematical model, based on Hodgkin-Huxley equations, was used to assess the respective contributions of individual currents to the action potential. When the densities of calcium and sustained potassium currents were changed from immature to mature values, the decay time of the action potentials generated with the model decreased from 2.85 to 1.95 ms. A similar reduction was obtained when only the density of the potassium current was increased. Integration of the calcium currents generated during mature and immature action potentials demonstrated a significant decrease in calcium entry during development. We conclude that the developmental reduction of the action potential duration 1 ) is a consequence of the developmentally regulated increase in a sustained potassium current and 2 ) leads to a reduction of the participation of calcium currents in the action potential, resulting in a decreased amount of calcium entering the cell during each action potential.</description><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Axons - physiology</subject><subject>Calcium Channels - physiology</subject><subject>Computer Simulation</subject><subject>Electrophysiology</subject><subject>Female</subject><subject>Hypothalamo-Hypophyseal System - cytology</subject><subject>Hypothalamo-Hypophyseal System - growth & development</subject><subject>Ion Channel Gating - physiology</subject><subject>Kinetics</subject><subject>Male</subject><subject>Membrane Potentials - physiology</subject><subject>Models, Neurological</subject><subject>Neurons - physiology</subject><subject>Patch-Clamp Techniques</subject><subject>Potassium Channels - physiology</subject><subject>Rats</subject><subject>Sodium Channels - physiology</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1vEzEQtRCohMKdC5JP3LId72ZtL7cqSWmlAhUqZ8vx2llHu_Ziewv5F_xknCaUCxKn-XrvzWgeQm8JFITU5cXOFaRpWMFYQYqSwjM0y-1yTuqGP0czgJxXwNhL9CrGHQCwGsozdNaQEmrKZ-jXnY_JySR7_EmmKchkvcPe4K8y4ev96FMnezl4p6fgu1yP3T7ajP58aLj4Aa8fbKud0tj4gCVe6Qfd-3HQ7qC50ipoGTW2Di9lr-w04LVLYY9XU7Buiy_V48I7nzIh68bX6IXJQb85xXP07Wp9v7ye3375eLO8vJ2rqmnSvGp4pWjN2KaVTNXtpqpMS-SCkqYEXoMEWJQMOKWUUcX4xigFpiZ0YdoaDK3O0fuj7hj890nHJAYble576bSfomCck6bi8F9gfnXJAUgGwhGogo8xaCPGYAcZ9oKAOLgldk4c3BKMCSKyW5ny7qQ9bQbdPhFO9uR5eZx3dtv9sEGLx_f73m_34mrq-3v9M2XZP4JibM3fg_9Fyic8bf8NedWyrA</recordid><startdate>19970101</startdate><enddate>19970101</enddate><creator>Widmer, H</creator><creator>Amerdeil, H</creator><creator>Fontanaud, P</creator><creator>Desarmenien, M. G</creator><general>Am Phys Soc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19970101</creationdate><title>Postnatal Maturation of Rat Hypothalamoneurohypophysial Neurons: Evidence for a Developmental Decrease in Calcium Entry During Action Potentials</title><author>Widmer, H ; Amerdeil, H ; Fontanaud, P ; Desarmenien, M. G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-3983c6577bda7c5db33fd1a461920850a004270866676c78bfcc0f5164fd50f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Axons - physiology</topic><topic>Calcium Channels - physiology</topic><topic>Computer Simulation</topic><topic>Electrophysiology</topic><topic>Female</topic><topic>Hypothalamo-Hypophyseal System - cytology</topic><topic>Hypothalamo-Hypophyseal System - growth & development</topic><topic>Ion Channel Gating - physiology</topic><topic>Kinetics</topic><topic>Male</topic><topic>Membrane Potentials - physiology</topic><topic>Models, Neurological</topic><topic>Neurons - physiology</topic><topic>Patch-Clamp Techniques</topic><topic>Potassium Channels - physiology</topic><topic>Rats</topic><topic>Sodium Channels - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Widmer, H</creatorcontrib><creatorcontrib>Amerdeil, H</creatorcontrib><creatorcontrib>Fontanaud, P</creatorcontrib><creatorcontrib>Desarmenien, M. G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Widmer, H</au><au>Amerdeil, H</au><au>Fontanaud, P</au><au>Desarmenien, M. G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Postnatal Maturation of Rat Hypothalamoneurohypophysial Neurons: Evidence for a Developmental Decrease in Calcium Entry During Action Potentials</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>1997-01-01</date><risdate>1997</risdate><volume>77</volume><issue>1</issue><spage>260</spage><epage>271</epage><pages>260-271</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>H. Widmer ,
H. Amerdeil ,
P. Fontanaud , and
M. G. Desarménien
Biologie des Neurones Endocrines, Centre National de la Recherche Scientifique Unité Propre de Recherche 9055, CCIPE, 34094 Montpellier Cedex 5, France
Widmer, H., H. Amerdeil, P. Fontanaud, and M. G. Desarménien. Postnatal maturation of rat hypothalamoneurohypophysial neurons: evidence for a developmental decrease in calcium entry during action potentials. J. Neurophysiol. 77: 260-271, 1997. Action potentials and voltage-gated currents were studied in acutely dissociated neurosecretory cells from the rat supraoptic nucleus during the first three postnatal weeks (PW1-PW3), a period corresponding to the final establishment of neuroendocrine relationships. Action potential duration (at half maximum) decreased from 2.7 to 1.8 ms; this was attributable to a decrease in decay time. Application of cadmium (250 µM) reduced the decay time by 43% at PW1 and 21% at PW3, indicating that the contribution of calcium currents to action potentials decreased during postnatal development. The density of high-voltage-activated calcium currents increased from 4.4 to 10.1 pA/pF at postnatal days 1-5 and 11-14, respectively. The conductance density of sustained potassium current, measured at +20 mV, increased from 0.35 (PW1) to 0.53 (PW3) nS/pF. The time to half-maximal amplitude did not change. Conductance density and time- and voltage-dependent inactivation of the transient potassium current were stable from birth. At PW1, the density and time constant of decay (measured at 0 mV) were 0.29 nS/pF ( n = 12) and 17.9 ms ( n = 10), respectively. Voltage-dependent properties and density (1.1 nS/pF) of the sodium current did not change postnatally. During PW1, fitting the mean activation data with a Boltzmann function gave a half-activation potential of 25 mV. A double Boltzman equation was necessary to adequately fit the inactivation data, suggesting the presence of two populations of sodium channels. One population accounted for ~14% of the channels, with a half-inactivation potential of 86 mV; the remaining population showed a half-inactivation potential of 51 mV. A mathematical model, based on Hodgkin-Huxley equations, was used to assess the respective contributions of individual currents to the action potential. When the densities of calcium and sustained potassium currents were changed from immature to mature values, the decay time of the action potentials generated with the model decreased from 2.85 to 1.95 ms. A similar reduction was obtained when only the density of the potassium current was increased. Integration of the calcium currents generated during mature and immature action potentials demonstrated a significant decrease in calcium entry during development. We conclude that the developmental reduction of the action potential duration 1 ) is a consequence of the developmentally regulated increase in a sustained potassium current and 2 ) leads to a reduction of the participation of calcium currents in the action potential, resulting in a decreased amount of calcium entering the cell during each action potential.</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>9120568</pmid><doi>10.1152/jn.1997.77.1.260</doi><tpages>12</tpages></addata></record> |
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subjects | Action Potentials - physiology Animals Axons - physiology Calcium Channels - physiology Computer Simulation Electrophysiology Female Hypothalamo-Hypophyseal System - cytology Hypothalamo-Hypophyseal System - growth & development Ion Channel Gating - physiology Kinetics Male Membrane Potentials - physiology Models, Neurological Neurons - physiology Patch-Clamp Techniques Potassium Channels - physiology Rats Sodium Channels - physiology |
title | Postnatal Maturation of Rat Hypothalamoneurohypophysial Neurons: Evidence for a Developmental Decrease in Calcium Entry During Action Potentials |
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