Enhancement of GABAA receptor-mediated conductances induced by nerve injury in a subclass of sensory neurons
A. A. Oyelese, D. L. Eng, G. B. Richerson and J. D. Kocsis Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA. 1. The effects of axotomy on the electrophysiologic properties of adult rat dorsal root ganglion (DRG) neurons were studied to understand the cha...
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creator | Oyelese, A. A Eng, D. L Richerson, G. B Kocsis, J. D |
description | A. A. Oyelese, D. L. Eng, G. B. Richerson and J. D. Kocsis
Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
1. The effects of axotomy on the electrophysiologic properties of adult rat
dorsal root ganglion (DRG) neurons were studied to understand the changes
in excitability induced by traumatic nerve injury. Nerve injury was induced
in vivo by sciatic nerve ligation with distal nerve transection. Two to
four weeks after nerve ligation, a time when a neuroma forms, lumbar (L4
and L5) DRG neurons were removed and placed in short-term tissue culture.
Whole cell patch-clamp recordings were made 5-24 h after plating. 2. DRG
neurons were grouped into large (43-65 microns)-, medium (34-42 microns)-,
and small (20-32 microns)- sized classes. Large neurons had short duration
action potentials with approximately 60% having inflections on the falling
phase of their action potentials. In contrast, action potentials of medium
and small neurons were longer in duration and approximately 68% had
inflections. 3. Pressure microejection of gamma-aminobutyric acid (GABA,
100 microM) or muscimol (100 microM) onto voltage-clamped DRG neurons
elicited a rapidly desensitizing inward current that was blocked by 200
microM bicuculline. To measure the peak conductance induced by GABA or
muscimol, neurons were voltage-clamped at a holding potential of -60 mV,
and pulses to -80 mV and -100 mV were applied at a rate of 2.5 or 5 Hz
during drug application. Slope conductances were calculated from plots of
whole cell current measured at each of these potentials. 4. GABA-induced
currents and conductances of control DRG neurons increased progressively
with cell diameter. The mean GABA conductance was 36 +/- 10 nS (mean +/-
SE) in small neurons, 124 +/- 21 nS in medium neurons, and 527 +/- 65 nS in
large neurons. 5. After axotomy, medium neurons had significantly larger
GABA-induced conductances compared with medium control neurons (390 +/- 50
vs. 124 +/- 21; P < 0.001). The increase in GABA conductance of medium
neurons was associated with a decrease in duration of action potentials. In
contrast, small neurons had no change in GABA conductance or action
potential duration after ligation. The GABA conductance of large control
neurons was highly variable, and ligation resulted in an increase that was
significant only for neurons > 50 microns. The mean action potential
duration in large neurons was not significantly changed, but neurons with
inflec |
doi_str_mv | 10.1152/jn.1995.74.2.673 |
format | Article |
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Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
1. The effects of axotomy on the electrophysiologic properties of adult rat
dorsal root ganglion (DRG) neurons were studied to understand the changes
in excitability induced by traumatic nerve injury. Nerve injury was induced
in vivo by sciatic nerve ligation with distal nerve transection. Two to
four weeks after nerve ligation, a time when a neuroma forms, lumbar (L4
and L5) DRG neurons were removed and placed in short-term tissue culture.
Whole cell patch-clamp recordings were made 5-24 h after plating. 2. DRG
neurons were grouped into large (43-65 microns)-, medium (34-42 microns)-,
and small (20-32 microns)- sized classes. Large neurons had short duration
action potentials with approximately 60% having inflections on the falling
phase of their action potentials. In contrast, action potentials of medium
and small neurons were longer in duration and approximately 68% had
inflections. 3. Pressure microejection of gamma-aminobutyric acid (GABA,
100 microM) or muscimol (100 microM) onto voltage-clamped DRG neurons
elicited a rapidly desensitizing inward current that was blocked by 200
microM bicuculline. To measure the peak conductance induced by GABA or
muscimol, neurons were voltage-clamped at a holding potential of -60 mV,
and pulses to -80 mV and -100 mV were applied at a rate of 2.5 or 5 Hz
during drug application. Slope conductances were calculated from plots of
whole cell current measured at each of these potentials. 4. GABA-induced
currents and conductances of control DRG neurons increased progressively
with cell diameter. The mean GABA conductance was 36 +/- 10 nS (mean +/-
SE) in small neurons, 124 +/- 21 nS in medium neurons, and 527 +/- 65 nS in
large neurons. 5. After axotomy, medium neurons had significantly larger
GABA-induced conductances compared with medium control neurons (390 +/- 50
vs. 124 +/- 21; P < 0.001). The increase in GABA conductance of medium
neurons was associated with a decrease in duration of action potentials. In
contrast, small neurons had no change in GABA conductance or action
potential duration after ligation. The GABA conductance of large control
neurons was highly variable, and ligation resulted in an increase that was
significant only for neurons > 50 microns. The mean action potential
duration in large neurons was not significantly changed, but neurons with
inflections on the falling phase of the action potential were less common
after ligation. There was no difference in resting potential or input
resistance between control and ligated groups, except that the resting
potential was less negative in small cells after axotomy.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.1995.74.2.673</identifier><identifier>PMID: 7472373</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Animals ; Axons - physiology ; gamma-Aminobutyric Acid - pharmacology ; Ganglia, Sensory - physiology ; Ganglia, Spinal - physiology ; Ion Channels - physiology ; Membrane Potentials - physiology ; Nerve Fibers - physiology ; Rats ; Rats, Wistar ; Receptors, GABA-A - drug effects ; Receptors, GABA-A - physiology ; Sciatic Nerve - physiology ; Time Factors</subject><ispartof>Journal of neurophysiology, 1995-08, Vol.74 (2), p.673-683</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2693-89dfadc5b4427038a6e914d4293ae3ae67234db770322d21fdb8e57f92a65cb93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7472373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oyelese, A. A</creatorcontrib><creatorcontrib>Eng, D. L</creatorcontrib><creatorcontrib>Richerson, G. B</creatorcontrib><creatorcontrib>Kocsis, J. D</creatorcontrib><title>Enhancement of GABAA receptor-mediated conductances induced by nerve injury in a subclass of sensory neurons</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>A. A. Oyelese, D. L. Eng, G. B. Richerson and J. D. Kocsis
Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
1. The effects of axotomy on the electrophysiologic properties of adult rat
dorsal root ganglion (DRG) neurons were studied to understand the changes
in excitability induced by traumatic nerve injury. Nerve injury was induced
in vivo by sciatic nerve ligation with distal nerve transection. Two to
four weeks after nerve ligation, a time when a neuroma forms, lumbar (L4
and L5) DRG neurons were removed and placed in short-term tissue culture.
Whole cell patch-clamp recordings were made 5-24 h after plating. 2. DRG
neurons were grouped into large (43-65 microns)-, medium (34-42 microns)-,
and small (20-32 microns)- sized classes. Large neurons had short duration
action potentials with approximately 60% having inflections on the falling
phase of their action potentials. In contrast, action potentials of medium
and small neurons were longer in duration and approximately 68% had
inflections. 3. Pressure microejection of gamma-aminobutyric acid (GABA,
100 microM) or muscimol (100 microM) onto voltage-clamped DRG neurons
elicited a rapidly desensitizing inward current that was blocked by 200
microM bicuculline. To measure the peak conductance induced by GABA or
muscimol, neurons were voltage-clamped at a holding potential of -60 mV,
and pulses to -80 mV and -100 mV were applied at a rate of 2.5 or 5 Hz
during drug application. Slope conductances were calculated from plots of
whole cell current measured at each of these potentials. 4. GABA-induced
currents and conductances of control DRG neurons increased progressively
with cell diameter. The mean GABA conductance was 36 +/- 10 nS (mean +/-
SE) in small neurons, 124 +/- 21 nS in medium neurons, and 527 +/- 65 nS in
large neurons. 5. After axotomy, medium neurons had significantly larger
GABA-induced conductances compared with medium control neurons (390 +/- 50
vs. 124 +/- 21; P < 0.001). The increase in GABA conductance of medium
neurons was associated with a decrease in duration of action potentials. In
contrast, small neurons had no change in GABA conductance or action
potential duration after ligation. The GABA conductance of large control
neurons was highly variable, and ligation resulted in an increase that was
significant only for neurons > 50 microns. The mean action potential
duration in large neurons was not significantly changed, but neurons with
inflections on the falling phase of the action potential were less common
after ligation. There was no difference in resting potential or input
resistance between control and ligated groups, except that the resting
potential was less negative in small cells after axotomy.</description><subject>Animals</subject><subject>Axons - physiology</subject><subject>gamma-Aminobutyric Acid - pharmacology</subject><subject>Ganglia, Sensory - physiology</subject><subject>Ganglia, Spinal - physiology</subject><subject>Ion Channels - physiology</subject><subject>Membrane Potentials - physiology</subject><subject>Nerve Fibers - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, GABA-A - drug effects</subject><subject>Receptors, GABA-A - physiology</subject><subject>Sciatic Nerve - physiology</subject><subject>Time Factors</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1r3DAQFaUl3aa991LwqTc7sj6s1aWwDWkaCPTSnoUsjddavNJWshP87yuRZdvCwAxv3ryZ4SH0scVN23Jyc_BNKyVvBGtI0wn6Cm0yTOqWy-1rtME41xQL8Ra9S-mAMRYckyt0JZggVNANmu78qL2BI_i5CkN1v_u621URDJzmEOsjWKdnsJUJ3i5mLtRUuVJnsF8rD_EJMnBY4ppTpau09GbSKRW1BD6FWFhLDD69R28GPSX4cM7X6Ne3u5-33-vHH_cPt7vH2pBO0nor7aCt4T1jRGC61R3IlllGJNWQo8u3M9uL3CPEknaw_Ra4GCTRHTe9pNfoy4vuaenzByb_FvWkTtEddVxV0E793_FuVPvwpEiHOeVF4PNZIIbfC6RZHV0yME3aQ1iSEoJ3THaFiF-IJoaUIgyXJS1WxSF18Ko4pARTRGWH8sinf4-7DJwt-bt7dPvx2UVQp3FNLkxhvxa1i9AfYBKcnA</recordid><startdate>19950801</startdate><enddate>19950801</enddate><creator>Oyelese, A. A</creator><creator>Eng, D. L</creator><creator>Richerson, G. B</creator><creator>Kocsis, J. D</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19950801</creationdate><title>Enhancement of GABAA receptor-mediated conductances induced by nerve injury in a subclass of sensory neurons</title><author>Oyelese, A. A ; Eng, D. L ; Richerson, G. B ; Kocsis, J. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2693-89dfadc5b4427038a6e914d4293ae3ae67234db770322d21fdb8e57f92a65cb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Axons - physiology</topic><topic>gamma-Aminobutyric Acid - pharmacology</topic><topic>Ganglia, Sensory - physiology</topic><topic>Ganglia, Spinal - physiology</topic><topic>Ion Channels - physiology</topic><topic>Membrane Potentials - physiology</topic><topic>Nerve Fibers - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, GABA-A - drug effects</topic><topic>Receptors, GABA-A - physiology</topic><topic>Sciatic Nerve - physiology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oyelese, A. A</creatorcontrib><creatorcontrib>Eng, D. L</creatorcontrib><creatorcontrib>Richerson, G. B</creatorcontrib><creatorcontrib>Kocsis, J. D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oyelese, A. A</au><au>Eng, D. L</au><au>Richerson, G. B</au><au>Kocsis, J. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancement of GABAA receptor-mediated conductances induced by nerve injury in a subclass of sensory neurons</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>1995-08-01</date><risdate>1995</risdate><volume>74</volume><issue>2</issue><spage>673</spage><epage>683</epage><pages>673-683</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>A. A. Oyelese, D. L. Eng, G. B. Richerson and J. D. Kocsis
Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
1. The effects of axotomy on the electrophysiologic properties of adult rat
dorsal root ganglion (DRG) neurons were studied to understand the changes
in excitability induced by traumatic nerve injury. Nerve injury was induced
in vivo by sciatic nerve ligation with distal nerve transection. Two to
four weeks after nerve ligation, a time when a neuroma forms, lumbar (L4
and L5) DRG neurons were removed and placed in short-term tissue culture.
Whole cell patch-clamp recordings were made 5-24 h after plating. 2. DRG
neurons were grouped into large (43-65 microns)-, medium (34-42 microns)-,
and small (20-32 microns)- sized classes. Large neurons had short duration
action potentials with approximately 60% having inflections on the falling
phase of their action potentials. In contrast, action potentials of medium
and small neurons were longer in duration and approximately 68% had
inflections. 3. Pressure microejection of gamma-aminobutyric acid (GABA,
100 microM) or muscimol (100 microM) onto voltage-clamped DRG neurons
elicited a rapidly desensitizing inward current that was blocked by 200
microM bicuculline. To measure the peak conductance induced by GABA or
muscimol, neurons were voltage-clamped at a holding potential of -60 mV,
and pulses to -80 mV and -100 mV were applied at a rate of 2.5 or 5 Hz
during drug application. Slope conductances were calculated from plots of
whole cell current measured at each of these potentials. 4. GABA-induced
currents and conductances of control DRG neurons increased progressively
with cell diameter. The mean GABA conductance was 36 +/- 10 nS (mean +/-
SE) in small neurons, 124 +/- 21 nS in medium neurons, and 527 +/- 65 nS in
large neurons. 5. After axotomy, medium neurons had significantly larger
GABA-induced conductances compared with medium control neurons (390 +/- 50
vs. 124 +/- 21; P < 0.001). The increase in GABA conductance of medium
neurons was associated with a decrease in duration of action potentials. In
contrast, small neurons had no change in GABA conductance or action
potential duration after ligation. The GABA conductance of large control
neurons was highly variable, and ligation resulted in an increase that was
significant only for neurons > 50 microns. The mean action potential
duration in large neurons was not significantly changed, but neurons with
inflections on the falling phase of the action potential were less common
after ligation. There was no difference in resting potential or input
resistance between control and ligated groups, except that the resting
potential was less negative in small cells after axotomy.</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>7472373</pmid><doi>10.1152/jn.1995.74.2.673</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | Animals Axons - physiology gamma-Aminobutyric Acid - pharmacology Ganglia, Sensory - physiology Ganglia, Spinal - physiology Ion Channels - physiology Membrane Potentials - physiology Nerve Fibers - physiology Rats Rats, Wistar Receptors, GABA-A - drug effects Receptors, GABA-A - physiology Sciatic Nerve - physiology Time Factors |
title | Enhancement of GABAA receptor-mediated conductances induced by nerve injury in a subclass of sensory neurons |
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