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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Veröffentlicht in:Journal of neurophysiology 1995-08, Vol.74 (2), p.673-683
Hauptverfasser: Oyelese, A. A, Eng, D. L, Richerson, G. B, Kocsis, J. D
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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
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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. 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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. 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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 &lt; 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 &gt; 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. 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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 &lt; 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 &gt; 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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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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