The time pattern of glycinergic inhibitory postsynaptic currents (IPSCs) in sympathetic preganglionic neurons was studied in thin transverse spinal cord slices of neonatal (1-10 days postnatal) rats by means of the patch-clamp technique. Three time patterns could be distinguished: (i) large events [mostly > 400 pA (30-36 degrees C)] occurring at regular intervals, (ii) small events occurring at irregular intervals, and (iii) small events occurring in transient (1.5-10 s), high-frequency (> 15 Hz) bursts of synaptic activity. The large regular events had uniform kinetics which was consistent with the idea of a proximal site of origin for all of these events. They were reversibly inhibited in amplitude and frequency by extracellular application of a high concentration of acetylcholine (200 mu M) or the specific nicotinic acetylcholine receptor agonist dimethylphenylpiperazinium iodide (DMPP; 1 mM), but unaffected by glutamate (100 mu M). IPSCs occurring in bursts had slower and less uniform kinetics, suggesting a more diverse site of origin, The frequency of events decreased during a burst. Similar bursts could be induced by extracellular application of glutamate receptor agonists. These results indicate that sympathetic preganglionic neurons in a thin, transverse spinal cord slice receive at least two different glycinergic inputs.
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E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USAE Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
Antunes, VR
Brailoiu, GC
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E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USAE Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
Brailoiu, GC
Kwok, EH
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E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USAE Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
Kwok, EH
Scruggs, P
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E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USAE Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
Scruggs, P
Dun, NJ
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E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USAE Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
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FLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIAFLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIA
PILOWSKY, PM
LLEWELLYNSMITH, IJ
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FLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIAFLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIA
LLEWELLYNSMITH, IJ
MINSON, JB
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FLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIAFLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIA
MINSON, JB
ARNOLDA, LF
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FLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIAFLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIA
ARNOLDA, LF
CHALMERS, JP
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FLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIAFLINDERS UNIV S AUSTRALIA, FLINDERS MED CTR, CTR NEUROSCI, BEDFORD PK, SA 5042, AUSTRALIA