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The Journal of Neurophysiology Vol. 88 No. 2 August 2002, pp. 847-860
Copyright ©2002 by the American Physiological Society
Department of Biology, University of Utah, Salt Lake City, Utah 84112
Rohrbough, Jeffrey and
Kendal Broadie.
Electrophysiological Analysis of Synaptic Transmission in Central
Neurons of Drosophila Larvae. J. Neurophysiol. 88: 847-860, 2002. We report functional
neuronal and synaptic transmission properties in Drosophila
CNS neurons. Whole cell current- and voltage-clamp recordings were made
from dorsally positioned neurons in the larval ventral nerve cord.
Comparison of neuronal Green Fluorescent Protein markers and
intracellular dye labeling revealed that recorded cells consisted
primarily of identified motor neurons. Neurons had resting potentials
of
50 to
60 mV and fired repetitive action potentials (APs) in
response to depolarizing current injection. Acetylcholine application
elicited large excitatory responses and AP bursts that were reversibly
blocked by the nicotinic receptor antagonist D-tubocurarine
(dtC). GABA and glutamate application elicited similar inhibitory
responses that reversed near normal resting potential and were
reversibly blocked by the chloride channel blocker picrotoxin. Multiple
types of endogenous synaptically driven activity were present in most
neurons, including fast spontaneous synaptic events resembling unitary
excitatory postsynaptic currents (EPSCs) and sustained excitatory
currents and potentials. Sustained forms of endogenous activity ranged
in amplitude from smaller subthreshold "intermediate" sustained
events to large "rhythmic" events that supported bursts of APs.
Electrical stimulation of peripheral nerves or focal stimulation of the
neuropil evoked sustained responses and fast EPSCs similar to
endogenous events. Endogenous activity and evoked responses required
external Ca2+ and were reversibly blocked by dtC
application, indicating that cholinergic synaptic transmission directly
underlies observed activity. Synaptic current amplitude and frequency
were reduced in shibire conditional dynamin mutants and
increased in dunce cAMP phosphodiesterase mutants. These
results complement and advance those of recent functional studies in
Drosophila embryonic neurons and demonstrate the feasibility
of in-depth synaptic transmission and plasticity studies in the
Drosophila CNS.
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