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J Neurophysiol 99: 976-988, 2008. First published December 12, 2007; doi:10.1152/jn.00930.2007
0022-3077/08 $8.00
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Circadian- and Light-Dependent Regulation of Resting Membrane Potential and Spontaneous Action Potential Firing of Drosophila Circadian Pacemaker Neurons

Vasu Sheeba1,*, Huaiyu Gu2,*, Vijay K. Sharma1,3, Diane K. O'Dowd2 and Todd C. Holmes1

1Department of Physiology and Biophysics and 2Department of Anatomy and Neurobiology, University of California, Irvine, California; and 3Evolutionary and Organismal Biology Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India

Submitted 17 August 2007; accepted in final form 11 December 2007

The ventral lateral neurons (LNvs) of adult Drosophila brain express oscillating clock proteins and regulate circadian behavior. Whole cell current-clamp recordings of large LNvs in freshly dissected Drosophila whole brain preparations reveal two spontaneous activity patterns that correlate with two underlying patterns of oscillating membrane potential: tonic and burst firing of sodium-dependent action potentials. Resting membrane potential and spontaneous action potential firing are rapidly and reversibly regulated by acute changes in light intensity. The LNv electrophysiological light response is attenuated, but not abolished, in cryb mutant flies hypomorphic for the cell-autonomous light-sensing protein CRYPTOCHROME. The electrical activity of the large LNv is circadian regulated, as shown by significantly higher resting membrane potential and frequency of spontaneous action potential firing rate and burst firing pattern during circadian subjective day relative to subjective night. The circadian regulation of membrane potential, spontaneous action potential firing frequency, and pattern of Drosophila large LNvs closely resemble mammalian circadian neuron electrical characteristics, suggesting a general evolutionary conservation of both physiological and molecular oscillator mechanisms in pacemaker neurons.


Address for reprint requests and other correspondence: T. C. Holmes, Department of Physiology and Biophysics, 340D Medical Sciences I, University of California, Irvine, Irvine, CA 92697 (E-mail: tholmes{at}uci.edu)




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