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The Journal of Neuroscience, February 15, 2003, 23(4):1441
Phase Resetting Light Pulses Induce Per1 and
Persistent Spike Activity in a Subpopulation of Biological Clock
Neurons
Sandra J.
Kuhlman1,
Rae
Silver2, 3,
Joseph
Le
Sauter2,
Abel
Bult-Ito4, and
Douglas G.
McMahon1
1 Department of Physiology, University of Kentucky,
Lexington, Kentucky 40536-0084, 2 Department of Psychology,
Barnard College, New York, New York 10027, 3 Departments of
Psychology, and Anatomy and Cell Biology, Columbia University, New
York, New York 10027, and 4 Institute of Arctic Biology,
University of Alaska Fairbanks, Fairbanks, Alaska 99775-7000
The endogenous circadian clock of the mammalian suprachiasmatic
nucleus (SCN) can be reset by light to synchronize the biological clock
of the brain with the external environment. This process involves induction of immediate-early genes such as the circadian clock
gene Period1 (Per1) and results in a
stable shift in the timing of behavioral and physiological rhythms on
subsequent days. The mechanisms by which gene activation permanently
alters the phase of clock neuron activity are unknown. To study the
relationship between acute gene activation and persistent changes in
the neurophysiology of SCN neurons, we recorded from SCN neurons marked
with a dynamic green fluorescent protein (GFP) reporter of
Per1 gene activity. Phase-resetting light pulses
resulted in Per1 induction in a distinct subset of SCN
neurons that also exhibited a persistent increase in action potential
frequency 3-5 hr after a light pulse. By simultaneously quantifying
Per1 gene activation and spike frequency in individual neurons, we found that the degree of Per1 induction was
highly correlated with neuronal spike frequency on a cell-by-cell
basis. Increased neuronal activity was mediated by membrane potential depolarization as a result of a reduction in outward potassium current.
Double-label immunocytochemistry revealed that vasoactive intestinal
peptide (VIP)-expressing cells, but not arginine vasopressin (AVP)-expressing cells, exhibited significant Per1
induction by light pulses. Rhythmic GFP expression occurred in both VIP
and AVP neurons. Our results indicate that the steps that link acute molecular events to permanent changes in clock phase involve persistent suppression of potassium current, downstream of Per1
gene induction, in a specific subset of Per1-expressing
neurons enriched for VIP.
Key words:
suprachiasmatic nucleus; circadian rhythms; GFP; transgenic mice; electrophysiology; gene expression; transcription
factors; potassium channels; vasoactive intestinal peptide; arginine
vasopressin; entrainment
Copyright © 2003 Society for Neuroscience 0270-6474/03/2341441-10$05.00/0
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