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J Appl Physiol 89: 1919-1927, 2000;
8750-7587/00 $5.00
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Vol. 89, Issue 5, 1919-1927, November 2000

State influences on ventral medullary surface and physiological responses to sodium cyanide challenges

Paul M. Macey1, Christopher A. Richard1,2, David M. Rector3, Rebecca K. Harper1, and Ronald M. Harper1

1 Department of Neurobiology and the Brain Research Institute, University of California at Los Angeles, Los Angeles, 90095-1763; 2 Department of Neurology, Sleep Disorders Center, University of California Irvine Medical Center, Orange, California 92868; and 3 Biophysics Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545

Intravenous sodium cyanide (NaCN) administration lowers ventral medullary surface (VMS) activity in anesthetized cats. Sleep states modify spontaneous and blood pressure-evoked VMS activity and may alter VMS responses to chemoreceptor input. We studied VMS activation during peripheral chemoreceptor stimulation by intravenous NaCN using optical procedures in six cats instrumented for recording sleep physiology during sham saline and control site trials. Images of scattered 660-nm light were collected at 50 frames/s with an optical device after 80-100 µg total bolus intravenous NaCN delivery during waking and sleep states. Cyanide elicited an initial ventilatory decline, followed by large inspiratory efforts and an increase in respiratory rate, except in rapid eye movement sleep, in which an initial breathing increase occurred. NaCN evoked a pronounced decrease in VMS activity in all states; control sites and sham injections showed little effect. The activity decline was faster in rapid eye movement sleep, and the activity nadir occurred later in waking. Sleep states alter the time course but not the extent of decline in VMS activity.

hypoxia; peripheral chemoreceptors; optical imaging; sleep; respiration


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L. A. Henderson, P. L. Yu, R. C. Frysinger, J.-P. Galons, R. Bandler, and R. M. Harper
Neural responses to intravenous serotonin revealed by functional magnetic resonance imaging
J Appl Physiol, January 1, 2002; 92(1): 331 - 342.
[Abstract] [Full Text] [PDF]




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