Journal of Neuroscience, Vol 4, 897-907, Copyright © 1984 by Society for Neuroscience
Hypothalamic neurons responding to hemodynamic input and to stimulation in the pons may influence adrenocorticotropin release
DE Carlson, A Dornhorst, JW Maran and DS Gann
Experiments were designed to identify hemodynamically sensitive neurons in
the mediodorsal hypothalamus and to determine if they were also sensitive
to electrical stimulation of areas in the dorsal rostral pons that were
implicated previously in the control of adrenocorticotropin (ACTH) release.
Cats were anesthetized with chloralose and urethane, immobilized with
gallamine, and artificially respired. Hemodynamic stimuli included
constriction (CC) of the supradiaphragmatic inferior vena cava to reduce
venous return and sinusoidal volume pulsation (RA) of the right atrium (1
ml peak at 1 Hz). Previously, CC was shown to facilitate and RA was shown
to inhibit ACTH release. Electrical stimulation in the pons consisted of
single shocks (500 microA DC, 0.05 msec, negative-to-tip) delivered on each
of an array of three or four bipolar co-axial electrodes in the pons.
Twenty-three neurons were tested with only RA. Of these, two were
inhibited, two were facilitated, and 19 did not respond. Thirty-two neurons
were tested with CC. Of these, nine were inhibited, nine were facilitated,
and 14 did not respond. Seventeen neurons that responded either to RA or to
CC were tested with stimulation in the pons. Of these, three were
orthodromically activated and two were inhibited from a total of eight
pontine sites. Six of the eight sites were within 300 microns of an area
shown previously to contain neurons that responded to CC. Of 31 additional
sites that were stimulated, but at which stimulation did not drive neurons
that responded to hemodynamic stimuli, 26 were located more than 300
microns from this area (p less than 0.01, X2 test). The data suggest that
some hypothalamic neurons involved in the hemodynamic control of ACTH
release receive a projection from or through the dorsal raphe nucleus
medially, and the ventral locus ceruleus, locus subceruleus, and underlying
reticular formation laterally. However, other neurons may receive
projections that bypass these regions.