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Vol. 303, Issue 2, 497-502, November 2002
Laboratory of Cerebral Metabolism, National Institute of Mental
Health (T.E., Y.I., M.C., J.J., L.S.), and The Positron Emission
Tomography Department, Clinical Center (K.S.), National Institutes of
Health, Bethesda, Maryland
Local cerebral blood flow (CBF) was determined in 30 cerebral
structures, including four structures of the whisker-to-barrel cortex
sensory pathway, by the quantitative autoradiographic
[14C]iodoantipyrine method during unilateral vibrissal
stimulation in rats administered 0.1 or 1.0 mg/kg haloperidol or its
control vehicle intravenously. The low dose of haloperidol had no
significant effects on resting CBF or its enhancement by vibrissal
stimulation. By standard t tests, the high dose
statistically significantly lowered baseline CBF in frontal and visual
cortex, hippocampus, dentate gyrus, inferior olive, cerebellar cortex,
and the ventral posteromedial (VPM) thalamic nucleus on the
unstimulated side, and raised baseline CBF in the lateral habenula;
however, these changes lost statistical significance after Bonferroni
correction for multiple comparisons. Neither dose had any effects on
the increases in CBF evoked by vibrissal stimulation in the principal sensory trigeminal nucleus and barrel cortex, but the higher dose statistically significantly enhanced the percent increases in CBF due
to the sensory stimulation in the spinal trigeminal nucleus and VPM
thalamic nucleus. These results do not support a role for direct
dopaminergic vasoactive mechanisms in the increases in CBF associated
with neuronal functional activation.
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