Abstract
The role of dopamine (DA) on motor cortical pyramidal tract neurons (PTNs) was studied in anesthetized cats with in vivo extracellular recordings in response to transcallosal (TC) and ventrolateral (VL) thalamic stimulations. An antidromic PT potential was evoked to recognize PTNs. In most PTNs, iontophoretic application of DA significantly reduced the spike activity exerted by 20 single-pulse stimulations. Both D(1)-like and D(2)-like receptor antagonists blocked (disinhibited) the effect in a similar way regardless of TC and VL stimulations, suggesting colocalization of two receptors. Except for the presence of jittering, the mean latency was usually fixed and short. These findings indicate that ventral midbrain DA imposes an intense suppression in modulating PTNs response to both callosal and thalamocortical excitatory inputs in motor cortex. Such DAergic suppression could play pivotal role to improve motor and sensorimotor signal integration.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Action Potentials / drug effects
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Action Potentials / physiology
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Animals
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Cats
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Corpus Callosum / cytology
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Corpus Callosum / drug effects
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Corpus Callosum / metabolism
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Dopamine / metabolism*
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Dopamine / pharmacology
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Excitatory Postsynaptic Potentials / drug effects
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Excitatory Postsynaptic Potentials / physiology
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Motor Cortex / cytology
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Motor Cortex / drug effects
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Motor Cortex / metabolism*
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Neural Inhibition / drug effects
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Neural Inhibition / physiology*
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Neural Pathways / cytology
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Neural Pathways / drug effects
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Neural Pathways / metabolism
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Neurons / cytology
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Neurons / drug effects
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Neurons / metabolism*
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Pyramidal Tracts / cytology
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Pyramidal Tracts / drug effects
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Pyramidal Tracts / metabolism*
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Synapses / drug effects
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Synapses / metabolism*
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Ventral Tegmental Area / cytology
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Ventral Tegmental Area / drug effects
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Ventral Tegmental Area / metabolism
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Ventral Thalamic Nuclei / cytology
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Ventral Thalamic Nuclei / drug effects
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Ventral Thalamic Nuclei / metabolism