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Phrenic nerve inputs to upper cervical (C1-C3) spinothalamic tract neurons in monkeys
M J Chandler1, J Zhang, R D Foreman
1Department of Physiology, University of Oklahoma Health Sciences Center, P.O. Box 26901, Oklahoma City, OK 73190, USA. margaret-chandler@ouhsc.edu
Brain Research
|July 17, 1998
Summary
High cervical spinothalamic (STT) neurons in monkeys are primarily activated by thoracic phrenic nerve input. Diaphragmatic input has a lesser effect, suggesting a role in processing pain signals.
Area of Science:
- Neuroscience
- Spinal Cord Physiology
- Pain Pathways
Background:
- Spinothalamic tract (STT) neurons in the upper cervical spinal cord process sensory information.
- Previous studies in monkeys indicated mid-cervical STT neurons respond to phrenic afferent input from the diaphragm.
- Rodent studies show differential phrenic nerve input organization in dorsal horn neurons.
Purpose of the Study:
- To investigate if high cervical STT neurons in primates are preferentially activated by phrenic inputs from thoracic structures.
- To compare responses to ipsilateral phrenic nerve stimulation above and below the heart.
- To assess the influence of contralateral phrenic input on these neurons.
Main Methods:
- Extracellular recordings of C1-C3 STT neuron discharge rates in monkeys.
- Electrical stimulation of ipsilateral and contralateral phrenic nerve fibers.
- Comparison of responses to stimulation from phrenic input originating above and below the heart.
Main Results:
- Upper cervical STT neurons showed strongest excitation from ipsilateral, small-diameter phrenic fibers originating in thoracic structures.
- Group III and IV input from diaphragmatic phrenic fibers had a lesser excitatory effect.
- Contralateral phrenic input also demonstrated a reduced effect on C1-C3 STT neurons.
Conclusions:
- High cervical STT neurons in monkeys are preferentially responsive to phrenic input from thoracic structures.
- Differential organization of phrenic afferent input suggests a role in sensory processing, potentially including nociception.
- Lesser activation by diaphragmatic and contralateral inputs may indicate their involvement in pain signaling pathways.