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Primary afferent terminal sprouting after a cervical dorsal rootlet section in the macaque monkey
1Department of Comparative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA. cdarian@stanford.edu
The Journal of Comparative Neurology
|January 30, 2004
Summary
Primary afferent neurons sprout after cervical dorsal root injury, leading to somatosensory cortex reactivation. This study shows spared neurons in the dorsal horn and cuneate nucleus contribute to functional recovery.
Area of Science:
- Neuroscience
- Somatosensory System
- Neural Plasticity
Background:
- Localized cervical dorsal root lesions can cause temporary silencing of cortical representations.
- Subsequent re-emergence of these representations suggests underlying neural plasticity mechanisms.
Purpose of the Study:
- To investigate if central axonal sprouting of primary afferent neurons mediates somatosensory cortical reactivation after a dorsal root lesion.
- To provide direct evidence for sprouting in specific spinal cord regions.
Main Methods:
- Electrophysiological mapping of hand representation in the macaque somatosensory cortex.
- Injection of cholera toxin subunit B-horseradish peroxidase into digit pads to label primary afferent central terminals.
- Assessment of primary afferent terminal proliferation in the spinal dorsal horn and cuneate nucleus at different postlesion time points.
Main Results:
- Cortical representations of digits C6-C8 initially silenced after dorsal rootlet section, then re-emerged over 2-4 months.
- Physiologically detectable input from lesioned digits emerged in bordering dorsal rootlets.
- Significantly larger labeled terminal bouton distributions were observed in the dorsal horn and cuneate nucleus on the lesion side at 15-25 weeks compared to 7 days postlesion.
Conclusions:
- Sprouting of spared primary afferent terminals in the dorsal horn and cuneate nucleus occurs after restricted dorsal root injury.
- This axonal sprouting is a key mechanism underlying the observed somatosensory cortical reactivation.