ArticleExperimental brain research2019
Quantitative assessment of cortical somatosensory digit representations after median and ulnar nerve injury in rats.
Article in Experimental brain research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed, 7 citations in OpenAlex.
- Vagus nerve stimulation does not improve recovery of forelimb motor or somatosensory function in a model of neuropathic pain.Scientific reports · 2022Article
- The tactile experience paired with vagus nerve stimulation determines the degree of sensory recovery after chronic nerve damage.Behavioural brain research · 2021Article
- Investigating the effects of transcranial alternating current stimulation on primary somatosensory cortex.Scientific reports · 2020Article
- Radial nerve injury causes long-lasting forelimb sensory impairment and motor dysfunction in rats.Pain reportsArticle
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Authors and funding
4 authors at 2 institutions in 1 country.
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Abstract
Incomplete recovery of sensory function is common after peripheral nerve injury (PNI). Despite reinnervation following injury, disorganized cortical representations persist and may contribute to functional deficits. There is a dearth of literature characterizing cortical responses after PNI in rodent models. Here we develop a quantitative electrophysiological method for mapping forepaw digit responses in primary somatosensory cortex (S1) of rats. We tested the hypothesis that PNI in the forelimb would generate significant, long lasting sensory deficits, and corresponding disorganization in S1. Rats underwent a transection of the proximal segment of the median and ulnar nerves in the forelimb followed by tubular repair. 4-12 months after nerve injury, we tested mechanosensory withdrawal thresholds and mapped S1 responses to mechanical stimulation of the digits. PNI produces persistent elevation of mechanical withdrawal thresholds, consistent with an impairment in sensory function. Assessment of cortical neurophysiology reveals a substantial disorganization of S1 somatotopy. Additionally, we document degraded timing and digit specificity of cortical responses. This quantitative measurement of long-term changes in S1 digit representations after forelimb nerve injury in rodents provides a framework for further studies focused on the development of therapeutic strategies to restore cortical and sensory function.
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