2 , 3 Third, in none of our rodent experiments has NT3 treatment caused any detectable hypersensitivity, spasticity, or muscle weakness; rather, after bilateral CST injury in rats, intramuscular delivery of AAV‐preproNT3 reduced spasms, slightly improved grip strength, and showed a trend toward reducing mechanical hyperalgesia. 14 We used fMRI during electrical stimulation of the wrist to explore recovery of somatosensory responsiveness to adhesive patches attached to the wrist.
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Stroke Recovery in Rats after 24-Hour-Delayed Intramuscular Neurotrophin-3 Infusion.
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