scispace - formally typeset
K

Kendall Mitchell

Researcher at National Institutes of Health

Publications -  9
Citations -  306

Kendall Mitchell is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Nociception & Resiniferatoxin. The author has an hindex of 7, co-authored 9 publications receiving 275 citations.

Papers
More filters
Journal ArticleDOI

Ablation of rat TRPV1-expressing Adelta/C-fibers with resiniferatoxin: analysis of withdrawal behaviors, recovery of function and molecular correlates

TL;DR: Behavioral recovery following peripheral RTX treatment is linked to regeneration of TRPV1-expressing Adelta and C-fibers and sustained expression of molecular markers and Infrared laser stimulation is a potentially valuable tool for evaluating the behavioral role of Adelta fibers in pain and pain control.
Journal ArticleDOI

Prolonged analgesic response of cornea to topical resiniferatoxin, a potent TRPV1 agonist

TL;DR: Topical RTX analgesia did not impair epithelial wound healing, left the blink reflex intact and occurred without detectable histological damage to the cornea, suggesting that RTX may be a safe and effective treatment for post‐operative or post‐injury ophthalmic pain.
Journal ArticleDOI

Nociception and inflammatory hyperalgesia evaluated in rodents using infrared laser stimulation after Trpv1 gene knockout or resiniferatoxin lesion

TL;DR: It is shown that stimulating either subtype of TRPV1+ fiber in the paw during carrageenan‐induced inflammation or following hind‐paw incision elicits pronounced hyperalgesic responses, including prolonged paw guarding, which suggest multiple roles for TRPv1+ A&dgr; fibers in nociceptive processes and their modulation of pathological pain conditions.
Journal ArticleDOI

Peripheral inflammation increases Scya2 expression in sensory ganglia and cytokine and endothelial related gene expression in inflamed tissue

TL;DR: The results are consistent with the idea that monocyte chemoattractant protein‐1 at the site of peripheral injury and/or in DRG is involved in inflammatory hyperalgesia.
Journal ArticleDOI

Localization of S100A8 and S100A9 expressing neutrophils to spinal cord during peripheral tissue inflammation.

TL;DR: The data raise the possibility that selective populations of leukocytes may communicate the presence of disease or tissue damage from the periphery to cells in the central nervous system through the endothelial blood–brain barrier.