Additive antinociceptive effects of a combination of vitamin C and vitamin E after peripheral nerve injury.

PLoS One

pharmazentrum frankfurt/ZAFES, Institut für Klinische Pharmakologie, Klinikum der Goethe-Universität, Frankfurt am Main, Germany.

Published: August 2012

AI Article Synopsis

  • Increasing reactive oxygen species (ROS) levels are linked to enhanced pain sensitivity, particularly in persistent pain conditions.
  • A study found that a combination of vitamins C and E reduced pain responses in mouse models of inflammatory and neuropathic pain, while the individual vitamins did not show similar effects.
  • The combination therapy decreased specific cellular changes in the spinal cord and improved pain symptoms when ROS were introduced, indicating their potential for pain relief through antioxidant action.

Article Abstract

Accumulating evidence indicates that increased generation of reactive oxygen species (ROS) contributes to the development of exaggerated pain hypersensitivity during persistent pain. In the present study, we investigated the antinociceptive efficacy of the antioxidants vitamin C and vitamin E in mouse models of inflammatory and neuropathic pain. We show that systemic administration of a combination of vitamins C and E inhibited the early behavioral responses to formalin injection and the neuropathic pain behavior after peripheral nerve injury, but not the inflammatory pain behavior induced by Complete Freund's Adjuvant. In contrast, vitamin C or vitamin E given alone failed to affect the nociceptive behavior in all tested models. The attenuated neuropathic pain behavior induced by the vitamin C and E combination was paralleled by a reduced p38 phosphorylation in the spinal cord and in dorsal root ganglia, and was also observed after intrathecal injection of the vitamins. Moreover, the vitamin C and E combination ameliorated the allodynia induced by an intrathecally delivered ROS donor. Our results suggest that administration of vitamins C and E in combination may exert synergistic antinociceptive effects, and further indicate that ROS essentially contribute to nociceptive processing in special pain states.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237606PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0029240PLOS

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