Prophylactic administration of aucubin inhibits paclitaxel-induced mechanical allodynia via the inhibition of endoplasmic reticulum stress in peripheral Schwann cells

Tsugunobu Andoh*, Daisuke Uta, Mitsuru Kato, Kazufumi Toume, Katsuko Komatsu, Yasushi Kuraishi

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Paclitaxel is a chemotherapeutic agent that causes peripheral neuropathy as its major dose-limiting side effect. However, the peripheral neuropathy is difficult to manage. A study we recently conducted showed that repetitive administration of aucubin as a prophylactic inhibits paclitaxel-induced mechanical allodynia. However, the mechanisms underlying the anti-allodynic activity of aucubin, which is a major component of Plantaginis Semen, was unclear. In addition to mechanical allodynia, aucubin inhibited spontaneous and mechanical stimuli-induced firing in spinal dorsal horn neurons; however, catalpol, a metabolite of aucubin, did not show these effects. Furthermore, paclitaxel induced the expression of CCAAT/enhancer-binding protein homologous protein, a marker of endoplasmic reticulum (ER) stress, in the sciatic nerve and a Schwann cell line (LY-PPB6 cells); however, this effect was inhibited by aucubin. These results suggest that aucubin inhibits paclitaxel-induced mechanical allodynia through the inhibition of ER stress in peripheral Schwann cells.

Original languageEnglish
Pages (from-to)473-478
Number of pages6
JournalBiological and Pharmaceutical Bulletin
Volume40
Issue number4
DOIs
StatePublished - 2017

Keywords

  • Aucubin
  • Firing
  • Mechanical allodynia
  • Paclitaxel
  • Schwann cell
  • Stress

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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