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*Department of Anesthesiology, Osaka Medical College, Takatsuki, Japan;
Research and Development, Maruishi Pharmaceutical Co. Ltd., Osaka, Japan; and
Department of Medical Chemistry, Kansai Medical University, Moriguchi, Japan
Address correspondence and reprint requests to Seiji Ito, MD, PhD, Department of Medical Chemistry, Kansai Medical University, 10-15 Fumizono, Moriguchi 570-8506, Japan. Address e-mail to ito{at}takii.kmu.ac.jp
Although intradermal injection of capsaicin produces acute pain and secondary hyperalgesia, long-term topical application of capsaicin cream has been used as a medication for pain relief in various pain conditions. We previously reported that intrathecal administration of prostaglandin (PG) E2 and PGF2
into mice induced touch-evoked pain (allodynia) through capsaicin-sensitive and capsaicin-insensitive afferent fibers, respectively. To clarify the mechanism of an analgesic effect by capsaicin cream, here we applied it to the tail and hind paws of mice and investigated its effects on PGE2- and PGF2
-induced allodynia. Twenty-four-hour pretreatment of mice with 0.025% or 0.05% capsaicin cream markedly alleviated allodynia induced by PGE2, but not by PGF2
. These results suggest that the topical application of capsaicin cream modulates capsaicin-sensitive afferents and ameliorates allodynia evoked by PGE2 at the spinal level.
IMPLICATIONS: Topical application of capsaicin cream alleviates touch-evoked pain induced by the intrathecal administration of prostaglandin E2. This study may provide a rationale for the use of capsaicin cream as a therapeutic drug for pain relief.
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