Antinociceptive Effects of the Serotonin and Noradrenaline Reuptake Inhibitors Milnacipran and Duloxetine on Vincristine-Induced Neuropathic Pain Model in MiceReport as inadecuate




Antinociceptive Effects of the Serotonin and Noradrenaline Reuptake Inhibitors Milnacipran and Duloxetine on Vincristine-Induced Neuropathic Pain Model in Mice - Download this document for free, or read online. Document in PDF available to download.

ISRN Pain - Volume 2014 2014, Article ID 915464, 7 pages -

Research Article

Department of Clinical Pharmaceutics, Tohoku Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai 981-8558, Japan

Department of Pharmacology, Daiichi College of Pharmaceutical Sciences, 22-1 Tamagawa-cho, Minami-ku, Fukuoka 815-8511, Japan

Received 24 December 2013; Accepted 14 January 2014; Published 23 February 2014

Academic Editors: D. Balayssac, C. Courteix, J. Ferreira, M. Takeda, and M. Tsuruoka

Copyright © 2014 Soh Katsuyama et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Vincristine is an anticancer drug used to treat a variety of cancer types, but it frequently causes peripheral neuropathy. Neuropathic pain is often associated with the appearance of abnormal sensory signs, such as allodynia. Milnacipran and duloxetine, serotonin-noradrenaline reuptake inhibitors, have shown efficacy against several chronic pain syndromes. In this study, we investigated the attenuation of vincristine-induced mechanical allodynia in mice by milnacipran and duloxetine. To induce peripheral neuropathy, vincristine was administered once per day 0.1 mg-kg, intraperitoneally i.p. for 7 days. Mechanical allodynia was evaluated by measuring the withdrawal response to stimulation with a von Frey filament. In vincristine-treated mice, mechanical allodynia was observed on days 3–28 of vincristine administration. A single administration of milnacipran 40 mg-kg, i.p. or duloxetine 20 mg-kg, i.p. had no effect on vincristine-induced mechanical allodynia. However, repeated administration of milnacipran 20 or 40 mg-kg, once per day, i.p. or duloxetine 5, 10, or 20 mg-kg, once per day, i.p. for 7 days significantly reduced vincristine-induced mechanical allodynia. These results suggest that chronic vincristine administration induces mechanical allodynia, and that repeated milnacipran and duloxetine administration may be an effective approach for the treatment of neuropathic pain caused by vincristine treatment for cancer.





Author: Soh Katsuyama, Hiromu Aso, Akira Otowa, Tomomi Yagi, Yukinaga Kishikawa, Takaaki Komatsu, Tsukasa Sakurada, and Hitoshi Nak

Source: https://www.hindawi.com/



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