期刊论文详细信息
Journal of Pharmacological Sciences
Establishment of Opioid-Induced Rewarding Effects Under Oxaliplatin- and Paclitaxel-Induced Neuropathy in Rats
Tomohisa Mori1  Aki Masumoto1  Atsushi Nakamura1  Gaku Sakaguchi2  Sachiko Komiya1  Tomoe Kanbara1  Toshiyuki Kanemasa2  Yoshiyuki Iwase1  Masato Harumiya1  Masahiro Shibasaki1  Tsutomu Suzuki1 
[1] Department of Toxicology, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Japan;Pain & Neurology, Discovery Research Laboratories, Shionogi & Co., Ltd., Japan
关键词: rewarding effect;    oxaliplatin;    paclitaxel;    neuropathic pain;    μ-opioid receptor agonist;   
DOI  :  10.1254/jphs.14134FP
学科分类:药学
来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society
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【 摘 要 】

References(30)Cited-By(3)The rewarding effects of μ-receptor agonists can be suppressed under several pain conditions. We recently showed that clinically used μ-receptor agonists possess efficacies for relieving the neuropathic pain induced by chemotherapeutic drug in rats; however, it is possible that the use of μ-receptor agonists may trigger the rewarding effects even under chemotherapeutic drug–induced neuropathic pain. Nevertheless, no information is available regarding whether μ-receptor agonists produce psychological dependence under chemotherapeutic drug–induced neuropathic pain. Therefore, we examined the effects of neuropathy induced by chemotherapeutic drugs on the rewarding effects of morphine, oxycodone, and fentanyl in rats. Repeated treatment with oxaliplatin or paclitaxel produced neuropathy as measured by the von Frey test. Rewarding effects produced by antinociceptive doses of μ-receptor agonists were not suppressed under oxaliplatin- or paclitaxel-induced neuropathy. Furthermore, the morphine-induced increase in the release of dopamine from the nucleus accumbens, which is a critical step in the rewarding effects of μ-receptor agonists, was not altered in paclitaxel-treated rats. These results suggest that the rewarding effects of μ-receptor agonists can still be established under oxaliplatin- or paclitaxel-induced neuropathic pain. Therefore, patients should be carefully monitored for psychological dependence on μ-receptor agonists when they are used to control chemotherapeutic drug-induced neuropathic pain.

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