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Combined Effects of Bee Venom Acupuncture and Morphine on Oxaliplatin-Induced Neuropathic Pain in Mice

Authors
Kim, WoojinKim, Min JoonGo, DonghyunMin, Byung-IlNa, Heung SikKim, Sun Kwang
Issue Date
Feb-2016
Publisher
MDPI
Keywords
bee venom acupuncture; chemotherapy induced neuropathic pain; morphine; oxaliplatin
Citation
TOXINS, v.8, no.2
Indexed
SCIE
SCOPUS
Journal Title
TOXINS
Volume
8
Number
2
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/89665
DOI
10.3390/toxins8020033
ISSN
2072-6651
Abstract
Oxaliplatin, a chemotherapeutic drug for colorectal cancer, induces severe peripheral neuropathy. Bee venom acupuncture (BVA) has been used to attenuate pain, and its effect is known to be mediated by spinal noradrenergic and serotonergic receptors. Morphine is a well-known opioid used to treat different types of pain. Here, we investigated whether treatment with a combination of these two agents has an additive effect on oxaliplatin-induced neuropathic pain in mice. To assess cold and mechanical allodynia, acetone and von Frey filament tests were used, respectively. Significant allodynia signs were observed three days after an oxaliplatin injection (6 mg/kg, i.p.). BVA (0.25, 1, and 2.5 mg/kg, s.c., ST36) or morphine (0.5, 2, and 5 mg/kg, i.p.) alone showed dose-dependent anti-allodynic effects. The combination of BVA and morphine at intermediate doses showed a greater and longer effect than either BVA or morphine alone at the highest dose. Intrathecal pretreatment with the opioidergic (naloxone, 20 g) or 5-HT3 (MDL-72222, 15 g) receptor antagonist, but not with (2)-adrenergic (idazoxan, 10 g) receptor antagonist, blocked this additive effect. Therefore, we suggest that the combination effect of BVA and morphine is mediated by spinal opioidergic and 5-HT3 receptors and this combination has a robust and enduring analgesic action against oxaliplatin-induced neuropathic pain.
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