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

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dc.contributor.authorKim, Woojin-
dc.contributor.authorKim, Min Joon-
dc.contributor.authorGo, Donghyun-
dc.contributor.authorMin, Byung-Il-
dc.contributor.authorNa, Heung Sik-
dc.contributor.authorKim, Sun Kwang-
dc.date.accessioned2021-09-04T03:29:14Z-
dc.date.available2021-09-04T03:29:14Z-
dc.date.created2021-06-18-
dc.date.issued2016-02-
dc.identifier.issn2072-6651-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/89665-
dc.description.abstractOxaliplatin, 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.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI-
dc.subjectINDUCED PERIPHERAL NEUROPATHY-
dc.subjectACUPOINT STIMULATION-
dc.subjectFORMALIN TEST-
dc.subjectOPIOID RESPONSIVENESS-
dc.subjectRAT MODEL-
dc.subjectAPIPUNCTURE-
dc.subjectMANAGEMENT-
dc.subjectBEHAVIOR-
dc.subjectANTINOCICEPTION-
dc.subjectINVOLVEMENT-
dc.titleCombined Effects of Bee Venom Acupuncture and Morphine on Oxaliplatin-Induced Neuropathic Pain in Mice-
dc.typeArticle-
dc.contributor.affiliatedAuthorNa, Heung Sik-
dc.identifier.doi10.3390/toxins8020033-
dc.identifier.scopusid2-s2.0-84957556326-
dc.identifier.wosid000371831200012-
dc.identifier.bibliographicCitationTOXINS, v.8, no.2-
dc.relation.isPartOfTOXINS-
dc.citation.titleTOXINS-
dc.citation.volume8-
dc.citation.number2-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusINDUCED PERIPHERAL NEUROPATHY-
dc.subject.keywordPlusACUPOINT STIMULATION-
dc.subject.keywordPlusFORMALIN TEST-
dc.subject.keywordPlusOPIOID RESPONSIVENESS-
dc.subject.keywordPlusRAT MODEL-
dc.subject.keywordPlusAPIPUNCTURE-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusANTINOCICEPTION-
dc.subject.keywordPlusINVOLVEMENT-
dc.subject.keywordAuthorbee venom acupuncture-
dc.subject.keywordAuthorchemotherapy induced neuropathic pain-
dc.subject.keywordAuthormorphine-
dc.subject.keywordAuthoroxaliplatin-
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