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High-dose dextromethorphan produces myelinoid bodies in the hippocampus of rats

Authors
Hai-Quyen TranChung, Yoon HeeShin, Eun-JooKim, Won KiLee, Jae-ChulJeong, Ji HoonWie, Myung BokJang, Choon-GonYamada, KiyofumiNabeshima, ToshitakaKim, Hyoung-Chun
Issue Date
10월-2016
Publisher
JAPANESE PHARMACOLOGICAL SOC
Keywords
High-dose dextromethorphan; Administration route; Myelinoid bodies with mitochondrial dysfunction
Citation
JOURNAL OF PHARMACOLOGICAL SCIENCES, v.132, no.2, pp.166 - 170
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PHARMACOLOGICAL SCIENCES
Volume
132
Number
2
Start Page
166
End Page
170
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/87234
DOI
10.1016/j.jphs.2016.10.001
ISSN
1347-8613
Abstract
Dextromethorphan (DM) administered at supra-antitussive doses produce psychotoxic and neurotoxic effects in humans. We administered DM (80 mg/kg) to rats intraperitoneally to determine the ultrastructural change induced by DM, because intraperitoneal route is sensitive for the behavioral responses. Treatment with DM resulted in mitochondrial dysfunction and formation of myelinoid bodies in the hippocampus. MK-801 [(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine maleate] attenuated DM-induced cytosolic oxidative burdens. However, neither MK-801 nor naloxone affected DM-induced mitochondrial dysfunction and formation of myelinoid bodies, indicating that the neurotoxic mechanism needs to be further elucidated. Therefore, the spectrum of toxicological effects associated with DM need to be reassessed. (C) 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
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