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Effect of zolpidem on functional recovery in a rat model of ischemic stroke

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dc.contributor.authorOh, Min-Kyun-
dc.contributor.authorYoon, Kyung Jae-
dc.contributor.authorLee, Yong-Taek-
dc.contributor.authorChae, Seoung Wan-
dc.contributor.authorChoi, Hye Young-
dc.contributor.authorShin, Hee Suk-
dc.contributor.authorPark, Yun Hee-
dc.contributor.authorChun, Se-Woong-
dc.contributor.authorPark, Young Sook-
dc.date.accessioned2022-12-26T17:17:57Z-
dc.date.available2022-12-26T17:17:57Z-
dc.date.issued2018-01-
dc.identifier.issn0300-0605-
dc.identifier.issn1473-2300-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/12009-
dc.description.abstractObjective To evaluate the effects of zolpidem on functional recovery in a rat model of acute ischemic stroke. Methods Following ischemic stroke procedures, 42 rats (six in each group) were randomly assigned to receive zolpidem (0.1, 0.25, 0.5, 1.0, 2.0 or 4.0mg/kg) or normal saline administer intraperitoneally once daily for two weeks. Motor behavioural index (MBI) scores, radial 8-arm maze (RAM) test times and brain MRI scans were obtained 24 hours (Day 1) and two weeks (Day 14) post-procedure. Immunohistochemistry was performed on Day 14. Results By comparison with the normal saline group, the 0.5 and 1.0mg/kg zolpidem groups showed statistically significant improvements in MBI scores and increased numbers of brain-derived neurotrophic factor (BDNF) stained cells over the two week dosing period. By contrast, the 4.0mg/kg zolpidem group had statistically significantly impaired MBI scores compared with the control group. No differences among groups were found in RAM times or infarction volumes. Conclusions This study in a rat model showed that 0.5-1.0mg/kg of zolpidem had beneficial effects on behavioural recovery by enhancing neural plasticity without causing any memory impairment in acute ischemic stroke.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherSAGE PUBLICATIONS LTD-
dc.titleEffect of zolpidem on functional recovery in a rat model of ischemic stroke-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1177/0300060517723799-
dc.identifier.scopusid2-s2.0-85041377997-
dc.identifier.wosid000419863700027-
dc.identifier.bibliographicCitationJOURNAL OF INTERNATIONAL MEDICAL RESEARCH, v.46, no.1, pp 249 - 257-
dc.citation.titleJOURNAL OF INTERNATIONAL MEDICAL RESEARCH-
dc.citation.volume46-
dc.citation.number1-
dc.citation.startPage249-
dc.citation.endPage257-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusCEREBRAL-ARTERY OCCLUSION-
dc.subject.keywordPlusCORTICAL PLASTICITY-
dc.subject.keywordPlusINSOMNIA-
dc.subject.keywordPlusMEMORY-
dc.subject.keywordPlusTRIAZOLAM-
dc.subject.keywordPlusANTIOXIDANT-
dc.subject.keywordPlusDAMAGE-
dc.subject.keywordAuthorZolpidem-
dc.subject.keywordAuthorinsomnia-
dc.subject.keywordAuthorstroke-
dc.subject.keywordAuthorrecovery-
dc.subject.keywordAuthorischemia-
dc.subject.keywordAuthorrat model of ischemic stroke-
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