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Neurons in the hippocampal CA1 region, but not the dentate gyrus, are susceptible to oxidative stress in rats with streptozotocin-induced type 1 diabetes

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dc.contributor.authorLee, Sang Gun-
dc.contributor.authorYoo, Dae Young-
dc.contributor.authorJung, Hyo Young-
dc.contributor.authorNam, Sung Min-
dc.contributor.authorKim, Jong Whi-
dc.contributor.authorChoi, Jung Hoon-
dc.contributor.authorYi, Sun Shin-
dc.contributor.authorWon, Moo-Ho-
dc.contributor.authorYoon, Yeo Sung-
dc.contributor.authorHwang, In Koo-
dc.contributor.authorMoon, Seung Myung-
dc.date.accessioned2021-08-11T20:44:12Z-
dc.date.available2021-08-11T20:44:12Z-
dc.date.issued2015-03-
dc.identifier.issn1673-5374-
dc.identifier.issn1876-7958-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/10849-
dc.description.abstractIn this study, we investigated the effects of streptozotocin-induced type 1 diabetes on antioxidant-like protein-1 immunoreactivity, protein carbonyl levels, and malondialdehyde formation, a marker for lipid peroxidation, in the hippocampus. For this study, streptozotocin (75 mg/kg) was intraperitoneally injected into adult rats to induce type 1 diabetes. The three experimental parameters were determined at 2, 3, 4 weeks after streptozotocin treatment. Fasting blood glucose levels significantly increased by 20.7-21.9 mM after streptozotocin treatment. The number of antioxidant-like protein-1 immunoreactive neurons significantly decreased in the hippocampal CA1 region, but not the dentate gyrus, 3 weeks after streptozotocin treatment compared to the control group. Malondialdehyde and protein carbonyl levels, which are modified by oxidative stress, significantly increased with a peak at 3 weeks after malondialdehyde treatment, and then decreased 4 weeks after malondialdehyde treatment. These results suggest that neurons in the hippocampal CA1 region, but not the dentate gyrus, are susceptible to oxidative stress 3 weeks after malondialdehyde treatment.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherNeural Regeneration Research-
dc.titleNeurons in the hippocampal CA1 region, but not the dentate gyrus, are susceptible to oxidative stress in rats with streptozotocin-induced type 1 diabetes-
dc.typeArticle-
dc.publisher.location인도-
dc.identifier.doi10.4103/1673-5374.153695-
dc.identifier.scopusid2-s2.0-84926207555-
dc.identifier.wosid000353740000027-
dc.identifier.bibliographicCitationNeural Regeneration Research, v.10, no.3, pp 451 - 456-
dc.citation.titleNeural Regeneration Research-
dc.citation.volume10-
dc.citation.number3-
dc.citation.startPage451-
dc.citation.endPage456-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusANTIOXIDANT PROTEIN-
dc.subject.keywordPlusFREE-RADICALS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusMELLITUS-
dc.subject.keywordPlusREDUCTASE-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthornerve regeneration-
dc.subject.keywordAuthorhippocampus-
dc.subject.keywordAuthordentate gyrus-
dc.subject.keywordAuthorlipid peroxidation-
dc.subject.keywordAuthortype 1 diabetes-
dc.subject.keywordAuthormalondialdehyde-
dc.subject.keywordAuthorneurons-
dc.subject.keywordAuthorneural regeneration-
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