Cited 5 times in
Adjudin prevents neuronal damage and neuroinflammation via inhibiting mTOR activation against pilocarpine-induced status epilepticus
DC Field | Value | Language |
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dc.contributor.author | 김원주 | - |
dc.date.accessioned | 2022-07-08T03:12:03Z | - |
dc.date.available | 2022-07-08T03:12:03Z | - |
dc.date.issued | 2022-05 | - |
dc.identifier.issn | 0361-9230 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/188719 | - |
dc.description.abstract | Inflammatory responses in the brain play an etiological role in the development of epilepsy, suggesting that finding novel molecules for controlling neuroinflammation may have clinical value in developing the disease-modifying strategies for epileptogenesis. Adjudin, a multi-functional small molecule compound, has pleiotropic effects, including anti-inflammatory properties. In the present study, we aimed to investigate the effects of adjudin on pilocarpine-induced status epilepticus (SE) and its role in the regulation of reactive gliosis and neuroinflammation. SE was induced in male C57BL/6 mice that were then treated with adjudin (50 mg/kg) for 3 days after SE onset. Immunofluorescence staining, terminal deoxynucleotidyl transferase dUTP nick end labeling staining, and western blot analysis were used to evaluate the effects of adjudin treatment in the hippocampus after SE. Our results showed that adjudin treatment significantly mitigated apoptotic cell death in the hippocampus after SE onset. Moreover, adjudin treatment suppressed SE-induced glial activation and activation of mammalian target of rapamycin signaling in the hippocampus. Concomitantly, adjudin treatment significantly reduced SE-induced inflammatory processes, as confirmed by changes in the expression of inflammatory mediators such as tumor necrosis factor-α, interleukin-1β, and arginase-1. In conclusion, these findings suggest that adjudin may serve as a potential neuroprotective agent for preventing pathological mechanisms implicated in epileptogenesis | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier Science | - |
dc.relation.isPartOf | BRAIN RESEARCH BULLETIN | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Hydrazines | - |
dc.subject.MESH | Indazoles | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mammals | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Mice, Inbred C57BL | - |
dc.subject.MESH | Neuroinflammatory Diseases | - |
dc.subject.MESH | Pilocarpine* / toxicity | - |
dc.subject.MESH | Status Epilepticus* / chemically induced | - |
dc.subject.MESH | Status Epilepticus* / drug therapy | - |
dc.subject.MESH | TOR Serine-Threonine Kinases | - |
dc.title | Adjudin prevents neuronal damage and neuroinflammation via inhibiting mTOR activation against pilocarpine-induced status epilepticus | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Neurology (신경과학교실) | - |
dc.contributor.googleauthor | Soojin Park | - |
dc.contributor.googleauthor | Jing Zhu | - |
dc.contributor.googleauthor | Kyoung Hoon Jeong | - |
dc.contributor.googleauthor | Won-Joo Kim | - |
dc.identifier.doi | 10.1016/j.brainresbull.2022.02.009 | - |
dc.contributor.localId | A00771 | - |
dc.relation.journalcode | J00393 | - |
dc.identifier.eissn | 1873-2747 | - |
dc.identifier.pmid | 35182690 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S036192302200048X?via%3Dihub | - |
dc.subject.keyword | Adjudin | - |
dc.subject.keyword | Anti-inflammatory effects | - |
dc.subject.keyword | Hippocampus | - |
dc.subject.keyword | Neuroprotection | - |
dc.subject.keyword | Status epilepticus | - |
dc.contributor.alternativeName | Kim, Won Joo | - |
dc.contributor.affiliatedAuthor | 김원주 | - |
dc.citation.volume | 182 | - |
dc.citation.startPage | 80 | - |
dc.citation.endPage | 89 | - |
dc.identifier.bibliographicCitation | BRAIN RESEARCH BULLETIN, Vol.182 : 80-89, 2022-05 | - |
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