Neuroprotective Effect of 6-Paradol in Focal Cerebral Ischemia Involves the Attenuation of Neuroinflammatory Responses in Activated Microglia
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gaire, Bhakta Prasad | - |
dc.contributor.author | Kwon, Oh Wook | - |
dc.contributor.author | Park, Sung Hyuk | - |
dc.contributor.author | Chun, Kwang-Hoon | - |
dc.contributor.author | Kim, Sun Yeou | - |
dc.contributor.author | Shin, Dong Yun | - |
dc.contributor.author | Choi, Ji Woong | - |
dc.date.available | 2020-02-28T09:46:30Z | - |
dc.date.created | 2020-02-06 | - |
dc.date.issued | 2015-03-19 | - |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10696 | - |
dc.description.abstract | Paradols are non-pungent and biotransformed metabolites of shogaols and reduce inflammatory responses as well as oxidative stress as shogaols. Recently, shogaol has been noted to possess therapeutic potential against several central nervous system (CNS) disorders, including cerebral ischemia, by reducing neuroinflammation in microglia. Therefore, paradol could be used to improve neuroinflammation-associated CNS disorders. Here, we synthesized paradol derivatives (2-to 10-paradols). Through the initial screening for antiinflammatory activities using lipopolysaccharide (LPS)-stimulated BV2 microglia, 6-paradol was chosen to be the most effective compound without cytotoxicity. Pretreatment with 6paradol reduced neuroinflammatory responses in LPS-stimulated BV2 microglia by a concentration-dependent manner, which includes reduced NO production by inhibiting iNOS upregulation and lowered secretion of proinflammatory cytokines (IL-6 and TNF-alpha). To pursue whether the beneficial in vitro effects of 6-paradol leads towards in vivo therapeutic effects on transient focal cerebral ischemia characterized by neuroinflammation, we employed middle cerebral artery occlusion (MCAO)/reperfusion (M/R). Administration of 6-paradol immediately after reperfusion significantly reduced brain damage in M/R-challenged mice as assessed by brain infarction, neurological deficit, and neural cell survival and death. Furthermore, as observed in cultured microglia, 6-paradol administration markedly reduced neuroinflammation in M/R-challenged brains by attenuating microglial activation and reducing the number of cells expressing iNOS and TNF-alpha, both of which are known to be produced in microglia following M/R challenge. Collectively, this study provides evidences that 6-paradol effectively protects brain after cerebral ischemia, likely by attenuating neuroinflammation in microglia, suggesting it as a potential therapeutic agent to treat cerebral ischemia. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | PUBLIC LIBRARY SCIENCE | - |
dc.relation.isPartOf | PLOS ONE | - |
dc.subject | TUMOR-NECROSIS-FACTOR | - |
dc.subject | NITRIC-OXIDE SYNTHASE | - |
dc.subject | ZINGIBER-OFFICINALE | - |
dc.subject | CHAIN LENGTH | - |
dc.subject | MICE LACKING | - |
dc.subject | BRAIN-INJURY | - |
dc.subject | FACTOR-ALPHA | - |
dc.subject | GINGER | - |
dc.subject | 6-SHOGAOL | - |
dc.subject | DEFICITS | - |
dc.title | Neuroprotective Effect of 6-Paradol in Focal Cerebral Ischemia Involves the Attenuation of Neuroinflammatory Responses in Activated Microglia | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000351425400140 | - |
dc.identifier.doi | 10.1371/journal.pone.0120203 | - |
dc.identifier.bibliographicCitation | PLOS ONE, v.10, no.3 | - |
dc.identifier.scopusid | 2-s2.0-84925637929 | - |
dc.citation.title | PLOS ONE | - |
dc.citation.volume | 10 | - |
dc.citation.number | 3 | - |
dc.contributor.affiliatedAuthor | Gaire, Bhakta Prasad | - |
dc.contributor.affiliatedAuthor | Kwon, Oh Wook | - |
dc.contributor.affiliatedAuthor | Park, Sung Hyuk | - |
dc.contributor.affiliatedAuthor | Chun, Kwang-Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Sun Yeou | - |
dc.contributor.affiliatedAuthor | Shin, Dong Yun | - |
dc.contributor.affiliatedAuthor | Choi, Ji Woong | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | TUMOR-NECROSIS-FACTOR | - |
dc.subject.keywordPlus | NITRIC-OXIDE SYNTHASE | - |
dc.subject.keywordPlus | ZINGIBER-OFFICINALE | - |
dc.subject.keywordPlus | CHAIN LENGTH | - |
dc.subject.keywordPlus | MICE LACKING | - |
dc.subject.keywordPlus | BRAIN-INJURY | - |
dc.subject.keywordPlus | FACTOR-ALPHA | - |
dc.subject.keywordPlus | GINGER | - |
dc.subject.keywordPlus | 6-SHOGAOL | - |
dc.subject.keywordPlus | DEFICITS | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
1342, Seongnam-daero, Sujeong-gu, Seongnam-si, Gyeonggi-do, Republic of Korea(13120)031-750-5114
COPYRIGHT 2020 Gachon University All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.