Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/68572
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dc.contributor.authorPiyawadee Wichaen_US
dc.contributor.authorJiraporn Tocharusen_US
dc.contributor.authorAdchara Janyouen_US
dc.contributor.authorJinatta Jittiwaten_US
dc.contributor.authorWaraluck Chaichompooen_US
dc.contributor.authorApichart Suksamrarnen_US
dc.contributor.authorChainarong Tocharusen_US
dc.date.accessioned2020-04-02T15:29:47Z-
dc.date.available2020-04-02T15:29:47Z-
dc.date.issued2020-01-01en_US
dc.identifier.issn17341140en_US
dc.identifier.other2-s2.0-85079642570en_US
dc.identifier.other10.1007/s43440-019-00050-9en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85079642570&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/68572-
dc.description.abstract© 2020, Maj Institute of Pharmacology Polish Academy of Sciences. Background: Hexahydrocurcumin (HHC), a major metabolite of curcumin, has been reported to have protective effects against ischemic and reperfusion damage. The goal of the present research was to examine whether HHC could alleviate brain damage and ameliorate functional outcomes by diminishing the blood–brain barrier (BBB) damage that follows cerebral ischemia/reperfusion. Methods: Middle cerebral artery occlusion was induced for 2 h in rats followed by reperfusion. The rats were divided into three groups: sham-operated, vehicle-treated, and HHC-treated groups. At the onset of reperfusion, the rats were immediately intraperitoneally injected with 40 mg/kg HHC. At 48 h after reperfusion, the rats were evaluated for neurological deficits and TTC staining. At 24 h and 48 h after reperfusion, animals were sacrificed, and their brains were extracted. Results: Treatment with HHC reduced neurological scores, infarct volume, morphological changes, Evans blue leakage and immunoglobulin G extravasation. Moreover, HHC treatment reduced BBB damage and neutrophil infiltration, downregulated myeloperoxidase, ICAM-1, and VCAM-1, upregulated tight junction proteins (TJPs), and reduced aquaporin 4 expression and brain water content. Conclusion: These results revealed that HHC treatment preserved the BBB from cerebral ischemia/reperfusion injury by regulating TJPs, attenuating neutrophil infiltration, and reducing brain edema formation. Graphic abstract: [Figure not available: see fulltext.].en_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleHexahydrocurcumin alleviated blood–brain barrier dysfunction in cerebral ischemia/reperfusion ratsen_US
dc.typeJournalen_US
article.title.sourcetitlePharmacological Reportsen_US
article.stream.affiliationsRamkhamhaeng Universityen_US
article.stream.affiliationsMahasarakham Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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