Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13442
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dc.contributor.authorKeowkase R.
dc.contributor.authorWeerapreeyakul N.
dc.date.accessioned2021-04-05T03:23:58Z-
dc.date.available2021-04-05T03:23:58Z-
dc.date.issued2016
dc.identifier.issn320943
dc.identifier.other2-s2.0-84957705999
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13442-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84957705999&doi=10.1055%2fs-0041-111621&partnerID=40&md5=f95aef1b53bfd998cad65a62d7349375
dc.description.abstractAmyloid-β, one of the hallmarks of Alzheimer's disease, is toxic to neurons and causes cell death in the brain. Oxidative stress is known to play an important role in Alzheimer's disease, and there is strong evidence linking oxidative stress to amyloid-β. The herbal plant Tiew kon (Cratoxylum formosum ssp. pruniflorum) is an indigenous vegetable that is grown in Southeast Asia. Many reports suggested that the twig extract from C. formosum possesses an antioxidant property. The purpose of this study was to investigate the protective effect of the twig extract from C. formosum against amyloid-β toxicity using the transgenic Caenorhabditis elegans model. This study demonstrated that the extract significantly delayed amyloid-β-induced paralysis in the C. elegans model of Alzheimer's disease. Using a genetic approach, we found that DAF-16/FOXO transcription factor, heat shock factor 1, and SKN-1 (Nrf2 in mammals) were required for the extract-mediated delayed paralysis. The extract ameliorated oxidative stress by reducing the level of H2O2, which appeared to account for the protective action of the extract. The extract possesses antioxidant activity against juglone-induced oxidative stress as it was shown to increase survival of the stressed worms. In addition, C. formosum decreased the expression of the heat shock protein-16.2 gene which was induced by thermal stress, indicating its ability to reduce cellular stress. The results from this study support the C. elegans model in the search for disease-modifying agents to treat Alzheimer's disease and indicate the potential of the extract from C. formosum ssp. pruniflorum as a source for the development of anti-Alzheimer's drugs. © Georg Thieme Verlag KG Stuttgart · New York.
dc.subjectamyloid beta protein
dc.subjectascorbic acid
dc.subjectcaffeic acid
dc.subjectchlorogenic acid
dc.subjectCratoxylum formosum extract
dc.subjectgallic acid
dc.subjectGinkgo biloba extract
dc.subjectheat shock transcription factor 1
dc.subjecthydrogen peroxide
dc.subjectjuglone
dc.subjectneuroprotective agent
dc.subjectplant extract
dc.subjecttranscription factor FOXO
dc.subjecttranscription factor Nrf2
dc.subjectunclassified drug
dc.subjectamyloid beta protein
dc.subjectantioxidant
dc.subjectCaenorhabditis elegans protein
dc.subjectdaf-16 protein, C elegans
dc.subjectDNA binding protein
dc.subjectforkhead transcription factor
dc.subjectheat shock factor-1, C elegans
dc.subjectnaphthoquinone
dc.subjectplant extract
dc.subjectprotective agent
dc.subjectskn-1 protein, C elegans
dc.subjecttranscription factor
dc.subjectAlzheimer disease
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectCaenorhabditis elegans
dc.subjectcell stress
dc.subjectcontrolled study
dc.subjectCratoxylum formosum
dc.subjecthigh performance liquid chromatography
dc.subjectneuroprotection
dc.subjectneurotoxicity
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectparalysis
dc.subjectplant stem
dc.subjectplant twig
dc.subjectprotein expression
dc.subjectquantitative analysis
dc.subjectsurvival
dc.subjecttemperature stress
dc.subjecttransgenic animal
dc.subjectAlzheimer disease
dc.subjectanimal
dc.subjectCaenorhabditis elegans
dc.subjectchemistry
dc.subjectClusiaceae
dc.subjectdisease model
dc.subjectdrug effects
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectparalysis
dc.subjectAlzheimer Disease
dc.subjectAmyloid beta-Peptides
dc.subjectAnimals
dc.subjectAnimals, Genetically Modified
dc.subjectAntioxidants
dc.subjectCaenorhabditis elegans
dc.subjectCaenorhabditis elegans Proteins
dc.subjectClusiaceae
dc.subjectDisease Models, Animal
dc.subjectDNA-Binding Proteins
dc.subjectForkhead Transcription Factors
dc.subjectNaphthoquinones
dc.subjectOxidative Stress
dc.subjectParalysis
dc.subjectPlant Extracts
dc.subjectProtective Agents
dc.subjectTranscription Factors
dc.titleCratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationPlanta Medica. Vol 82, No.6 (2016), p.516-523
dc.identifier.doi10.1055/s-0041-111621
Appears in Collections:Scopus 1983-2021

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