Publication:
Cratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease

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.date.issuedBE2559
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.format.mimetypeapplication/pdf
dc.identifier.citationPlanta Medica. Vol 82, No.6 (2016), p.516-523
dc.identifier.doi10.1055/s-0041-111621
dc.identifier.issn320943
dc.identifier.other2-s2.0-84957705999
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5486
dc.rights.holderScopus
dc.subject.otherAmyloid beta protein
dc.subject.otherAscorbic acid
dc.subject.otherCaffeic acid
dc.subject.otherChlorogenic acid
dc.subject.otherCratoxylum formosum extract
dc.subject.otherGallic acid
dc.subject.otherGinkgo biloba extract
dc.subject.otherHeat shock transcription factor 1
dc.subject.otherHydrogen peroxide
dc.subject.otherJuglone
dc.subject.otherNeuroprotective agent
dc.subject.otherPlant extract
dc.subject.otherTranscription factor FOXO
dc.subject.otherTranscription factor Nrf2
dc.subject.otherUnclassified drug
dc.subject.otherAmyloid beta protein
dc.subject.otherAntioxidant
dc.subject.otherCaenorhabditis elegans protein
dc.subject.otherDaf-16 protein, C elegans
dc.subject.otherDNA binding protein
dc.subject.otherForkhead transcription factor
dc.subject.otherHeat shock factor-1, C elegans
dc.subject.otherNaphthoquinone
dc.subject.otherPlant extract
dc.subject.otherProtective agent
dc.subject.otherSkn-1 protein, C elegans
dc.subject.otherTranscription factor
dc.subject.otherAlzheimer disease
dc.subject.otherAnimal experiment
dc.subject.otherAnimal model
dc.subject.otherAnimal tissue
dc.subject.otherAntioxidant activity
dc.subject.otherArticle
dc.subject.otherCaenorhabditis elegans
dc.subject.otherCell stress
dc.subject.otherControlled study
dc.subject.otherCratoxylum formosum
dc.subject.otherHigh performance liquid chromatography
dc.subject.otherNeuroprotection
dc.subject.otherNeurotoxicity
dc.subject.otherNonhuman
dc.subject.otherOxidative stress
dc.subject.otherParalysis
dc.subject.otherPlant stem
dc.subject.otherPlant twig
dc.subject.otherProtein expression
dc.subject.otherQuantitative analysis
dc.subject.otherSurvival
dc.subject.otherTemperature stress
dc.subject.otherTransgenic animal
dc.subject.otherAlzheimer disease
dc.subject.otherAnimal
dc.subject.otherCaenorhabditis elegans
dc.subject.otherChemistry
dc.subject.otherClusiaceae
dc.subject.otherDisease model
dc.subject.otherDrug effects
dc.subject.otherGenetics
dc.subject.otherMetabolism
dc.subject.otherParalysis
dc.subject.otherAlzheimer Disease
dc.subject.otherAmyloid beta-Peptides
dc.subject.otherAnimals
dc.subject.otherAnimals, Genetically Modified
dc.subject.otherAntioxidants
dc.subject.otherCaenorhabditis elegans
dc.subject.otherCaenorhabditis elegans Proteins
dc.subject.otherClusiaceae
dc.subject.otherDisease Models, Animal
dc.subject.otherDNA-Binding Proteins
dc.subject.otherForkhead Transcription Factors
dc.subject.otherNaphthoquinones
dc.subject.otherOxidative Stress
dc.subject.otherParalysis
dc.subject.otherPlant Extracts
dc.subject.otherProtective Agents
dc.subject.otherTranscription Factors
dc.titleCratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84957705999&doi=10.1055%2fs-0041-111621&partnerID=40&md5=f95aef1b53bfd998cad65a62d7349375

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