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DC Field | Value | Language |
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dc.contributor.author | Keowkase R. | |
dc.contributor.author | Weerapreeyakul N. | |
dc.date.accessioned | 2021-04-05T03:23:58Z | - |
dc.date.available | 2021-04-05T03:23:58Z | - |
dc.date.issued | 2016 | |
dc.identifier.issn | 320943 | |
dc.identifier.other | 2-s2.0-84957705999 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13442 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957705999&doi=10.1055%2fs-0041-111621&partnerID=40&md5=f95aef1b53bfd998cad65a62d7349375 | |
dc.description.abstract | Amyloid-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.subject | amyloid beta protein | |
dc.subject | ascorbic acid | |
dc.subject | caffeic acid | |
dc.subject | chlorogenic acid | |
dc.subject | Cratoxylum formosum extract | |
dc.subject | gallic acid | |
dc.subject | Ginkgo biloba extract | |
dc.subject | heat shock transcription factor 1 | |
dc.subject | hydrogen peroxide | |
dc.subject | juglone | |
dc.subject | neuroprotective agent | |
dc.subject | plant extract | |
dc.subject | transcription factor FOXO | |
dc.subject | transcription factor Nrf2 | |
dc.subject | unclassified drug | |
dc.subject | amyloid beta protein | |
dc.subject | antioxidant | |
dc.subject | Caenorhabditis elegans protein | |
dc.subject | daf-16 protein, C elegans | |
dc.subject | DNA binding protein | |
dc.subject | forkhead transcription factor | |
dc.subject | heat shock factor-1, C elegans | |
dc.subject | naphthoquinone | |
dc.subject | plant extract | |
dc.subject | protective agent | |
dc.subject | skn-1 protein, C elegans | |
dc.subject | transcription factor | |
dc.subject | Alzheimer disease | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | antioxidant activity | |
dc.subject | Article | |
dc.subject | Caenorhabditis elegans | |
dc.subject | cell stress | |
dc.subject | controlled study | |
dc.subject | Cratoxylum formosum | |
dc.subject | high performance liquid chromatography | |
dc.subject | neuroprotection | |
dc.subject | neurotoxicity | |
dc.subject | nonhuman | |
dc.subject | oxidative stress | |
dc.subject | paralysis | |
dc.subject | plant stem | |
dc.subject | plant twig | |
dc.subject | protein expression | |
dc.subject | quantitative analysis | |
dc.subject | survival | |
dc.subject | temperature stress | |
dc.subject | transgenic animal | |
dc.subject | Alzheimer disease | |
dc.subject | animal | |
dc.subject | Caenorhabditis elegans | |
dc.subject | chemistry | |
dc.subject | Clusiaceae | |
dc.subject | disease model | |
dc.subject | drug effects | |
dc.subject | genetics | |
dc.subject | metabolism | |
dc.subject | paralysis | |
dc.subject | Alzheimer Disease | |
dc.subject | Amyloid beta-Peptides | |
dc.subject | Animals | |
dc.subject | Animals, Genetically Modified | |
dc.subject | Antioxidants | |
dc.subject | Caenorhabditis elegans | |
dc.subject | Caenorhabditis elegans Proteins | |
dc.subject | Clusiaceae | |
dc.subject | Disease Models, Animal | |
dc.subject | DNA-Binding Proteins | |
dc.subject | Forkhead Transcription Factors | |
dc.subject | Naphthoquinones | |
dc.subject | Oxidative Stress | |
dc.subject | Paralysis | |
dc.subject | Plant Extracts | |
dc.subject | Protective Agents | |
dc.subject | Transcription Factors | |
dc.title | Cratoxylum formosum Extract Protects against Amyloid-Beta Toxicity in a Caenorhabditis elegans Model of Alzheimer's Disease | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Planta Medica. Vol 82, No.6 (2016), p.516-523 | |
dc.identifier.doi | 10.1055/s-0041-111621 | |
Appears in Collections: | Scopus 1983-2021 |
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