Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12081
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dc.contributor.authorKeowkase R.
dc.contributor.authorKijmankongkul N.
dc.contributor.authorSangtian W.
dc.contributor.authorPoomborplab S.
dc.contributor.authorSanta-ardharnpreecha C.
dc.contributor.authorWeerapreeyakul N.
dc.contributor.authorSitthithaworn W.
dc.date.accessioned2021-04-05T03:01:51Z-
dc.date.available2021-04-05T03:01:51Z-
dc.date.issued2020
dc.identifier.issn1934578X
dc.identifier.other2-s2.0-85088094490
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12081-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85088094490&doi=10.1177%2f1934578X20933511&partnerID=40&md5=b51ba3a6221e9984e415672fa596daf4
dc.description.abstractAlzheimer’s disease (AD) is the most common form of dementia found in the elderly. AD is caused by the accumulation of toxic proteins including amyloid-β (Aβ). The purpose of this study was to investigate the effect of fruit extract of Aegle marmelos against Aβ toxicity in Caenorhabditis elegans. The fruit of A. marmelos has been used in a traditional Thai herb formula in fatigue patients recovering from illnesses such as fever and diarrhea. We used a transgenic C. elegans strain CL4176, which expresses the human Aβ42, to investigate the effects and the mechanisms of action of the extracts against Aβ toxicity. The extract of A. marmelos significantly delayed Aβ-induced paralysis. Aegle marmelos lost the ability to delay Aβ-induced paralysis in worms fed with daf-16 ribonucleic acid interference (RNAi) bacteria, but not in worms fed with hsf-1 and skin-1 RNAi bacteria. These results indicated that daf-16 transcription factor was required for A. marmelos-mediated delayed paralysis. Aegle marmelos enhanced the level of daf-16 gene. Taken together, these results indicated that A. marmelos reduced Aβ toxicity via the DAF-16-mediated cell signaling pathway. In addition, A. marmelos reduced toxic Aβ oligomers. Aegle marmelos also displayed antioxidative effect in in vivo as it enhanced resistance to paraquat-induced oxidative stress in wild type worms. All of the results suggested that A. marmelos can protect against Aβ-induced toxicity and can be a potential candidate for the prevention or treatment of AD. © The Author(s) 2020.
dc.subjectAegle marmelos extract
dc.subjectamyloid beta protein[25-35]
dc.subjectepigallocatechin gallate
dc.subjectoligomer
dc.subjectparaquat
dc.subjecttranscription factor DAF 16
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectCaenorhabditis elegans
dc.subjectcontrolled study
dc.subjectdrug effect
dc.subjectdrug mechanism
dc.subjectfruit
dc.subjecthigh performance liquid chromatography
dc.subjectin vivo study
dc.subjectneuroprotection
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectparalysis
dc.subjectprotein expression
dc.subjectRNA interference
dc.subjectsignal transduction
dc.subjecttransgenic animal
dc.subjectwild type
dc.titleProtective Effect and Mechanism of Fruit Extract of Aegle marmelos Against Amyloid-β Toxicity in a Transgenic Caenorhabditis elegans
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationNatural Product Communications. Vol 15, No.7 (2020)
dc.identifier.doi10.1177/1934578X20933511
Appears in Collections:Scopus 1983-2021

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