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Cited 9 time in webofscience Cited 11 time in scopus
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Role of Phytoconstituents as PPAR Agonists: Implications for Neurodegenerative Disorders

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dc.contributor.authorSanjay-
dc.contributor.authorSharma, Anshul-
dc.contributor.authorLee, Hae-Jeung-
dc.date.accessioned2022-01-07T01:40:39Z-
dc.date.available2022-01-07T01:40:39Z-
dc.date.created2022-01-07-
dc.date.issued2021-12-
dc.identifier.issn2227-9059-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/83150-
dc.description.abstractPeroxisome proliferator-activated receptors (PPAR-gamma, PPAR-alpha, and PPAR-beta/delta) are ligand-dependent nuclear receptors that play a critical role in the regulation of hundreds of genes through their activation. Their expression and targeted activation play an important role in the treatment of a variety of diseases, including neurodegenerative, cardiovascular, diabetes, and cancer. In recent years, several reviews have been published describing the therapeutic potential of PPAR agonists (natural or synthetic) in the disorders listed above; however, no comprehensive report defining the role of naturally derived phytoconstituents as PPAR agonists targeting neurodegenerative diseases has been published. This review will focus on the role of phytoconstituents as PPAR agonists and the relevant preclinical studies and mechanistic insights into their neuroprotective effects. Exemplary research includes flavonoids, fatty acids, cannabinoids, curcumin, genistein, capsaicin, and piperine, all of which have been shown to be PPAR agonists either directly or indirectly. Additionally, a few studies have demonstrated the use of clinical samples in in vitro investigations. The role of the fruit fly Drosophila melanogaster as a potential model for studying neurodegenerative diseases has also been highlighted.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.relation.isPartOfBIOMEDICINES-
dc.titleRole of Phytoconstituents as PPAR Agonists: Implications for Neurodegenerative Disorders-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000736171700001-
dc.identifier.doi10.3390/biomedicines9121914-
dc.identifier.bibliographicCitationBIOMEDICINES, v.9, no.12-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85123001480-
dc.citation.titleBIOMEDICINES-
dc.citation.volume9-
dc.citation.number12-
dc.contributor.affiliatedAuthorSanjay-
dc.contributor.affiliatedAuthorSharma, Anshul-
dc.contributor.affiliatedAuthorLee, Hae-Jeung-
dc.type.docTypeArticle-
dc.subject.keywordAuthorneurodegenerative disorders-
dc.subject.keywordAuthorPPARs-
dc.subject.keywordAuthorphytoconstituents-
dc.subject.keywordAuthorbioactivities-
dc.subject.keywordAuthoranti-inflammation-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorParkinson disease-
dc.subject.keywordAuthorHuntington disease-
dc.subject.keywordPlusPROLIFERATOR-ACTIVATED-RECEPTOR-
dc.subject.keywordPlusEXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS-
dc.subject.keywordPlusISCHEMIA-REPERFUSION INJURY-
dc.subject.keywordPlusPOLYUNSATURATED FATTY-ACIDS-
dc.subject.keywordPlusNUCLEAR HORMONE-RECEPTORS-
dc.subject.keywordPlusRETINOID-X-RECEPTORS-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusDOCOSAHEXAENOIC ACID-
dc.subject.keywordPlusGAMMA AGONISTS-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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