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dc.contributor.authorWantida Chaiyanaen_US
dc.contributor.authorChanun Punyoyaien_US
dc.contributor.authorSuvimol Somwonginen_US
dc.contributor.authorPimporn Leelapornpisiden_US
dc.contributor.authorKornkanok Ingkaninanen_US
dc.contributor.authorNeti Waranuchen_US
dc.contributor.authorJukkarin Srivilaien_US
dc.contributor.authorNatthawut Thitipramoteen_US
dc.contributor.authorWudtichai Wisuitiproten_US
dc.contributor.authorRoswitha Schusteren_US
dc.contributor.authorHelmut Viernsteinen_US
dc.contributor.authorMonika Muelleren_US
dc.date.accessioned2018-09-05T03:26:22Z-
dc.date.available2018-09-05T03:26:22Z-
dc.date.issued2017-10-10en_US
dc.identifier.issn20726643en_US
dc.identifier.other2-s2.0-85031304472en_US
dc.identifier.other10.3390/nu9101105en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85031304472&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56438-
dc.description.abstract© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This study aims to investigate the biological activities related to hair loss of Equisetum debile extracts, including 5α-reductase inhibition, interleukin-6 (IL-6) secretion reduction, and anti-oxidation. E. debile extracts were obtained by maceration in various solvents. Crude extract (CE) was obtained by maceration in 95% ethanol. Chlorophyll-free extract (CF) was the CE which of the chlorophyll has been removed by electrocoagulation. Hexane extract (HE), ethyl acetate extract (EA), and ethanolic extract (ET) were fraction extracts obtained from maceration in hexane, ethyl acetate, and 95% ethanol, respectively. The extracts were investigated for inhibitory activity against 5α-reductase and IL-6 secretion. Total phenolic contents (TPC) were investigated and antioxidant activities were determined by means of 2,20-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS), 2,20-diphenyl-1-picrylhydrazyl (DPPH), and ferric reducing antioxidant power (FRAP) assays. The inhibition of lipid peroxidation was determined by the ferric thiocyanate method. The cytotoxicity of the extracts on dermal papilla cells and irritation test by hen's egg test chorioallantoic membrane assay were also investigated. All extracts could inhibit 5α-reductase and decrease IL-6 secretion in lipopolysaccharide-stimulated macrophage. The antioxidant activity of E. debile extracts was directly related to their TPC. ET which contained the highest TPC (68.8 ± 6.7 mg GA/g) showed the highest equivalent concentration (EC1) of 289.1 ± 26.4 mM FeSO4/g, TEAC of 156.6 ± 34.6 mM Trolox/g, and 20.0 ± 6.0% DPPH inhibition. However, EA exhibited the highest inhibition against lipid peroxidation (57.2 ± 0.4%). In addition, EA showed no cytotoxicity on dermal papilla cell line and no irritation on chorioallantoic membrane of hen’s eggs. In conclusion, EA was suggested as the most attractive ingredients for functional food and nutraceuticals because of the high inhibitory activity against 5α-reductase, IL-6 secretion, and lipid peroxidation inhibition.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectNursingen_US
dc.titleInhibition of 5α-reductase, IL-6 secretion, and oxidation process of equisetum debile roxb. Ex vaucher extract as functional food and nutraceuticals ingredientsen_US
dc.typeJournalen_US
article.title.sourcetitleNutrientsen_US
article.volume9en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsNaresuan Universityen_US
article.stream.affiliationsMae Fah Luang Universityen_US
article.stream.affiliationsSirindhorn College of Public Healthen_US
article.stream.affiliationsUniversitat Wienen_US
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