Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/77231
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFahsai Kantawongen_US
dc.contributor.authorChanakarn Saisuwanen_US
dc.contributor.authorPirakorn Soeratanapanten_US
dc.contributor.authorPhenphichar Wanachantararaken_US
dc.contributor.authorJiang Nanen_US
dc.contributor.authorJianming Wuen_US
dc.contributor.authorYoung Tae Changen_US
dc.date.accessioned2022-10-16T07:24:57Z-
dc.date.available2022-10-16T07:24:57Z-
dc.date.issued2021-01-01en_US
dc.identifier.issn17414288en_US
dc.identifier.issn1741427Xen_US
dc.identifier.other2-s2.0-85104179557en_US
dc.identifier.other10.1155/2021/8818618en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85104179557&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77231-
dc.description.abstractGynura divaricata (GD) is an Asian herb widely used as an alternative medicine and functional food for type 2 diabetes. Diabetic neuropathy is considered as an important complication of diabetic patients. This study focused on neuroregenerative effects of GD for use in the prevention of diabetic neuropathy. GD leaves were cut and boiled in water to mimic real-life cooking. The boiled content was filtered through white gauze and lyophilized to preserve as dried powder. Antioxidant assay was performed using DPPH assays. UHPLC-QTOF-MS/MS was employed to test for important compounds in the extract of these herbs. MTT assay was used to test for cell viability. The extracts at concentration of 250 μg/mL were tested with human gingival cell to observe the change of gene expression. The DPPH assay showed that GD water extract at the concentration of 5000 μg/mL could inhibit DPPH radical for 39.2%. The results showed that 5000 μg of GD water extract contained total phenolic content equivalent to 310.9 μg standard gallic acid. UHPLC-QTOF-MS/MS result found phenolic acids and flavonoids as the main components. Human gingival cells treated with 250 μg/mL of GD water extract for 10 days showed upregulation of some neuronal differentiation markers. Staining with Cdr3 dye confirmed the presentation of neuronal progenitors. The extract at the concentration of 250 μg/mL was also tested with apical papilla cells to screen for change of gene expression by RNA sequencing. The result also showed significant upregulation of alpha-internexin (INA). These results indicated that GD water extract might have an inductive effect for neural regeneration and could be used as functional food and supplementation for the prevention or treatment of diabetic neuropathy. This work provided the basic knowledge for further investigations into the benefits of GD for diabetic neuropathy.en_US
dc.subjectMedicineen_US
dc.titleGynura divaricata Water Extract Presented the Possibility to Enhance Neuronal Regenerationen_US
dc.typeJournalen_US
article.title.sourcetitleEvidence-based Complementary and Alternative Medicineen_US
article.volume2021en_US
article.stream.affiliationsInstitute for Basic Science, Daejeonen_US
article.stream.affiliationsPohang University of Science and Technologyen_US
article.stream.affiliationsLuzhou Medical Collegeen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.