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dc.creatorHung, Shih-Ya
dc.creatorChung, Hsin-Yi
dc.creatorLuo, Sih-Ting
dc.creatorChu, Yu-Ting
dc.creatorChen, Yu-Hsin
dc.creatorMacDonald, Iona J.
dc.creatorChien, Szu-Yu
dc.creatorKotha, Peddanna
dc.creatorYang, Liang-Yo
dc.creatorHwang, Ling-Ling
dc.creatorDun, Nae J.
dc.creatorChuang, De-Maw
dc.creatorChen, Yi-Hung
dc.date.accessioned2024-03-13T20:23:50Z
dc.date.available2024-03-13T20:23:50Z
dc.date.issued2022-08-09
dc.identifier.citationHung S-Y, Chung H-Y, Luo S-T, Chu Y-T, Chen Y-H, MacDonald IJ, Chien S-Y, Kotha P, Yang L-Y, Hwang L-L, Dun NJ, Chuang D-M and Chen Y-H (2022) Electroacupuncture improves TBI dysfunction by targeting HDAC overexpression and BDNF-associated Akt/GSK-3β signaling. Front. Cell. Neurosci. 16:880267. doi: 10.3389/fncel.2022.880267
dc.identifier.issn1662-5102
dc.identifier.urihttp://hdl.handle.net/20.500.12613/9858
dc.description.abstractBackground: Acupuncture or electroacupuncture (EA) appears to be a potential treatment in acute clinical traumatic brain injury (TBI); however, it remains uncertain whether acupuncture affects post-TBI histone deacetylase (HDAC) expression or impacts other biochemical/neurobiological events. Materials and methods: We used behavioral testing, Western blot, and immunohistochemistry analysis to evaluate the cellular and molecular effects of EA at LI4 and LI11 in both weight drop-impact acceleration (WD)- and controlled cortical impact (CCI)-induced TBI models. Results: Both WD- and CCI-induced TBI caused behavioral dysfunction, increased cortical levels of HDAC1 and HDAC3 isoforms, activated microglia and astrocytes, and decreased cortical levels of BDNF as well as its downstream mediators phosphorylated-Akt and phosphorylated-GSK-3β. Application of EA reversed motor, sensorimotor, and learning/memory deficits. EA also restored overexpression of HDAC1 and HDAC3, and recovered downregulation of BDNF-associated signaling in the cortex of TBI mice. Conclusion: The results strongly suggest that acupuncture has multiple benefits against TBI-associated adverse behavioral and biochemical effects and that the underlying mechanisms are likely mediated by targeting HDAC overexpression and aberrant BDNF-associated Akt/GSK-3 signaling.
dc.format.extent23 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofFaculty/ Researcher Works
dc.relation.haspartFrontiers in Cellular Neuroscience, Vol. 16
dc.relation.isreferencedbyFrontiers Media
dc.rightsAttribution CC BY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectElectroacupuncture
dc.subjectPreclinical traumatic brain injury
dc.subjectMotor function tests
dc.subjectHistone deacetylases
dc.subjectBDNF
dc.subjectAkt/GSK-3β
dc.titleElectroacupuncture improves TBI dysfunction by targeting HDAC overexpression and BDNF-associated Akt/GSK-3β signaling
dc.typeText
dc.type.genreJournal article
dc.description.departmentMedicine
dc.relation.doihttp://dx.doi.org/10.3389/fncel.2022.880267
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeLewis Katz School of Medicine
dc.temple.creatorDun, Nae J.
refterms.dateFOA2024-03-13T20:23:50Z


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