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dc.contributor.authorXia, Baomei
dc.contributor.authorTong, Yue
dc.contributor.authorXia, Changbo
dc.contributor.authorChen, Chang
dc.contributor.authorShan, Xin
dc.date.accessioned2021-01-13T01:59:07Z
dc.date.available2021-01-13T01:59:07Z
dc.date.issued2020-10-08
dc.identifier.citationXia, B., Tong, Y., Xia, C., Chen, C., & Shan, X. (2020). α-Cyperone Confers Antidepressant-Like Effects in Mice via Neuroplasticity Enhancement by SIRT3/ROS Mediated NLRP3 Inflammasome Deactivation. Frontiers in Pharmacology, 11, 1625.en_US
dc.identifier.issn1663-9812
dc.identifier.pmid33132912
dc.identifier.doi10.3389/fphar.2020.577062
dc.identifier.urihttp://hdl.handle.net/10150/650741
dc.description.abstractalpha-Cyperone (Cy) is a major active compound of Cyperus rotundus that has various pharmacological activities. But whether Cy possesses antidepressant effect is unknown. In this study, we exposed mice to chronic unpredictable mild stress (CUMS) with or without intervention with Cy. Our results showed that Cy significantly improved the depressive phenotypes in sucrose preference test, tail suspension test and forced swimming test. Meanwhile, increased SIRT3 expression, reduced ROS production and activated NF-kappa B signal were detected in the hippocampus of mice. NLRP3 inflammasome related proteins including NLRP3, ASC, Caspase-1, IL-1 beta, IL-18 and GSDMD-N were downregulated after Cy administration. Synaptic proteins including Synapsin-1 and PSD-95 and dendritic spine density were improved after Cy treatment. Moreover, the protective effects of Cy in CUMS mice were compromised when co-administrated with SIRT3 inhibitor 3-TYP. Taken together, these findings suggested that Cy has therapeutic potential for treating depression and that this antidepressant effect may be attributed to SIRT3 stimulated neuroplasticity enhancement by suppressing NLRP3 inflammasome.en_US
dc.language.isoenen_US
dc.publisherFRONTIERS MEDIA SAen_US
dc.rightsCopyright © 2020 Xia, Tong, Xia, Chen and Shan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.subjectdepressionen_US
dc.subjectSIRT3en_US
dc.subjectROSen_US
dc.subjectNLRP3 inflammasomeen_US
dc.subjectneuroplasticityen_US
dc.subjectalpha-cyperoneen_US
dc.subjectα-cyperoneen_US
dc.titleα-Cyperone Confers Antidepressant-Like Effects in Mice Neuroplasticity Enhancement by SIRT3/ROS Mediated NLRP3 Inflammasome Deactivationen_US
dc.typeArticleen_US
dc.contributor.departmentUniv Arizona, Coll Med Phoenix, Dept Basic Med Scien_US
dc.identifier.journalFRONTIERS IN PHARMACOLOGYen_US
dc.description.noteOpen access journalen_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal published versionen_US
dc.source.journaltitleFrontiers in pharmacology
dc.source.volume11
dc.source.beginpage577062
dc.source.endpage
refterms.dateFOA2021-01-13T01:59:09Z
dc.source.countrySwitzerland


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Copyright © 2020 Xia, Tong, Xia, Chen and Shan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
Except where otherwise noted, this item's license is described as Copyright © 2020 Xia, Tong, Xia, Chen and Shan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).