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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/23803
Title: Carnosic acid protects SH-SY5Y cells against 6-hydroxydopamine-induced cell death through upregulation of parkin pathway
Authors: Lin, Chia-Yuan 
Tsai, Chia-Wen
Tsai, Chia-Wen
Keywords: Carnosic acid;Neuroprotection;Parkin;Ubiquitin-proteasomal system;alpha-synuclein;OXIDATIVE STRESS;MITOCHONDRIAL DYSFUNCTION;PROTEASOME;UBIQUITIN;BRAIN;PROTEINS;ROSEMARY;EXTRACT;PINK1;CONSTITUENTS
Issue Date: Nov-2016
Publisher: ELSEVIER
Journal Volume: 110
Journal Issue: Pt A
Source: Neuropharmacology
Abstract: 
Parkin is a Parkinson's disease (PD)-linked gene that plays an important role in the ubiquitin-proteasome system (UPS). This study explored whether carnosic acid (CA) from rosemary protects against 6-hydroxydopamine (6-OHDA)-induced neurotoxicity via upregulation of parkin in vivo and in vitro. We found that the reduction in proteasomal activity by 6-OHDA was attenuated in SH-SY5Y cells pretreated with 1 μM CA. Immunoblots showed that CA reversed the induction of ubiquitinated protein and the reduction of PTEN-induced putative kinase 1 (PINK1) and parkin protein in 6-OHDA-treated SH-SY5Y cells and rats. Moreover, in a transgenic OW13 Caenorhabditis elegans model of PD that expresses human α-synuclein in muscle cells, CA reduced α-synuclein accumulation in a dose-dependent manner. In cells pretreated with the proteasome inhibitor MG132, CA no longer reversed the 6-OHDA-mediated induction of cleavage of caspase 3 and poly(ADP)-ribose polymerase and no longer reversed the suppression of proteasome activity. When parkin expression was silenced by use of small interfering RNA, the ability of CA to inhibit apoptosis and induce proteasomal activity was significantly reduced. The reduction in 6-OHDA-induced neurotoxicity by CA was associated with the induction of parkin, which in turn upregulated the UPS and then decreased cell death.
URI: http://scholars.ntou.edu.tw/handle/123456789/23803
ISSN: 00283908
DOI: 10.1016/j.neuropharm.2016.04.017
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