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http://purl.uniprot.org/citations/23200736http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23200736http://www.w3.org/2000/01/rdf-schema#comment"Pro-inflammatory and pro-apoptotic mediators have been involved in the pathogenesis of neurodegenerative diseases. Tigecycline (Tig), a glycylcycline antibiotic and an analog of Minocycline, is shown to exert anti-inflammatory effects that are distinct from its anti-microbial activity. Its neuroprotective mechanism is unknown. In this study, we investigated the direct protective mechanisms of tigecycline against lipopolysaccharide (LPS)-induced Rat pheochromocytoma (PC12) cells. The results showed that tigecycline significantly attenuated the expression and the release of nuclear factor-kappa beta (NF-κB), tumor necrosis factor-alpha (TNF-α) and interleukin-1beta (IL-1β), as well as nitric oxide (NO) levels in LPS-induced PC12 cells. In addition, tigecycline dose-dependently decreased cytochrome c release and caspase-3 activity. This later finding corroborated the results of decreased pro-apoptotic Bad, and increased anti-apoptotic Bcl-2 protein expression thus, confirming a neuroprotective effect of the drug in differentiated PC12 cells induced with LPS. The findings of our study suggest new targets for tigecycline and support the potential for tigecycline to be investigated as a therapeutic agent for neurodegenerative disorders."xsd:string
http://purl.uniprot.org/citations/23200736http://purl.org/dc/terms/identifier"doi:10.1016/j.tiv.2012.11.015"xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/author"Benzeroual K.E."xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/author"Yagnik R.M."xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/name"Toxicol In Vitro"xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/pages"686-693"xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/title"Tigecycline prevents LPS-induced release of pro-inflammatory and apoptotic mediators in neuronal cells."xsd:string
http://purl.uniprot.org/citations/23200736http://purl.uniprot.org/core/volume"27"xsd:string
http://purl.uniprot.org/citations/23200736http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23200736
http://purl.uniprot.org/citations/23200736http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23200736
http://purl.uniprot.org/uniprot/Q63264#attribution-EAC6B9BC4F2827F58BC490E52B4B47B1http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/#_A0A8I6A5V4-mappedCitation-23200736http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/#_Q5BKB0-mappedCitation-23200736http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/#_Q63264-mappedCitation-23200736http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/Q63264http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/A0A8I6A5V4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23200736
http://purl.uniprot.org/uniprot/Q5BKB0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23200736