Matches in SemOpenAlex for { <https://semopenalex.org/work/W2767679438> ?p ?o ?g. }
- W2767679438 endingPage "105629" @default.
- W2767679438 startingPage "105615" @default.
- W2767679438 abstract "// Chong Jie 1, 2 , Zhuo Luo 1, 2 , Huan Chen 1, 2 , Min Wang 3 , Chang Yan 1, 2 , Zhong-Fu Mao 1, 2 , Gao-Keng Xiao 2 , Hiroshi Kurihara 1, 2 , Yi-Fang Li 1, 2 and Rong-Rong He 1, 2 1 Anti-Stress and Health Research Center, College of Pharmacy, Jinan University, Guangzhou 510632, China 2 Institute of Traditional Chinese Medicine & Natural Products, Jinan University, Guangzhou 510632, China 3 Department of Pharmacy, Hainan General Hospital, Hainan 570311, China Correspondence to: Rong-Rong He, email: rongronghe@jnu.edu.cn Yi-Fang Li, email: liyifang706@jnu.edu.cn Hiroshi Kurihara, email: Kurihara_hiroshi@163.com Keywords: indirubin; influenza virus; virus susceptibility; MAVS; STING Received: February 25, 2017 Accepted: July 18, 2017 Published: November 09, 2017 ABSTRACT Isatis indigotica has a long history in treating virus infection and related symptoms in China. Nevertheless, its antivirus evidence in animal studies is not satisfactory, which might be due to the lack of appropriate animal model. Previously, we had utilized restraint stress to establish mouse H1N1 susceptibility model which was helpful in evaluating the anti-virus effect of medicines targeting host factors, such as type I interferon production. In this study, this model was employed to investigate the effect and mechanism of indirubin, a natural bisindole alkaloid from Isatis indigotica , on influenza A virus susceptibility. In the in vitro study, the stress hormone corticosterone was used to simulate restraint stress. Our results demonstrated that indirubin decreased the susceptibility to influenza virus with lowered mortality and alleviated lung damage in restraint-stressed mice model. Moreover, indirubin promoted the expression of interferon-β and interferon inducible transmembrane 3. In addition, indirubin maintained the morphology and function of mitochondria following influenza A virus infection. Further study revealed that indirubin promoted interferon-β production through promoting mitochondrial antiviral signaling pathway. Our study indicated that indirubin could be a candidate for the therapy of influenza." @default.
- W2767679438 created "2017-11-17" @default.
- W2767679438 creator A5007206077 @default.
- W2767679438 creator A5010282121 @default.
- W2767679438 creator A5015102287 @default.
- W2767679438 creator A5017108478 @default.
- W2767679438 creator A5026503460 @default.
- W2767679438 creator A5040189982 @default.
- W2767679438 creator A5067236490 @default.
- W2767679438 creator A5069593117 @default.
- W2767679438 creator A5087975581 @default.
- W2767679438 creator A5088519518 @default.
- W2767679438 date "2017-11-09" @default.
- W2767679438 modified "2023-10-18" @default.
- W2767679438 title "Indirubin, a bisindole alkaloid from <i>Isatis indigotica</i>, reduces H1N1 susceptibility in stressed mice by regulating MAVS signaling" @default.
- W2767679438 cites W1967900006 @default.
- W2767679438 cites W1968178474 @default.
- W2767679438 cites W1973610263 @default.
- W2767679438 cites W1974809008 @default.
- W2767679438 cites W1975461687 @default.
- W2767679438 cites W1976205207 @default.
- W2767679438 cites W1976372006 @default.
- W2767679438 cites W1978897742 @default.
- W2767679438 cites W1980931348 @default.
- W2767679438 cites W1988107639 @default.
- W2767679438 cites W1995510727 @default.
- W2767679438 cites W1995755756 @default.
- W2767679438 cites W1996311210 @default.
- W2767679438 cites W2003988251 @default.
- W2767679438 cites W2016676153 @default.
- W2767679438 cites W2031784540 @default.
- W2767679438 cites W2032725983 @default.
- W2767679438 cites W2033059529 @default.
- W2767679438 cites W2033448006 @default.
- W2767679438 cites W2034098922 @default.
- W2767679438 cites W2034322984 @default.
- W2767679438 cites W2038616986 @default.
- W2767679438 cites W2058607861 @default.
- W2767679438 cites W2069273876 @default.
- W2767679438 cites W2071688420 @default.
- W2767679438 cites W2072383590 @default.
- W2767679438 cites W2073234751 @default.
- W2767679438 cites W2073254057 @default.
- W2767679438 cites W2074974240 @default.
- W2767679438 cites W2077673494 @default.
- W2767679438 cites W2087241405 @default.
- W2767679438 cites W2087422295 @default.
- W2767679438 cites W2087668602 @default.
- W2767679438 cites W2091129202 @default.
- W2767679438 cites W2094323269 @default.
- W2767679438 cites W2104756450 @default.
- W2767679438 cites W2107513655 @default.
- W2767679438 cites W2109265999 @default.
- W2767679438 cites W2114421191 @default.
- W2767679438 cites W2115318272 @default.
- W2767679438 cites W2116498531 @default.
- W2767679438 cites W2118317431 @default.
- W2767679438 cites W2122399224 @default.
- W2767679438 cites W2137965676 @default.
- W2767679438 cites W2162835775 @default.
- W2767679438 cites W2163254642 @default.
- W2767679438 cites W2163496061 @default.
- W2767679438 cites W2163857054 @default.
- W2767679438 cites W2300023009 @default.
- W2767679438 cites W2336451601 @default.
- W2767679438 cites W2588862359 @default.
- W2767679438 doi "https://doi.org/10.18632/oncotarget.22350" @default.
- W2767679438 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5739664" @default.
- W2767679438 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29285277" @default.
- W2767679438 hasPublicationYear "2017" @default.
- W2767679438 type Work @default.
- W2767679438 sameAs 2767679438 @default.
- W2767679438 citedByCount "27" @default.
- W2767679438 countsByYear W27676794382018 @default.
- W2767679438 countsByYear W27676794382019 @default.
- W2767679438 countsByYear W27676794382020 @default.
- W2767679438 countsByYear W27676794382021 @default.
- W2767679438 countsByYear W27676794382022 @default.
- W2767679438 countsByYear W27676794382023 @default.
- W2767679438 crossrefType "journal-article" @default.
- W2767679438 hasAuthorship W2767679438A5007206077 @default.
- W2767679438 hasAuthorship W2767679438A5010282121 @default.
- W2767679438 hasAuthorship W2767679438A5015102287 @default.
- W2767679438 hasAuthorship W2767679438A5017108478 @default.
- W2767679438 hasAuthorship W2767679438A5026503460 @default.
- W2767679438 hasAuthorship W2767679438A5040189982 @default.
- W2767679438 hasAuthorship W2767679438A5067236490 @default.
- W2767679438 hasAuthorship W2767679438A5069593117 @default.
- W2767679438 hasAuthorship W2767679438A5087975581 @default.
- W2767679438 hasAuthorship W2767679438A5088519518 @default.
- W2767679438 hasBestOaLocation W27676794381 @default.
- W2767679438 hasConcept C185592680 @default.
- W2767679438 hasConcept C2777667214 @default.
- W2767679438 hasConcept C556039675 @default.
- W2767679438 hasConcept C71240020 @default.
- W2767679438 hasConcept C71924100 @default.
- W2767679438 hasConcept C98274493 @default.
- W2767679438 hasConceptScore W2767679438C185592680 @default.