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10.1038/srep25042

http://scihub22266oqcxt.onion/10.1038/srep25042
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C4858649!4858649!27150843
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suck abstract from ncbi


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pmid27150843      Sci+Rep 2016 ; 6 (ä): ä
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  • Baicalein pretreatment reduces liver ischemia/reperfusion injury via induction of autophagy in rats #MMPMID27150843
  • Liu A; Huang L; Guo E; Li R; Yang J; Li A; Yang Y; Liu S; Hu J; Jiang X; Dirsch O; Dahmen U; Sun J
  • Sci Rep 2016[]; 6 (ä): ä PMID27150843show ga
  • We previously demonstrated that baicalein could protect against liver ischemia/reperfusion (I/R) injury in mice. The exact mechanism of baicalein remains poorly understood. Autophagy plays an important role in protecting against I/R injury. This study was designed to determine whether baicalein could protect against liver I/R injury via induction of autophagy in rats. Baicalein was intraperitoneally injected 1?h before warm ischemia. Pretreatment with baicalein prior to I/R insult significantly blunted I/R-induced elevations of serum aminotransferase levels and significantly improved the histological status of livers. Electron microscopy and expression of the autophagic marker LC3B-II suggested induction of autophagy after baicalein treatment. Moreover, inhibition of the baicalein-induced autophagy using 3-methyladenine (3-MA) worsened liver injury. Furthermore, baicalein treatment increased heme oxygenase (HO)-1 expression, and pharmacological inhibition of HO-1 with tin protoporphyrin IX (SnPP) abolished the baicalein-mediated autophagy and the hepatocellular protection. In primary rat hepatocytes, baicalein-induced autophagy also protected hepatocytes from hypoxia/reoxygenation injury in vitro and the beneficial effect was abrogated by 3-MA or Atg7 siRNA, respectively. Suppression of HO-1 activity by SnPP or HO-1 siRNA prevented the baicalein-mediated autophagy and resulted in increased hepatocellular injury. Collectively, these results suggest that baicalein prevents hepatocellular injury via induction of HO-1-mediated autophagy.
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