Silent information regulator 1 protects the liver against ischemia-reperfusion injury: implications in steatotic liver ischemic preconditioning

被引:24
|
作者
Pantazi, Eirini [1 ,2 ]
Zaouali, Mohamed Amine [1 ,2 ,3 ]
Bejaoui, Mohamed [1 ,2 ]
Serafin, Anna [4 ]
Folch-Puy, Emma [1 ,2 ]
Petegnief, Valerie [5 ]
De Vera, Nuria [5 ]
Ben Abdennebi, Hassen [3 ]
Rimola, Antoni [2 ,6 ]
Rosello-Catafau, Joan [1 ,2 ]
机构
[1] CSIC, Inst Biomed Res Barcelona, IIBB, Expt Hepat Ischemia Reperfus Unit, Barcelona 08036, Catalonia, Spain
[2] Networked Biomed Res Ctr Hepat & Digest Dis Ciber, Barcelona, Catalonia, Spain
[3] Univ Monastir, Mol Biol & Anthropol Appl Dev & Hlth UR12ES11, Fac Pharm, Monastir, Tunisia
[4] Barcelona Sci Pk, Platform Lab Anim Appl Res, Barcelona, Catalonia, Spain
[5] CSIC, Dept Brain Ischemia & Neurodegenerat, IIBB, Inst Biomed Res Barcelona August Pi Sunyer, Barcelona 08036, Catalonia, Spain
[6] Hosp Clin Barcelona, Barcelona, Catalonia, Spain
关键词
ischemic preconditioning; Sirtuin; 1; nitric oxide; liver ischemia-reperfusion injury; oxidative stress; NF-KAPPA-B; FATTY LIVER; HISTONE DEACETYLASE; TRAUMA-HEMORRHAGE; OXIDATIVE STRESS; CELL-SURVIVAL; NITRIC-OXIDE; SIRT1; KINASE; TOLERANCE;
D O I
10.1111/tri.12276
中图分类号
R61 [外科手术学];
学科分类号
摘要
Ischemia-reperfusion (IR) injury is an important problem in liver surgery especially when steatosis is present. Ischemic preconditioning (PC) is the only surgical strategy that has been applied in patients with steatotic livers undergoing warm ischemia. Silent information regulator 1 (SIRT1) is a histone deacetylase that regulates various cellular processes. This study evaluates the SIRT1 implication in PC in fatty livers. Homozygous (Ob) Zucker rats were subjected to IR and IR+PC. An additional group treated with sirtinol or EX527 (SIRT1 inhibitors) before PC was also realized. Liver injury and oxidative stress were evaluated. SIRT1 protein levels and activity, as well as other parameters involved in PC protective mechanisms (adenosine monophosphate protein kinase, eNOS, HSP70, MAP kinases, apoptosis), were also measured. We demonstrated that the protective effect of PC was due in part to SIRT1 induction, as SIRT1 inhibition resulted in increased liver injury and abolished the beneficial mechanisms of PC. In this study, we report for the first time that SIRT1 is involved in the protective mechanisms induced by hepatic PC in steatotic livers.
引用
收藏
页码:493 / 503
页数:11
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