Fasting protects liver from ischemic injury through Sirt1-mediated downregulation of circulating HMGB1 in mice

被引:94
|
作者
Rickenbacher, Andreas [1 ]
Jang, Jae Hwi [1 ]
Limani, Perparim [1 ]
Ungethuem, Udo [1 ]
Lehmann, Kuno [1 ]
Oberkofler, Christian E. [1 ]
Weber, Achim [2 ]
Graf, Rolf [1 ]
Humar, Bostjan [1 ]
Cavien, Pierre-Alain [1 ]
机构
[1] Univ Zurich Hosp, Dept Surg, Swiss Hepatopancreaticobiliary Ctr, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Inst Pathol, CH-8091 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Innate immunity; Anti-inflammatory; Liver ischemia; Kupffer cell; Autophagy; HMGB1; Sirtuin; Fasting; GROUP BOX 1; REPERFUSION INJURY; CALORIE RESTRICTION; DIETARY RESTRICTION; KUPFFER CELLS; MOUSE-LIVER; CHEMOKINE PRODUCTION; HISTONE DEACETYLASE; MYOCARDIAL-ISCHEMIA; HEPATIC ISCHEMIA;
D O I
10.1016/j.jhep.2014.04.010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Fasting and calorie restriction are associated with a prolonged life span and an increased resistance to stress. The protective effects of fasting have been exploited for the mitigation of ischemic organ injury, yet the underlying mechanisms remain incompletely understood. Here, we investigated whether fasting protects liver against ischemia reperfusion (IR) through energy-preserving or anti-inflammatory mechanisms. Methods: Fasted C57BL6 mice were subjected to partial hepatic IR. Injury was assessed by liver enzymes and histology. Raw264-7 macrophage-like cells were investigated in vitro. Sirt1 and HMGB1 were inhibited using Ex527 and neutralizing antibodies, respectively. Results: Fasting for one, but not two or three days, protected from hepatic IR injury. None of the investigated energy parameters correlated with the protective effects. Instead, inflammatory responses were dampened in one-day-fasted mice and in starved macrophages. Fasting alone led to a reduction in circulating HMGB1 associated with cytoplasmic HMGB1 translocation, aggregate formation, and autophagy. Inhibition of autophagy re-elevated circulating HMGB1 and abolished protection in fasted mice, as did supplementation with HMGB1. In vitro, Sirt1 inhibition prevented HMGB1 translocation, leading to elevated HMGB1 in the supernatant. In vivo, Sirt1 inhibition abrogated the fasting-induced protection, but had no effect in the presence of neutralizing HMGB1 antibody. Conclusions: Fasting for one day protects from hepatic IR injury via Sirt1-dependent downregulation of circulating HMGB1. The reduction in serum HMGB1 appears to be mediated by its engagement in the autophagic response. These findings integrate Sirt1, HMGB1, and autophagy into a common framework that underlies the anti-inflammatory properties of short-term fasting. (C) 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:301 / 308
页数:8
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