Literature DB >> 29870680

Hypothermic oxygenated perfusion (HOPE) attenuates ischemia/reperfusion injury in the liver through inhibition of the TXNIP/NLRP3 inflammasome pathway in a rat model of donation after cardiac death.

Weiyang He1, Shaojun Ye1, Cheng Zeng1, Shuai Xue1, Xiaoyan Hu1, Xingjian Zhang1, Siqi Gao1, Yan Xiong1, Xueyu He1, Soatina Vivalda1, Ling Li1, Yanfeng Wang1, Qifa Ye1,2.   

Abstract

Hypothermic oxygenated perfusion (HOPE) is a relatively new dynamic preservation procedure that has not been widely implemented in liver transplantation despite its advantages. Improved graft protection is one such advantage offered by HOPE and has been attributed to multiple mechanisms, one of which may be the modulation of the thioredoxin-interacting protein (TXNIP)/NOD-like receptor protein 3 (NLRP3) inflammasome pathway. The TXNIP/NLRP3 inflammasome pathway plays a critical role in sterile inflammation under oxidative stress as a result of ischemia/reperfusion injury (IRI). In the current study, we aimed to investigate the graft protection offered by HOPE and its impact on the TXNIP/NLRP3 inflammasome pathway. To simulate conditions of donation after cardiac death (DCD) liver transplantation, rat livers were exposed to 30 min of warm ischemia after cardiac arrest. Livers were then preserved under cold storage (CS) or with HOPE for 3 h. Livers were then subjected to 1 h of isolated reperfusion. Liver injuries were assessed on the isolated perfusion rat liver model system before and after reperfusion. Compared with the CS group, the HOPE group had a significant reduction in liver injury and improvement in liver function. Our findings also revealed that reperfusion injury induced liver damage and activated the TXNIP/NLRP3 inflammasome pathway in DCD rat livers. Pretreatment of DCD rat livers with HOPE inhibited the TXNIP/NLRP3 inflammasome pathway and attenuated liver IRI. Attenuation of oxidative stress as a result of HOPE led to the down-regulation of the TXNIP/NLRP3 inflammasome pathway and thus offered superior protection compared with the traditional CS method of organ preservation.-He, W., Ye, S., Zeng, C., Xue, S., Hu, X., Zhang, X., Gao, S., Xiong, Y., He, X., Vivalda, S., Li, L., Wang, Y., Ye, Q. Hypothermic oxygenated perfusion (HOPE) attenuates ischemia/reperfusion injury in the liver through inhibition of the TXNIP/NLRP3 inflammasome pathway in a rat model of donation after cardiac death.

Entities:  

Keywords:  flow stimulation; liver transplantation; organ preservation; sterile inflammation

Year:  2018        PMID: 29870680     DOI: 10.1096/fj.201800028RR

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  4 in total

Review 1.  The Role of NLRP3 Inflammasome Activation Pathway of Hepatic Macrophages in Liver Ischemia-Reperfusion Injury.

Authors:  Tong Wu; Cheng Zhang; Tianfeng Shao; Jianzhong Chen; Diyu Chen
Journal:  Front Immunol       Date:  2022-06-10       Impact factor: 8.786

2.  The long non-coding RNA H19 induces hypoxia/reoxygenation injury by up-regulating autophagy in the hepatoma carcinoma cells.

Authors:  Chao Cui; Zhiyu Li; Dequan Wu
Journal:  Biol Res       Date:  2019-06-13       Impact factor: 5.612

3.  Hypothermic oxygenated perfusion inhibits HECTD3-mediated TRAF3 polyubiquitination to alleviate DCD liver ischemia-reperfusion injury.

Authors:  Shaojun Ye; Qifa Ye; Wei Zhou; Zibiao Zhong; Danni Lin; Zhongzhong Liu; Qiuyan Zhang; Haoyang Xia; Sheng Peng; Anxiong Liu; Zhongshan Lu; Yanfeng Wang
Journal:  Cell Death Dis       Date:  2021-02-24       Impact factor: 8.469

Review 4.  Inflammasome-Mediated Inflammation in Liver Ischemia-Reperfusion Injury.

Authors:  Mónica B Jiménez-Castro; María Eugenia Cornide-Petronio; Jordi Gracia-Sancho; Carmen Peralta
Journal:  Cells       Date:  2019-09-23       Impact factor: 6.600

  4 in total

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