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本文引用的文献

1
Oxidative stress is fundamental to hyperbaric oxygen therapy.氧化应激是高压氧治疗的基础。
J Appl Physiol (1985). 2009 Mar;106(3):988-95. doi: 10.1152/japplphysiol.91004.2008. Epub 2008 Oct 9.
2
Marginal grafts increase early mortality in liver transplantation.边缘性移植物会增加肝移植术后的早期死亡率。
Sao Paulo Med J. 2008 May 1;126(3):161-5. doi: 10.1590/s1516-31802008000300005.
3
The effect of hyperbaric oxygen treatment on postoperative morbidity of left lobe donor in living donor adult liver transplantation.高压氧治疗对成人活体肝移植左叶供体术后发病率的影响。
Hepatogastroenterology. 2008 May-Jun;55(84):1014-9.
4
The evolution of liver transplantation practices.肝移植实践的演变。
Curr Opin Organ Transplant. 2008 Jun;13(3):275-9. doi: 10.1097/MOT.0b013e3282ffabee.
5
Actin S-nitrosylation inhibits neutrophil beta2 integrin function.肌动蛋白S-亚硝基化抑制中性粒细胞β2整合素功能。
J Biol Chem. 2008 Apr 18;283(16):10822-34. doi: 10.1074/jbc.M709200200. Epub 2008 Feb 18.
6
Hyperbaric oxygen improves capillary morphology in severe acute pancreatitis.高压氧可改善重症急性胰腺炎的毛细血管形态。
Pancreas. 2008 Jan;36(1):70-5. doi: 10.1097/mpa.0b013e3181485863.
7
Beneficial effects of hyperbaric oxygen pretreatment on massive hepatectomy model in rats.高压氧预处理对大鼠大面积肝切除模型的有益作用。
Transplantation. 2007 Dec 27;84(12):1656-61. doi: 10.1097/01.tp.0000291778.86758.1d.
8
Glycine reduces hepatic warm ischaemia-reperfusion injury by suppressing inflammatory reactions in rats.甘氨酸通过抑制大鼠的炎症反应减轻肝脏热缺血再灌注损伤。
Liver Int. 2007 Nov;27(9):1249-54. doi: 10.1111/j.1478-3231.2007.01564.x.
9
Absence of toll-like receptor 4 (TLR4) signaling in the donor organ reduces ischemia and reperfusion injury in a murine liver transplantation model.在小鼠肝移植模型中,供体器官中Toll样受体4(TLR4)信号的缺失可减轻缺血再灌注损伤。
Liver Transpl. 2007 Oct;13(10):1435-43. doi: 10.1002/lt.21251.
10
Chemokines in ischemia and reperfusion.缺血再灌注中的趋化因子。
Thromb Haemost. 2007 May;97(5):738-47.

高压氧疗法可减轻肝移植大鼠模型缺血、保存和再灌注损伤的严重程度。

Hyperbaric oxygen therapy reduces the severity of ischaemia, preservation and reperfusion injury in a rat model of liver transplantation.

机构信息

Department of Surgery, The University of Melbourne, Austin Health, Studley Road, Heidelberg, Victoria, Australia.

出版信息

HPB (Oxford). 2012 Feb;14(2):103-14. doi: 10.1111/j.1477-2574.2011.00410.x. Epub 2011 Nov 13.

DOI:10.1111/j.1477-2574.2011.00410.x
PMID:22221571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3277052/
Abstract

BACKGROUND

Approaches to increase organ availability for orthotopic liver transplantation (OLT) often result in the procurement of marginal livers that are more susceptible to ischaemia, preservation and reperfusion injury (IPRI).

METHODS

The effects of post-OLT hyperbaric oxygen (HBO) therapy on IPRI in a syngeneic rat OLT model were examined at various time-points. The effects of IPRI and HBO on hepatocyte necrosis, apoptosis, proliferation, and sinusoidal morphology and ultrastructure were assessed.

RESULTS

Post-OLT HBO therapy significantly reduced the severity of IPRI; both apoptosis [at 12 h: 6.4 ± 0.4% in controls vs. 1.6 ± 0.7% in the HBO treatment group (p < 0.001); at 48 h: 2.4 ± 0.2% in controls vs. 0.4 ± 0.1% in the HBO treatment group (p < 0.001)] and necrosis [at 12 h: 18.7 ± 1.8% in controls vs. 2.4 ± 0.4% in the HBO treatment group (p < 0.001); at 48 h: 8.5 ± 1.3% in controls vs. 3.4 ± 0.9% in the HBO treatment group (P= 0.019)] were decreased. Serum alanine transaminase was reduced [at 12 h: 1068 ± 920 IU/l in controls vs. 370 ± 63 IU/l in the HBO treatment group (P= 0.030); at 48 h: 573 ± 261 IU/l in controls vs. 160 ± 10 IU/l in the HBO treatment group (P= 0.029)]. Treatment with HBO also promoted liver regeneration [proliferation at 12 h: 4.5 ± 0.1% in controls vs. 1.0 ± 0.3% in the HBO treatment group (p < 0.001); at 48 h: 8.6 ± 0.7% in controls vs. 2.9 ± 0.2% in the HBO treatment group (p < 0.01)] and improved sinusoidal diameter and microvascular density index.

CONCLUSIONS

Hyperbaric oxygen therapy has persistent positive effects post-OLT that may potentially transfer into clinical practice.

摘要

背景

为增加用于原位肝移植 (OLT) 的供体器官,常需获取边缘供肝,这些供肝更易发生缺血、保存和再灌注损伤 (IPRI)。

方法

本研究在同种异体大鼠 OLT 模型中,检测 OLT 后高压氧 (HBO) 治疗对 IPRI 的影响,并在不同时间点进行评估。检测 IPRI 和 HBO 对肝细胞坏死、凋亡、增殖以及窦状隙形态和超微结构的影响。

结果

OLT 后 HBO 治疗可显著减轻 IPRI 严重程度;凋亡[12 h:对照组为 6.4±0.4%,HBO 治疗组为 1.6±0.7%(p<0.001);48 h:对照组为 2.4±0.2%,HBO 治疗组为 0.4±0.1%(p<0.001)]和坏死[12 h:对照组为 18.7±1.8%,HBO 治疗组为 2.4±0.4%(p<0.001);48 h:对照组为 8.5±1.3%,HBO 治疗组为 3.4±0.9%(P=0.019)]均减少。血清丙氨酸转氨酶降低[12 h:对照组为 1068±920 IU/l,HBO 治疗组为 370±63 IU/l(p=0.030);48 h:对照组为 573±261 IU/l,HBO 治疗组为 160±10 IU/l(p=0.029)]。HBO 治疗还促进肝再生[12 h:对照组为 4.5±0.1%,HBO 治疗组为 1.0±0.3%(p<0.001);48 h:对照组为 8.6±0.7%,HBO 治疗组为 2.9±0.2%(p<0.01)],改善窦状隙直径和微血管密度指数。

结论

OLT 后 HBO 治疗具有持续的积极作用,可能转化为临床实践。