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脾缺血预处理减轻大鼠肝脏缺血再灌注诱导的氧化应激。

Splenic ischemic preconditioning attenuates oxidative stress induced by hepatic ischemia-reperfusion in rats.

作者信息

Costa Caio César Chaves, Pereira Nathalia Gabay, Machado Anna Luiza Melo, Dórea Mariana Albuquerque, Cruz Rafaella Macêdo Monteiro da, Silva Renata Cunha, Domingues Robson José de Souza, Yasojima Edson Yuzur

机构信息

Graduate student, Faculty of Medicine, UEPA, Belem-PA, Brazil. Technical procedures, analysis and interpretation of data, manuscript preparation.

Fellow, Postgraduate Program in Surgery and Experimental Research, UEPA, Belem-PA, Brazil. Technical procedures, analysis and interpretation of data, manuscript preparation.

出版信息

Acta Cir Bras. 2019 Sep 16;34(7):e201900707. doi: 10.1590/s0102-865020190070000007.

DOI:10.1590/s0102-865020190070000007
PMID:31531528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6756009/
Abstract

PURPOSE

To evaluate the effects of splenic ischemic preconditioning (sIPC) on oxidative stress induced by hepatic ischemia-reperfusion in rats.

METHODS

Fifteen male Wistar rats were equally divided into 3 groups: SHAM, IRI and sIPC. Animals from IRI group were subjected to 45 minutes of partial liver ischemia (70%). In the sIPC group, splenic artery was clamped in 2 cycles of 5 min of ischemia and 5 min of reperfusion (20 min total) prior to hepatic ischemia. SHAM group underwent the same surgical procedures as in the remaining groups, but no liver ischemia or sIPC were induced. After 1h, hepatic and splenic tissue samples were harvested for TBARS, CAT, GPx and GSH-Rd measurement.

RESULTS

sIPC treatment significantly decreased both hepatic and splenic levels of TBARS when compared to IRI group (p<0.01). Furthermore, the hepatic and splenic activities of CAT, GPx and GSH- Rd were significantly higher in sIPC group than in IRI group.

CONCLUSION

sIPC was able to attenuate hepatic and splenic IRI-induced oxidative stress.

摘要

目的

评估脾脏缺血预处理(sIPC)对大鼠肝脏缺血再灌注诱导的氧化应激的影响。

方法

将15只雄性Wistar大鼠平均分为3组:假手术组(SHAM)、缺血再灌注组(IRI)和脾脏缺血预处理组(sIPC)。IRI组动物接受45分钟的部分肝脏缺血(70%)。在sIPC组中,在肝脏缺血前,脾脏动脉进行2个周期的夹闭,每个周期缺血5分钟,再灌注5分钟(共20分钟)。SHAM组接受与其他组相同的手术操作,但不诱导肝脏缺血或sIPC。1小时后,采集肝脏和脾脏组织样本,用于测量丙二醛(TBARS)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽还原酶(GSH-Rd)。

结果

与IRI组相比,sIPC治疗显著降低了肝脏和脾脏的TBARS水平(p<0.01)。此外,sIPC组肝脏和脾脏的CAT、GPx和GSH-Rd活性显著高于IRI组。

结论

sIPC能够减轻肝脏和脾脏缺血再灌注诱导的氧化应激。

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本文引用的文献

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Circ Res. 2018 Oct 26;123(10):1152-1163. doi: 10.1161/CIRCRESAHA.118.313859.
2
Renal ischemia-reperfusion injury attenuated by splenic ischemic preconditioning.脾缺血预处理减轻肾缺血再灌注损伤。
Eur Rev Med Pharmacol Sci. 2018 Apr;22(7):2134-2142. doi: 10.26355/eurrev_201804_14747.
3
ROS homeostasis, a key determinant in liver ischemic-preconditioning.活性氧(ROS)稳态是肝脏缺血预处理的关键决定因素。
Redox Biol. 2017 Aug;12:1020-1025. doi: 10.1016/j.redox.2017.04.036. Epub 2017 May 4.
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Role of spleen in hepatic ischemia reperfusion injury: Splenic congestion during ischemia accelerates leukocyte infiltration within the liver after reperfusion.脾脏在肝缺血再灌注损伤中的作用:缺血期间的脾充血会加速再灌注后肝脏内的白细胞浸润。
Hepatol Res. 2017 Mar;47(3):E132-E141. doi: 10.1111/hepr.12740. Epub 2016 Jun 18.
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Ischaemic conditioning and reperfusion injury.缺血预处理和再灌注损伤。
Nat Rev Cardiol. 2016 Apr;13(4):193-209. doi: 10.1038/nrcardio.2016.5. Epub 2016 Feb 4.
6
Reperfusion injury and reactive oxygen species: The evolution of a concept.再灌注损伤与活性氧:一个概念的演变
Redox Biol. 2015 Dec;6:524-551. doi: 10.1016/j.redox.2015.08.020. Epub 2015 Oct 8.
7
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Rodent models of hepatic ischemia-reperfusion injury: time and percentage-related pathophysiological mechanisms.肝缺血再灌注损伤的啮齿动物模型:与时间和百分比相关的病理生理学机制。
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