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Matrix Metalloproteinase-9 Production following Cardiopulmonary Bypass Was Not Associated with Pulmonary Dysfunction after Cardiac Surgery.体外循环后基质金属蛋白酶-9的产生与心脏手术后的肺功能障碍无关。
Mediators Inflamm. 2015;2015:341740. doi: 10.1155/2015/341740. Epub 2015 Jul 27.
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Synergistic suppressive effect of PARP-1 inhibitor PJ34 and HDAC inhibitor SAHA on proliferation of liver cancer cells.PARP-1抑制剂PJ34与HDAC抑制剂SAHA对肝癌细胞增殖的协同抑制作用
J Huazhong Univ Sci Technolog Med Sci. 2015 Aug;35(4):535-540. doi: 10.1007/s11596-015-1466-6. Epub 2015 Jul 31.
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EFFECT OF RELATIVE GENE EXPRESSION ON PLAQUE VULNERABILITY IN PATIENTS WITH STABLE ANGINA AND PATIENTS WITH ACUTE CORONARY SYNDROME.相对基因表达对稳定型心绞痛患者和急性冠状动脉综合征患者斑块易损性的影响。
J Biol Regul Homeost Agents. 2015 Apr-Jun;29(2):437-41.
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Angiotensin II induces an increase in MMP-2 expression in idiopathic ascending aortic aneurysm via AT1 receptor and JNK pathway.血管紧张素II通过AT1受体和JNK途径诱导特发性升主动脉瘤中MMP-2表达增加。
Acta Biochim Biophys Sin (Shanghai). 2015 Jul;47(7):539-47. doi: 10.1093/abbs/gmv047. Epub 2015 Jun 11.
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Deficiency of MMP17/MT4-MMP proteolytic activity predisposes to aortic aneurysm in mice.MMP17/MT4-MMP 蛋白水解活性缺乏可导致小鼠发生主动脉瘤。
Circ Res. 2015 Jul 3;117(2):e13-26. doi: 10.1161/CIRCRESAHA.117.305108. Epub 2015 May 11.
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A Meta-Analysis of Renal Function After Adult Cardiac Surgery With Pulsatile Perfusion.成人心脏手术搏动灌注后肾功能的Meta分析。
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Non-healing foot ulcers in diabetic patients: general and local interfering conditions and management options with advanced wound dressings.糖尿病患者足部溃疡不愈合:全身及局部干扰因素及使用先进伤口敷料的管理方案
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Organ-protective effects on the liver and kidney by minocycline in small piglets undergoing cardiopulonary bypass.米诺环素对接受体外循环的小猪肝脏和肾脏的器官保护作用。
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体外循环期间针对缺血-再灌注损伤的药理学器官保护策略。

Strategies for Pharmacological Organoprotection during Extracorporeal Circulation Targeting Ischemia-Reperfusion Injury.

作者信息

Salameh Aida, Dhein Stefan

机构信息

Clinic for Pediatric Cardiology, Heart Centre University of Leipzig Leipzig, Germany.

Rudolf-Boehm-Institute for Pharmacology and Toxicology, University of Leipzig Leipzig, Germany.

出版信息

Front Pharmacol. 2015 Dec 22;6:296. doi: 10.3389/fphar.2015.00296. eCollection 2015.

DOI:10.3389/fphar.2015.00296
PMID:26733868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4686733/
Abstract

Surgical correction of congenital cardiac malformations or aortocoronary bypass surgery in many cases implies the use of cardiopulmonary-bypass (CPB). However, a possible negative impact of CPB on internal organs such as brain, kidney, lung and liver cannot be neglected. In general, CPB initiates a systemic inflammatory response (SIRS) which is presumably caused by contact of blood components with the surface of CPB tubing. Moreover, during CPB the heart typically undergoes a period of cold ischemia, and the other peripheral organs a global low flow hypoperfusion. As a result, a plethora of pro-inflammatory mediators and cytokines is released activating different biochemical pathways, which finally may result in the occurrence of microthrombosis, microemboli, in depletion of coagulation factors and haemorrhagic diathesis besides typical ischemia-reperfusion injuries. In our review we will focus on possible pharmacological interventions in patients to decrease negative effects of CPB and to improve post-operative outcome with regard to heart and other organs like brain, kidney, or lung.

摘要

在许多情况下,先天性心脏畸形的外科矫正或主动脉冠状动脉搭桥手术都需要使用体外循环(CPB)。然而,CPB对诸如脑、肾、肺和肝脏等内部器官可能产生的负面影响不容忽视。一般来说,CPB会引发全身炎症反应(SIRS),这可能是由血液成分与CPB管道表面接触引起的。此外,在CPB期间,心脏通常会经历一段冷缺血期,而其他外周器官则会出现全身性低流量灌注不足。结果,大量促炎介质和细胞因子被释放,激活不同的生化途径,最终除了典型的缺血再灌注损伤外,还可能导致微血栓形成、微栓塞、凝血因子耗竭和出血素质的发生。在我们的综述中,我们将重点关注针对患者的可能的药物干预措施,以减少CPB的负面影响,并改善心脏以及脑、肾或肺等其他器官的术后结果。