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本文引用的文献

1
Anesthetic propofol reduces endotoxic inflammation by inhibiting reactive oxygen species-regulated Akt/IKKβ/NF-κB signaling.麻醉性 propofol 通过抑制活性氧调节的 Akt/IKKβ/NF-κB 信号通路减轻内毒素性炎症。
PLoS One. 2011 Mar 8;6(3):e17598. doi: 10.1371/journal.pone.0017598.
2
Propofol infusion syndrome: update of clinical manifestation and pathophysiology.丙泊酚输注综合征:临床表现与病理生理学的更新
Minerva Anestesiol. 2009 May;75(5):339-44.
3
Propofol infusion syndrome.丙泊酚输注综合征
J Trauma Nurs. 2008 Jul-Sep;15(3):118-22. doi: 10.1097/01.JTN.0000337153.08464.0f.
4
Persistent depression of contractility and vasodilation with propofol but not with sevoflurane or desflurane in rabbits.兔体内,丙泊酚可使收缩力持续降低并引起血管舒张,而七氟烷或地氟烷则不会。
Anesthesiology. 2008 Jan;108(1):87-93. doi: 10.1097/01.anes.0000296077.32685.26.
5
Propofol infusion syndrome.丙泊酚输注综合征
Anaesthesia. 2007 Jul;62(7):690-701. doi: 10.1111/j.1365-2044.2007.05055.x.
6
Anti-inflammatory and antioxidative effects of propofol on lipopolysaccharide-activated macrophages.丙泊酚对脂多糖激活的巨噬细胞的抗炎和抗氧化作用。
Ann N Y Acad Sci. 2005 May;1042:262-71. doi: 10.1196/annals.1338.030.
7
Propofol is cardioprotective in a clinically relevant model of normothermic blood cardioplegic arrest and cardiopulmonary bypass.在常温血液心脏停搏和体外循环的临床相关模型中,丙泊酚具有心脏保护作用。
Exp Biol Med (Maywood). 2005 Jun;230(6):413-20. doi: 10.1177/15353702-0323006-09.
8
The effects of propofol on lipid peroxidation and inflammatory response in elective coronary artery bypass grafting.丙泊酚对择期冠状动脉旁路移植术中脂质过氧化和炎症反应的影响。
J Cardiothorac Vasc Anesth. 2004 Oct;18(5):592-604. doi: 10.1053/j.jvca.2004.07.018.
9
Antioxidative effect of propofol during cardiopulmonary bypass in adults.丙泊酚在成人体外循环期间的抗氧化作用。
Acta Pharmacol Sin. 2004 Mar;25(3):334-40.
10
The pathophysiology of propofol infusion syndrome: a simple name for a complex syndrome.丙泊酚输注综合征的病理生理学:一个复杂综合征的简单名称。
Intensive Care Med. 2003 Sep;29(9):1417-25. doi: 10.1007/s00134-003-1905-x. Epub 2003 Aug 6.

丙泊酚在体外循环期间的抗炎作用:一项初步研究。

Anti-inflammatory effects of propofol during cardiopulmonary bypass: a pilot study.

作者信息

Samir A, Gandreti N, Madhere M, Khan A, Brown M, Loomba V

机构信息

Department of Anesthesia, Henry Ford Hospital, Detroit, Michigan, USA.

出版信息

Ann Card Anaesth. 2015 Oct-Dec;18(4):495-501. doi: 10.4103/0971-9784.166451.

DOI:10.4103/0971-9784.166451
PMID:26440235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4881689/
Abstract

INTRODUCTION

Propofol has been suggested as a useful adjunct to cardiopulmonary bypass (CPB) because of its potential protective effect on the heart mediated by a decrease in ischemia-reperfusion injury and inflammation at clinically relevant concentrations. In view of these potentially protective properties, which modulate many of the deleterious mechanism of inflammation attributable to reperfusion injury and CPB, we sought to determine whether starting a low dose of propofol infusion at the beginning of CPB would decrease inflammation as measured by pro-inflammatory markers.

MATERIALS AND METHODS

We enrolled 24 patients undergoing elective coronary artery bypass graft (CABG). The study group received propofol at rate of 120 mcg/kg/min immediately after starting CPB and was maintained throughout the surgery and for the following 6 hours in the intensive care unit (ICU). The control group received propofol dose of 30-50 mcg/kg/min which was started at the time of chest closure with wires and continued for the next 6 hours in the ICU. Interleukins (IL) -6, -8 and -10 and tumor necrosis factor alpha (TNFalpha) were assayed.

RESULT

The most significant difference was in the level of IL-6 which had a P value of less than 0.06. Starting a low dose propofol early during the CPB was not associated with significant hemodynamic instability in comparison with the control group.

CONCLUSION

Our study shows that propofol may be suitable as an anti-inflammatory adjunct for patients undergoing CABG.

摘要

引言

丙泊酚已被认为是体外循环(CPB)的一种有用辅助药物,因为在临床相关浓度下,它对心脏具有潜在的保护作用,可通过减少缺血再灌注损伤和炎症来介导。鉴于这些潜在的保护特性,其可调节许多由再灌注损伤和CPB引起的有害炎症机制,我们试图确定在CPB开始时开始低剂量丙泊酚输注是否会如通过促炎标志物所测量的那样减少炎症。

材料与方法

我们纳入了24例接受择期冠状动脉旁路移植术(CABG)的患者。研究组在CPB开始后立即以120 mcg/kg/min的速率接受丙泊酚,并在整个手术过程中以及在重症监护病房(ICU)接下来的6小时内持续使用。对照组在胸部用钢丝闭合时开始接受30 - 50 mcg/kg/min的丙泊酚剂量,并在ICU中持续使用接下来的6小时。检测白细胞介素(IL)-6、-8和-10以及肿瘤坏死因子α(TNFα)。

结果

最显著的差异在于IL-6水平,其P值小于0.06。与对照组相比,在CPB早期开始低剂量丙泊酚与显著的血流动力学不稳定无关。

结论

我们的研究表明,丙泊酚可能适合作为接受CABG患者的抗炎辅助药物。