Ren Xiaoping, Wang Yang, Jones W Keith
Department of Pharmacology and Cell Biophysics, University of Cincinnati, 231 Albert Sabin Way, Cincinnati, OH 45267-0575, USA.
J Surg Res. 2004 Sep;121(1):120-9. doi: 10.1016/j.jss.2004.03.010.
Ischemic preconditioning (IPC) and remote IPC are cardioprotective phenomena in which ischemia of the myocardium or of a remote tissue, respectively, induces cardioprotection. Despite clinical evidence that surgical trauma can remotely affect myocardial infarction, to date there are no basic science studies addressing the effect of nonischemic trauma at distant sites upon cardiac ischemia/reperfusion (I/R) injury. The objectives of this study were to determine the effects of nonischemic remote surgical trauma upon infarct size after myocardial I/R and to determine the effects of TNF-alpha ablation upon cardioprotective phenomena.
A minimally traumatic mouse model was used to ascertain the effect of remote nonischemic surgical trauma upon I/R injury. TNF-alpha knockout mice were employed to determine the effect of TNF-alpha ablation.
Carotid artery vascular surgery remotely exacerbates cardiac I/R injury increasing infarct size by 287% (remote cardiac injury or RCI). Nonischemic, nonvascular trauma (abdominal incision) results in remote preconditioning of trauma (RPCT), decreasing infarct size by 81% (early phase) and 40% (late phase) relative to controls. Finally, TNF-alpha is required for late IPC but is not necessary for RCI or for RPCT.
We show that late IPC is TNF-alpha-dependent and describe two unique TNF-alpha-independent remote effects of nonischemic trauma upon myocardial infarction. Understanding the mechanism of these remote effects will allow the development of novel therapies for the treatment of ischemic heart disease. RPCT and TNF-alpha ablation have an additive protective effect suggesting that combinations of complementary approaches may be a useful strategy for maximizing the clinical efficacy of cardioprotective therapies.
缺血预处理(IPC)和远程缺血预处理是心脏保护现象,分别是指心肌或远程组织的缺血诱导心脏保护作用。尽管有临床证据表明手术创伤可对心肌梗死产生远程影响,但迄今为止,尚无基础科学研究探讨远处非缺血性创伤对心脏缺血/再灌注(I/R)损伤的影响。本研究的目的是确定非缺血性远程手术创伤对心肌I/R后梗死面积的影响,并确定肿瘤坏死因子-α(TNF-α)消融对心脏保护现象的影响。
使用微创小鼠模型确定远程非缺血性手术创伤对I/R损伤的影响。采用TNF-α基因敲除小鼠确定TNF-α消融的影响。
颈动脉血管手术可远程加重心脏I/R损伤,使梗死面积增加287%(远程心脏损伤或RCI)。非缺血性非血管创伤(腹部切口)可导致创伤的远程预处理(RPCT),相对于对照组,梗死面积在早期减少81%,在晚期减少40%。最后,晚期IPC需要TNF-α,但RCI或RPCT则不需要。
我们发现晚期IPC依赖于TNF-α,并描述了非缺血性创伤对心肌梗死的两种独特的不依赖TNF-α的远程效应。了解这些远程效应的机制将有助于开发治疗缺血性心脏病的新疗法。RPCT和TNF-α消融具有相加的保护作用,提示互补方法的联合可能是最大化心脏保护疗法临床疗效的有用策略。