Ren Changhong, Wang Pengcheng, Wang Brian, Li Ning, Li Weiguang, Zhang Chenggang, Jin Kunlin, Ji Xunming
Institute of Hypoxia Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China.
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center at Fort Worth, Texas, USA.
Restor Neurol Neurosci. 2015;33(3):369-79. doi: 10.3233/RNN-140413.
Limb remote ischemic per-conditioning or post-conditioning has been shown to be neuroprotective after cerebral ischemic stroke. However, the effect of combining remote per-conditioning with post-conditioning on ischemic/reperfusion injury as well as the underlying mechanisms are largely unexplored.
Here, adult male Sprague Dawley rats were subjected to middle cerebral artery occlusion (MCAO). The limb ischemic stimulus was immediately applied after onset of focal ischemia (per-conditioning), followed by repeated short episodes of remote ischemia 24 hr after reperfusion (post-conditioning). The infarct volume, motor function, and the expression of neuroglobin (Ngb) were measured at different durations after reperfusion.
We found that a single episode of limb remote per-conditioning afforded short-term protection, but combining repeated remote post-conditioning during the 14 days after reperfusion significantly ameliorated cerebral ischemia/reperfusion injury. Interestingly, we also found that ischemic per- and post-conditioning significantly increased expression of Ngb, an oxygen-binding globin protein that has been demonstrated to be neuroprotective against stroke, at peri-infarct regions from day 1 to day 14 following ischemia/reperfusion.
Our results suggest that the conventional per-conditioning combined with post-conditioning may be used as a novel neuroprotective strategy against ischemia-reperfusion injury, and Ngb seems to be one of the important players in limb remote ischemia-mediated neuroprotection.
肢体远程缺血预处理或后处理已被证明在脑缺血性中风后具有神经保护作用。然而,将远程预处理与后处理相结合对缺血/再灌注损伤的影响及其潜在机制在很大程度上尚未得到探索。
在此,成年雄性Sprague Dawley大鼠接受大脑中动脉闭塞(MCAO)。在局灶性缺血发作后立即施加肢体缺血刺激(预处理),然后在再灌注后24小时重复进行短暂的远程缺血发作(后处理)。在再灌注后的不同时间段测量梗死体积、运动功能和神经球蛋白(Ngb)的表达。
我们发现单次肢体远程预处理提供了短期保护,但在再灌注后的14天内结合重复的远程后处理可显著改善脑缺血/再灌注损伤。有趣的是,我们还发现缺血预处理和后处理在缺血/再灌注后的第1天至第14天显著增加了梗死周围区域Ngb的表达,Ngb是一种氧结合球蛋白,已被证明对中风具有神经保护作用。
我们的结果表明,传统的预处理与后处理相结合可作为一种针对缺血再灌注损伤的新型神经保护策略,并且Ngb似乎是肢体远程缺血介导的神经保护中的重要参与者之一。