School of Biomedical Sciences and Pharmacy and Priority Research Centre for Stroke and Brain Injury, University of Newcastle, Callaghan, 2308, NSW, Australia.
Hunter Medical Research Institute, New Lambton Heights, 2305, NSW, Australia.
Transl Stroke Res. 2019 Aug;10(4):402-412. doi: 10.1007/s12975-018-0656-5. Epub 2018 Aug 28.
Low oxygen post conditioning (LOPC) has shown promising results in terms of neuroprotection after stroke, but the effects on motor function have not been considered. Cortical stroke targeting the motor and sensory cortex was induced by photothrombotic occlusion and after 48 h allocated to LOPC (11% O) for 2 weeks. Motor impairment was assessed using the cylinder and grid walk tests during the exposure period and for two further weeks upon completion of the intervention. Neuroprotection was evaluated by histological and molecular analysis at two time points. Two weeks of LOPC was sufficient to significantly reduce motor deficits and tissue loss after stroke. This functional improvement was associated with increased capillary density, enhanced levels of BDNF, decreased neuronal loss and decreased microglia activation. These improvements, in most instances, were maintained up to 2 weeks after the end of the treatment. To our knowledge, this is the first study to demonstrate that LOPC induces a persistent improvement in motor function and neuroprotection after stroke, and in doing so provides evidence to support a case for considering taking LOPC forward to early stage clinical research.
低氧后处理(LOPC)在卒中后神经保护方面显示出良好的效果,但对运动功能的影响尚未得到考虑。光血栓闭塞诱导大脑皮质卒中,靶向运动和感觉皮质,在 48 小时后将其分配到 LOPC(11% O)进行 2 周治疗。在暴露期间和干预完成后的两周内,使用圆筒和网格行走测试评估运动障碍。在两个时间点进行组织学和分子分析来评估神经保护。2 周的 LOPC 足以显著减少卒中后的运动缺陷和组织损失。这种功能改善与毛细血管密度增加、BDNF 水平升高、神经元丢失减少和小胶质细胞激活减少有关。在大多数情况下,这些改善在治疗结束后 2 周内仍然存在。据我们所知,这是第一项证明 LOPC 可在卒中后持续改善运动功能和神经保护的研究,因此为考虑将 LOPC 推进早期临床研究提供了证据支持。