| Literature DB >> 29700717 |
Hongyu Xie1,2, Kewei Yu1,2, Naiyun Zhou3, Xueyan Shen1,2, Shan Tian1,2, Bei Zhang1,2, Yuyang Wang1,2, Junfa Wu1,2, Gang Liu1,2, Congyu Jiang1,2, Ruiping Hu1,2, Cenk Ayata4, Yi Wu5,6.
Abstract
Brain has limited capacity for spontaneous recovery of lost function after stroke. Exposure to enriched environment (EE) can facilitate functional recovery, but mechanisms underlying this effect are poorly understood. Here, we used a middle cerebral artery occlusion (MCAO) model to investigate the impact of EE on angiogenesis in the post-ischemic brain in adult male Sprague Dawley rats, and examined whether blood-borne factors may contribute. Compared with standard cage (SC), exposure to EE was associated with greater improvement in neurological function, higher peri-infarct vascular density, and higher chronic post-ischemic cerebral blood flow assessed by laser speckle imaging. The effect persisted for at least 28 days. EE also enhanced the expression of hepatocyte growth factor in the peri-ischemic cortex when measured 15 days after MCAO. Interestingly, serum from rats exposed to EE after MCAO showed elevated levels of hepatocyte growth factor, and plasma or serum from rats exposed to EE after MCAO enhanced the survival and proliferation of cultured endothelial cells, in vitro, when compared with control plasma or serum from SC group after MCAO. Together, our data suggest that exposure to EE promotes angiogenesis in the ischemic brain that may in part be mediated by blood-borne factors.Entities:
Keywords: Angiogenesis; Cerebral blood flow; Cerebral ischemia; Enriched environment; Hepatocyte growth factor
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Year: 2018 PMID: 29700717 DOI: 10.1007/s12975-018-0629-8
Source DB: PubMed Journal: Transl Stroke Res ISSN: 1868-4483 Impact factor: 6.829