| Literature DB >> 26671127 |
Yin-Zhong Ma1, Li Li1, Jun-Ke Song1, Zi-Ran Niu1, Hai-Feng Liu2, Xiang-Shan Zhou3, Fu-Sheng Xie4, Guan-Hua Du5.
Abstract
Stroke is a major cause of death and disability worldwide. However, treatment options to date are very limited. To meet the need for validating the novel therapeutic approaches and understanding the physiopathology of the ischemic brain injury, experimental stroke models were critical for preclinical research. However, commonly used embolic stroke models are reluctant to mimic the clinical situation and not suitable for thrombolytic timing studies. In this paper, we established a standard method for producing a rat embolic stroke model with autologous thrombus formed within the common carotid artery (CCA) by constant galvanic stimulation. Then the thrombus was shattered and channeled into the origin of the MCA and small (lacunar) artery. To identify the success of MCA occlusion, regional cerebral blood flow was monitored, neurological deficits and infarct volumes were measured at 2, 4 and 6h postischemia. This model developed a predictable infarct volume (38.37 ± 2.88%) and gradually reduced blood flow (20% of preischemic baselines) within the middle cerebral artery (MCA) territory. The thrombus occluded in the MCA was able to be lysed by a tissue-type plasminogen activator (t-PA) within 4h postischemia. The techniques presented in this paper would help investigators to overcome technical problems for stroke research.Entities:
Keywords: Cerebral embolism; Disease model; Stroke; Therapeutic time window; Thrombolytic; t-PA
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Year: 2015 PMID: 26671127 DOI: 10.1016/j.jns.2015.09.362
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181