León-Moreno Lilia Carolina, Castañeda-Arellano Rolando, Rivas-Carrillo Jorge David, Dueñas-Jiménez Sergio Horacio
Laboratory of Neurophysiology, Health Sciences Center, University de Guadalajara, Jalisco Mexico.
Department of Biomedical Sciences, University Center of Tonala, University de Guadalajara, Jalisco Mexico.
J Stroke Cerebrovasc Dis. 2020 May;29(5):104773. doi: 10.1016/j.jstrokecerebrovasdis.2020.104773. Epub 2020 Mar 19.
Brain ischemia is one of the principal causes of death and disability worldwide in which prevention or an effective treatment does not exist. In order to develop successful treatments, an adequate and useful ischemia model is essential. Transient global cerebral ischemia is one of the most interesting pathological conditions in stroke studies because of the observed degeneration of forebrain and delayed neuronal cell death in selective vulnerable regions such as hippocampus. Transient occlusion of both common carotid arteries is the most convenient model to induce tGCI. Although there are effective rat and gerbil models using this method, the induction of a reproducible and reliable injury after global ischemia in mouse has presented higher variations, mainly because of its size and the necessary monitoring skills in order to accomplish homogeneous and reproducible results. Further, great variability among cerebral vasculature and susceptibility of the different strains and sub-strains is observed. In recent years, some modifications have been made to the model in order to normalize the heterogenic effects. Analysis of posterior communicating artery patency has been proposed as an exclusion parameter due to the direct relationship reported with the reduction of cerebral blood flow. Another method used to significantly reduce blood flow is the induction of hypotension with isoflurane. Each protocol produces distinct injury outcomes. Further improvements are needed to attain a general, simpler, reproducible and globally accepted model that allows comparisons between research groups, progress in understanding ischemia and the consequent development of therapeutic alternatives for ischemic injury.
脑缺血是全球范围内导致死亡和残疾的主要原因之一,目前尚无预防或有效治疗方法。为了开发成功的治疗方法,建立一个合适且有用的缺血模型至关重要。短暂性全脑缺血是中风研究中最引人关注的病理状况之一,因为观察到前脑退化以及在海马等选择性易损区域出现延迟性神经元细胞死亡。双侧颈总动脉短暂闭塞是诱导短暂性全脑缺血最便捷的模型。尽管使用这种方法已有有效的大鼠和沙鼠模型,但在小鼠全脑缺血后诱导出可重复且可靠的损伤存在较大差异,主要是因为小鼠的体型以及为获得均匀且可重复的结果所需的监测技巧。此外,还观察到不同脑血循环以及不同品系和亚品系易感性之间存在很大差异。近年来,已对该模型进行了一些改进,以规范其异质性影响。由于后交通动脉通畅性与脑血流量减少之间存在直接关系,因此已提议将其作为一个排除参数进行分析。另一种用于显著减少血流量的方法是用异氟烷诱导低血压。每种方案都会产生不同的损伤结果。需要进一步改进,以获得一个通用、更简单、可重复且被全球接受的模型,以便不同研究小组之间进行比较,推动对缺血的理解,并由此开发针对缺血性损伤的治疗替代方案。