新生大鼠局灶性脑缺血的可重复性实验模型

Tong-Chun Wen , Marta Rogido , Pierre Gressens , Augusto Sola
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引用次数: 32

摘要

最近的数据表明,局灶性脑缺血(FCI)和中风的发生率比以前认识到的要高,并且可能占早产儿和足月新生儿脑病变的很大比例。因此,开发一种合适的新生动物FCI模型至关重要。我们在此描述了出生后第7天大鼠幼崽永久性FCI的改进模型(P7)。将不同直径(180 ~ 220 μm)的缝线栓子插入不同体重(14 ~ 19 g)幼犬的左颈总动脉(CCA),将缝线栓子推进至大脑中动脉(MCA),使其闭塞,形成永久性FCI。永久性FCI后立即用炭黑染色对连续脑切片的缺血区域进行成像,以评估血管闭塞的成功。永久性FCI 24 h后,2,3,5-三苯四氯唑(TTC)染色证实脑梗死一致。末端脱氧核苷酸转移酶介导的2 ' -脱氧尿苷5 ' -三磷酸生物素缺口末端标记(TUNEL)染色显示缺血区域细胞死亡,TUNEL标记是细胞凋亡的特征之一。目前的模型为新生儿FCI的高级病理生理学研究开辟了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A reproducible experimental model of focal cerebral ischemia in the neonatal rat

Recent data suggest that the incidence of focal cerebral ischemia (FCI) and stroke is higher than previously recognized and could account for a large proportion of brain lesions in the preterm and full term neonate. Therefore, it is critically important to develop an appropriate model of FCI in neonatal animals. We describe here a modified model of permanent FCI in rat pups at postnatal day-7 (P7). To produce permanent FCI, a suture embolus with different diameters (180–220 μm) was inserted into the left common carotid artery (CCA) of the pups with different weight (14–19 g). Then the suture embolus was advanced to the middle cerebral artery (MCA) to produce its occlusion. The success of vascular occlusion was evaluated by imaging the ischemic territory on serial brain sections with carbon black staining immediately after permanent FCI. The consistent cerebral infarction was confirmed by 2,3,5-triphenyltetrazolium chloride (TTC) staining 24 h after permanent FCI. Terminal deoxynucleotidyltransferase-mediated 2′-deoxyuridine 5′-triphospate-biotin nick end labeling (TUNEL) staining showed cell death with TUNEL labeling in the ischemic areas, which is one of the features of apoptosis. The present model opens the way for advanced pathophysiological studies of FCI in neonates.

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