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未成熟大鼠中度缺氧缺血后迟发性脑萎缩

Delayed cerebral atrophy following moderate hypoxia-ischemia in the immature rat.

作者信息

Geddes R, Vannucci R C, Vannucci S J

机构信息

Department of Neuroscience and Anatomy, Hershey Medical Center/Pennsylvania State University College of Medicine, Hershey, Pa 17033, USA.

出版信息

Dev Neurosci. 2001;23(3):180-5. doi: 10.1159/000046140.

Abstract

Hypoxia-ischemia (H/I) damages cells in the immature brain and interferes with subsequent brain development; the extent of the damage has been related to the severity, or duration, of the initial insult. This study examined the effects of both severe and moderate duration of H/I on the evolution of damage through 8 weeks of recovery. Seven-day-old rat pups were subjected to either 75 min or 2 h of 8% oxygen following a unilateral carotid artery ligation. Evaluation of brain damage included morphometric analysis of hemispheric diameter at 2, 4, and 8 weeks of recovery, and hematoxylin and eosin for evaluation of pathology at 8 weeks. Two hours of H/I produced severe infarction in the ipsilateral hemisphere in the majority of the survivors, apparent by 2 weeks of recovery with no change at 4 or 8 weeks. In marked contrast, 75 min of H/I produced no significant damage during the initial 2 weeks of recovery but resulted in progressive cerebral atrophy with delayed infarction such that the extent of damage at 8 weeks was not different from the 2-hour group. Thus, even a mild-moderate ischemic insult to the perinatal brain establishes a vulnerable region which ultimately dies without intervention.

摘要

缺氧缺血(H/I)会损害未成熟大脑中的细胞,并干扰随后的大脑发育;损伤程度与最初损伤的严重程度或持续时间有关。本研究通过8周的恢复期,考察了H/I严重和中等持续时间对损伤演变的影响。对7日龄幼鼠进行单侧颈动脉结扎后,使其暴露于8%氧气环境中75分钟或2小时。脑损伤评估包括在恢复2周、4周和8周时对半球直径进行形态计量分析,以及在8周时用苏木精和伊红染色评估病理学情况。2小时的H/I使大多数存活者的同侧半球出现严重梗死,在恢复2周时明显可见,在4周或8周时无变化。与之形成显著对比的是,75分钟的H/I在恢复的最初2周内未产生明显损伤,但导致进行性脑萎缩并伴有延迟性梗死,以至于8周时的损伤程度与2小时组无异。因此,即使是对围产期大脑的轻度至中度缺血性损伤也会形成一个易损区域,若不进行干预,该区域最终会死亡。

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