Sheldon R A, Chuai J, Ferriero D M
Department of Neurology, University of California San Francisco 94143-0114, USA.
Biol Neonate. 1996;69(5):327-41. doi: 10.1159/000244327.
We proposed that hypoxic-ischemic injury suffered on postnatal day 1 (P1) in the newborn rat would yield significant and reproducible brain injury simulating that seen in a midgestation human brain. The P1 pup was subjected to ipsilateral common carotid ligation followed by 3.5 h of 6% O2 and demonstrated consistent histological changes in the ipsilateral hemisphere. At P2 neuronal loss and edema were pronounced in cortex and caudate; edema subsequently declined by P3. Astrocytic and microglial reactivity were seen as early as 24 h after injury, and by P10 both were extensive in damaged areas. There was marked loss of white matter on the affected side. We have demonstrated a reproducible model of hypoxic-ischemic injury to the very immature brain that can be used to elucidate mechanisms of neuronal loss and periventricular leukomalacia.
我们提出,新生大鼠出生后第1天(P1)遭受的缺氧缺血性损伤会导致显著且可重复的脑损伤,模拟中期妊娠人类大脑所见的损伤。对P1幼崽进行同侧颈总动脉结扎,随后置于6%氧气环境中3.5小时,同侧半球出现了一致的组织学变化。在P2时,皮质和尾状核出现明显的神经元丢失和水肿;水肿在P3时随后消退。早在损伤后24小时就可见星形胶质细胞和小胶质细胞反应,到P10时,受损区域两者都广泛存在。患侧白质有明显丢失。我们已经证明了一种可重复的极不成熟脑缺氧缺血性损伤模型,可用于阐明神经元丢失和脑室周围白质软化的机制。