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MK-801对新生大鼠新皮质冷冻损伤诱导的小回形成的神经保护作用。

The neuroprotective effects of MK-801 on the induction of microgyria by freezing injury to the newborn rat neocortex.

作者信息

Rosen G D, Sigel E A, Sherman G F, Galaburda A M

机构信息

Dyslexia Research Laboratory, Beth Israel Hospital, Boston, MA 02215, USA.

出版信息

Neuroscience. 1995 Nov;69(1):107-14. doi: 10.1016/0306-4522(95)00262-h.

Abstract

Four-layered microgyria is associated with many developmental disorders, including mental retardation, epilepsy, and developmental dyslexia. Freezing lesions to the newborn rodent neocortex result in the formation of four-layered microgyria. Previous research had suggested this type of injury acts as an hypoxic/ischemic event to the developing cortical plate. The current study examines the effectiveness of the non-competitive N-methyl-D-aspartate receptor antagonist dizocilpine (MK-801) in protecting against freezing injury to the newborn rat cortical plate. Three groups of rats received freezing injury to the cortical plate on the first day of life (postnatal day 1). Two groups were treated with MK-801 (1 or 2 mg/kg) 0.5 h before the lesion and 6 and 14 h after, while one group received saline injections. A fourth group received MK-801 injections, but did not have a freezing lesion. The volume of neocortical abnormality was determined for all three groups in rats killed after postnatal day 7. Treatment with the higher dose of MK-801 (3 x 2 mg/kg) dramatically reduced the effects of freezing injury but also resulted in over 50% mortality in both lesioned and unlesioned groups. Animals in the lesioned group, however, had a decreased volume of abnormal cortex, and there were fewer animals with microsulci than in the untreated group. This is the first demonstration of a significant anatomical neuroprotective effect in newborns leading to a reduction of cortical malformation.

摘要

四层微小脑回与许多发育障碍相关,包括智力迟钝、癫痫和发育性阅读障碍。对新生啮齿动物的新皮质进行冷冻损伤会导致四层微小脑回的形成。先前的研究表明,这种类型的损伤对发育中的皮质板起到缺氧/缺血事件的作用。当前的研究考察了非竞争性N-甲基-D-天冬氨酸受体拮抗剂地佐环平(MK-801)在保护新生大鼠皮质板免受冷冻损伤方面的有效性。三组大鼠在出生第一天(出生后第1天)接受皮质板冷冻损伤。两组在损伤前0.5小时以及损伤后6小时和14小时用MK-801(1或2mg/kg)进行治疗,而一组接受生理盐水注射。第四组接受MK-801注射,但没有冷冻损伤。在出生后第7天处死的大鼠中,对所有三组测定新皮质异常的体积。用较高剂量的MK-801(3×2mg/kg)治疗显著降低了冷冻损伤的影响,但也导致损伤组和未损伤组的死亡率超过50%。然而,损伤组动物的异常皮质体积减小,与未治疗组相比,有微沟的动物更少。这是首次证明在新生儿中存在显著的解剖学神经保护作用,可减少皮质畸形。

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