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大鼠嗅球中N-甲基-D-天冬氨酸受体对细胞死亡的调节

NMDA receptor regulation of cell death in the rat olfactory bulb.

作者信息

Fiske B K, Brunjes P C

机构信息

Neuroscience Program, University of Virginia, Charlottesville, Virginia 22903, USA.

出版信息

J Neurobiol. 2001 Jun 5;47(3):223-32. doi: 10.1002/neu.1029.

DOI:10.1002/neu.1029
PMID:11333403
Abstract

Cell death is widespread in the developing nervous system and is under complex regulation by numerous intra- and intercellular mechanisms. Blockade of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptor has been shown to promote cell death in the developing brain (Ikonomidou et al., 1999), suggesting that afferent functional activation is an important regulator of cell survival. The olfactory bulb, the first central relay for olfactory information from the nose, is well suited for examining the role of afferent activity in neuronal development. Functional deprivation is easily performed by surgical blockade of airflow to one side of the nasal passage, which results in dramatic alterations in postnatal development of the bulb (Brunjes, 1994), including enhanced neuronal loss (Frazier and Brunjes, 1988; Najbauer and Leon, 1995). The present report examined the specific role of NMDA receptor activation in regulating cell survival within the rat bulb. Pharmacological blockade of receptors with the noncompetitive channel blocker MK-801 (3 x 0.5 mg/kg i.p.) resulted in profound increases in cell death within 24 h. Furthermore, in contrast to other regions, where the effects of receptor blockade were confined to the first 2 postnatal weeks (Ikonomidou et al., 1999), enhancement of cell death was seen in the deeper granule cell-containing regions of the bulb with injections as late as postnatal day 28. In addition, the effects of MK-801 were much more dramatic than those seen after unilateral naris closure, suggesting that NMDA receptor activation may mediate additional survival pathways in the bulb beyond that provided by first nerve input.

摘要

细胞死亡在发育中的神经系统中广泛存在,并受到众多细胞内和细胞间机制的复杂调控。已表明,阻断谷氨酸受体的N-甲基-D-天冬氨酸(NMDA)亚型可促进发育中大脑的细胞死亡(伊科诺米杜等人,1999年),这表明传入功能激活是细胞存活的重要调节因子。嗅球是来自鼻子的嗅觉信息的第一个中枢中继站,非常适合用于研究传入活动在神经元发育中的作用。通过手术阻断一侧鼻道的气流很容易实现功能剥夺,这会导致嗅球出生后发育的显著改变(布伦耶斯,1994年),包括神经元损失增加(弗雷泽和布伦耶斯,1988年;纳伊鲍尔和利昂,1995年)。本报告研究了NMDA受体激活在调节大鼠嗅球内细胞存活中的具体作用。用非竞争性通道阻滞剂MK-801(3×0.5毫克/千克腹腔注射)进行受体的药理学阻断,导致24小时内细胞死亡显著增加。此外,与其他区域不同,在其他区域受体阻断的影响仅限于出生后的前两周(伊科诺米杜等人,1999年),在出生后第28天注射时,在嗅球含有更深层颗粒细胞的区域仍可见细胞死亡增加。此外,MK-801的作用比单侧鼻孔关闭后的作用要显著得多,这表明NMDA受体激活可能介导嗅球中除第一神经输入所提供的生存途径之外的其他生存途径。

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