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海马体CA1区锥体细胞上NMDA受体对镁离子敏感性的发育性增加。

Developmental increase in the sensitivity to magnesium of NMDA receptors on CA1 hippocampal pyramidal cells.

作者信息

Bowe M A, Nadler J V

机构信息

Department of Pharmacology, Duke University Medical Center, Durham, NC 27710.

出版信息

Brain Res Dev Brain Res. 1990 Oct 1;56(1):55-61. doi: 10.1016/0165-3806(90)90164-t.

Abstract

The N-methyl-D-aspartate (NMDA) receptor is involved in processes, such as associative learning, that are particularly important during early postnatal development. It has been suggested that the activity and regulation of this receptor changes during development. Activation of the NMDA receptor is normally limited by Mg2+ present in the extracellular fluid of brain. We have found that Mg2+ less potently antagonizes the depolarizing action of NMDA in developing rats than in adults. A grease-gap method was used to record depolarizations evoked in CA1 hippocampal pyramidal cells by the excitants NMDA and AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate). In the adult CA1 area, Mg2+ shifted the NMDA concentration-response curve to the right in a manner consistent with voltage-dependent open channel block (uncompetitive antagonism) in a preparation with significant receptor reserve. The potency of Mg2+ increased during development; a greater than two-fold change in the EC50 for Mg2+ was observed between 10-15 days of age and adulthood. A concentration of 10 mM reduced the maximum response of CA1 pyramidal cells to NMDA in adult rats, but not in developing rats. In addition, Mg2+ often enhanced the maximum depolarizations evoked by NMDA in 10- to 15-day-old rats, but very seldom in adults. No significant developmental changes in AMPA-induced depolarizations were observed in the presence or absence of Mg2+. These results suggest that synaptically released glutamate will readily activate NMDA receptors during early development and that its ability to do this declines with the maturation of the brain.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

N-甲基-D-天冬氨酸(NMDA)受体参与诸如联想学习等过程,这些过程在出生后早期发育阶段尤为重要。有人提出,该受体的活性和调节在发育过程中会发生变化。NMDA受体的激活通常受到存在于脑细胞外液中的Mg2+的限制。我们发现,与成年大鼠相比,Mg2+对发育中大鼠NMDA去极化作用的拮抗作用较弱。采用油脂间隙法记录兴奋性递质NMDA和AMPA(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸)诱发的海马CA1区锥体细胞的去极化。在成年CA1区,Mg2+使NMDA浓度-反应曲线右移,其方式与具有显著受体储备的制剂中的电压依赖性开放通道阻滞(非竞争性拮抗)一致。Mg2+的效力在发育过程中增加;在10至15日龄与成年期之间,观察到Mg2+的半数有效浓度(EC50)有超过两倍的变化。10 mM的浓度可降低成年大鼠CA1锥体细胞对NMDA的最大反应,但对发育中的大鼠则无此作用。此外,Mg2+常常增强10至15日龄大鼠中NMDA诱发的最大去极化,但在成年大鼠中则很少见。在有或没有Mg2+的情况下,均未观察到AMPA诱发的去极化有明显的发育变化。这些结果表明,在早期发育过程中,突触释放的谷氨酸将很容易激活NMDA受体,并且随着大脑的成熟,其激活NMDA受体的能力会下降。(摘要截短于250字)

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