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通过乳腺造影术评估发现,轻度应激通过N-甲基-D-天冬氨酸受体短暂刺激大鼠海马体的葡萄糖利用。

Mild stress stimulates rat hippocampal glucose utilization transiently via NMDA receptors, as assessed by lactography.

作者信息

Schasfoort E M, De Bruin L A, Korf J

机构信息

Department of Biological Psychiatry, Psychiatric University Clinic, Groningen, The Netherlands.

出版信息

Brain Res. 1988 Dec 13;475(1):58-63. doi: 10.1016/0006-8993(88)90198-9.

DOI:10.1016/0006-8993(88)90198-9
PMID:2850837
Abstract

Lactography is a novel technique that allows the continuous on-line registration of brain extracellular lactate in the freely behaving animal and that is based on a fluorimetric enzymatic assay of brain dialysates. Electroconvulsive shock, activation of the glutamate receptor (NMDA-type) and mild stress (immobilization, cold stress or handling) result in transient increases in the efflux of lactate from the rat hippocampus. The increase following immobilization stress was attenuated by the NMDA-receptor antagonist 2-amino-5-phosphopentanoic acid and after several pre-exposures to this stressor. These experiments suggest that mild stress activates glutamatergic neurons, which may be less after habituation to stress.

摘要

乳腺造影术是一种新颖的技术,它能够在自由活动的动物体内连续在线记录脑细胞外乳酸水平,且该技术基于对脑透析液的荧光酶测定法。电休克、谷氨酸受体(NMDA型)激活以及轻度应激(固定、冷应激或处理)会导致大鼠海马体乳酸外流短暂增加。固定应激后的增加被NMDA受体拮抗剂2-氨基-5-磷酸戊酸减弱,并且在多次预先暴露于该应激源后也会减弱。这些实验表明,轻度应激会激活谷氨酸能神经元,而在适应应激后这种激活可能会减少。

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1
Mild stress stimulates rat hippocampal glucose utilization transiently via NMDA receptors, as assessed by lactography.通过乳腺造影术评估发现,轻度应激通过N-甲基-D-天冬氨酸受体短暂刺激大鼠海马体的葡萄糖利用。
Brain Res. 1988 Dec 13;475(1):58-63. doi: 10.1016/0006-8993(88)90198-9.
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Rat hippocampal lactate efflux during electroconvulsive shock or stress is differently dependent on entorhinal cortex and adrenal integrity.在电惊厥休克或应激期间,大鼠海马乳酸外流对内嗅皮层和肾上腺完整性的依赖程度不同。
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Physiological stimulation increases nonoxidative glucose metabolism in the brain of the freely moving rat.生理刺激会增加自由活动大鼠大脑中的非氧化葡萄糖代谢。
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CGP 37849 and CGP 39551: novel and potent competitive N-methyl-D-aspartate receptor antagonists with oral activity.CGP 37849和CGP 39551:新型强效竞争性N-甲基-D-天冬氨酸受体拮抗剂,具有口服活性。
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