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高苯丙氨酸血症导致HPH-5小鼠大脑中神经递质受体丧失。

Loss of neurotransmitter receptors by hyperphenylalaninemia in the HPH-5 mouse brain.

作者信息

Hommes F A

机构信息

Department of Pediatrics, New York University Medical Center, NY 10016, USA.

出版信息

Acta Paediatr Suppl. 1994 Dec;407:120-1. doi: 10.1111/j.1651-2227.1994.tb13469.x.

Abstract

The binding of the muscarinic acetylcholine antagonist quinuclinidylbensilate to its specific receptors was measured by quantitative autoradiography in the brain of the HPH-5 mouse, a phenylalanine hydroxylase-deficient mouse mutant, as a model for human PKU. Three types of response to a hyperphenylalaninemic condition were observed: no effect as in the putamen; a gradual decrease over time such as in several areas of the cerebral cortex and the hippocampus; a transient increase, followed by a decrease, such as in the frontal area of the cerebral cortex. Of particular significance is the effect on the CA1 and CA3 layer of the hippocampus, since this structure has been implicated in the acquisition and storage of long-term memory. Hyperphenylalaninemia leads to a decrease in neurotransmitter receptor density and, therefore, to a decrease in connectivity, which may form the basis for the mental retardation in this condition.

摘要

以苯丙氨酸羟化酶缺陷型小鼠突变体HPH - 5小鼠的大脑作为人类苯丙酮尿症(PKU)的模型,通过定量放射自显影法测定了毒蕈碱型乙酰胆碱拮抗剂喹核醇基苯酸盐与其特异性受体的结合情况。观察到对高苯丙氨酸血症状态有三种类型的反应:如在壳核中无影响;如在大脑皮层和海马体的几个区域随时间逐渐减少;短暂增加后又减少,如在大脑皮层额叶区域。对海马体CA1和CA3层的影响尤为重要,因为该结构与长期记忆的获取和存储有关。高苯丙氨酸血症导致神经递质受体密度降低,进而导致连接性降低,这可能是这种情况下智力发育迟缓的基础。

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