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兴奋性突触处神经递质转运体的变构调节。

Allosteric modulation of neurotransmitter transporters at excitatory synapses.

作者信息

Vandenberg Robert J, Ju Pengchu, Aubrey Karin R, Ryan Renae M, Mitrovic Ann D

机构信息

Department of Pharmacology, Institute for Biomedical Research, University of Sydney, Sydney 2006, NSW, Australia.

出版信息

Eur J Pharm Sci. 2004 Sep;23(1):1-11. doi: 10.1016/j.ejps.2004.05.006.

Abstract

The regulation of glutamate and glycine concentrations within excitatory synapses plays an important role in maintaining a dynamic signalling process between neurones, but the failure to regulate the concentrations of these neurotransmitters has been implicated in the pathogenesis of various neurological disorders. In this review we shall discuss how glutamate and glycine transporters regulate synaptic concentrations of these neurotransmitters and how endogenous allosteric modulators influence transporter function. Whilst glutamate transport inhibitors are unlikely to be of therapeutic value because their potential to cause excitoxicity and cell death, a greater understanding of how endogenous compounds allosterically modulate glutamate transporters may provide alternate drug targets. On the other hand, there are some promising drugs that inhibit glycine transporters, which are being trialled as an alternate treatment for schizophrenia. We shall discuss how the activity of one such compound may be expected to influence excitatory neurotransmission.

摘要

调节兴奋性突触内谷氨酸和甘氨酸的浓度在维持神经元之间动态信号传导过程中起着重要作用,但这些神经递质浓度调节失败与多种神经疾病的发病机制有关。在本综述中,我们将讨论谷氨酸和甘氨酸转运体如何调节这些神经递质的突触浓度,以及内源性变构调节剂如何影响转运体功能。虽然谷氨酸转运体抑制剂不太可能具有治疗价值,因为它们有导致兴奋毒性和细胞死亡的可能性,但更深入了解内源性化合物如何变构调节谷氨酸转运体可能会提供替代药物靶点。另一方面,有一些有前景的抑制甘氨酸转运体的药物正在作为精神分裂症的替代治疗方法进行试验。我们将讨论一种此类化合物的活性可能如何影响兴奋性神经传递。

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