Fujimori Sayumi, Yoneda Yukio
Laboratory of Molecular Pharmacology, Kanazawa University Graduate School of Natural Science and Technology, Kakuma-machi, Kanazawa 920-1192, Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 2004 Oct;24(5):265-71.
In the mammalian central nervous system (CNS), the inhibitory GABAergic system is composed of different signaling molecules such as glutamate decaroxylase, vesicular GABA transporters, GABA receptors, GABA transporters and GABA transaminase. A prevailing view is that the balance between excitatory signaling mediated by glutamate and inhibitory signaling mediated by GABA plays a pivotal role in mechanisms underlying the modulation and maintenance of a variety of neural functions. Therefore, abnormalities in a GABAergic signaling molecule would lead to a crisis of severe symptoms relevant to a number of neuropsychiatric disorders. These include epilepsy, depression, schizophrenia, stiff-person syndrome, drug addiction and so on. In this review article, we will summarize recent studies on the relationship between the malfunction of GABAergic signaling molecules and the etiology of these neuropsychiatric disorders. We will also refer to novel strategies on GABAergic signaling molecules other than GABA receptors for therapeutic usefulness in the future.
在哺乳动物的中枢神经系统(CNS)中,抑制性γ-氨基丁酸(GABA)能系统由不同的信号分子组成,如谷氨酸脱羧酶、囊泡GABA转运体、GABA受体、GABA转运体和GABA转氨酶。一种普遍的观点是,由谷氨酸介导的兴奋性信号和由GABA介导的抑制性信号之间的平衡在多种神经功能的调节和维持机制中起着关键作用。因此,GABA能信号分子的异常会导致与许多神经精神疾病相关的严重症状危机。这些疾病包括癫痫、抑郁症、精神分裂症、僵人综合征、药物成瘾等。在这篇综述文章中,我们将总结关于GABA能信号分子功能障碍与这些神经精神疾病病因之间关系的最新研究。我们还将提及除GABA受体之外的GABA能信号分子在未来治疗中的新策略。