Li Yang V, Hough Christopher J, Sarvey John M
Department of Pharmacology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.
Sci STKE. 2003 May 13;2003(182):pe19. doi: 10.1126/stke.2003.182.pe19.
Chelatable Zn(2+), which is found in the synaptic vesicles of certain glutamatergic neurons in several regions of the forebrain, is released during neuronal activity. Zn(2+) exhibits numerous effects on ligand-gated and voltage-dependent ion channels, and released Zn(2+) is therefore likely able to modulate synaptic transmission. The physiologically relevant actions of Zn(2+), however, have remained unclear. Recent research exploiting improved Zn(2+)-sensitive optical probes has suggested some intriguing effects for synaptically released Zn(2+), including heterosynaptic regulation of N-methyl-D-aspartate (NMDA) receptor function, and a novel role as a trans-synaptic second messenger that may enter postsynaptic neurons to modulate various signal transduction pathways.
可螯合的锌离子(Zn(2+))存在于前脑多个区域某些谷氨酸能神经元的突触小泡中,在神经元活动时释放。Zn(2+) 对配体门控离子通道和电压依赖性离子通道有多种作用,因此释放的 Zn(2+) 很可能能够调节突触传递。然而,Zn(2+) 的生理相关作用仍不清楚。最近利用改进的 Zn(2+) 敏感光学探针进行的研究表明,突触释放的 Zn(2+) 有一些有趣的作用,包括对 N-甲基-D-天冬氨酸(NMDA)受体功能的异突触调节,以及作为一种可能进入突触后神经元以调节各种信号转导途径的跨突触第二信使的新作用。