Frederickson C J, Moncrieff D W
Laboratory for Neurobiology, University of Texas at Dallas, Richardson 75083.
Biol Signals. 1994 May-Jun;3(3):127-39. doi: 10.1159/000109536.
Zinc-containing neurons are cells that sequester zinc in their presynaptic vesicles and release it in a calcium- and impulse-dependent manner. The zinc-containing neurons are a subclass of the glutaminergic neurons: all known zinc-containing pathways are also glutaminergic pathways. With a few exceptions, zinc-containing neurons are located only in the telencephalon. The major glutaminergic systems of the brain stem, thalamus, and cerebellum, for example, all lack vesicular zinc, whereas many cerebrocortical systems are zinc containing. Within the telencephalon, the zinc-containing fiber systems form a vast associational network that reciprocally interconnects isocortical, allocortical and 'limbic' structures. Because the hippocampal, amygdalar, and perirhinal regions are prominent nodes in this network, it is presumed that vesicular zinc is involved in epileptic phenomena (in pathology) and (in normal function) in the synaptic plasticity of developmental and experiential learning. Zinc ions are potent modulators of amino acid receptors [especially the N-methyl-D-aspartate (NMDA) receptor] and corelease of zinc along with glutamate would provide a mechanism for modulating postsynaptic excitability levels. One useful hypothesis is that synaptically released zinc controls a 'window' of postsynaptic excitability, having little or no effect at physiological firing rates, but selectively depressing excitability (by NMDA receptor depression) when firing rates reach dangerous, paroxysmal levels.
含锌神经元是一类在突触前囊泡中储存锌并以钙和冲动依赖方式释放锌的细胞。含锌神经元是谷氨酸能神经元的一个亚类:所有已知的含锌通路也是谷氨酸能通路。除了少数例外,含锌神经元仅位于端脑。例如,脑干、丘脑和小脑的主要谷氨酸能系统都缺乏囊泡锌,而许多大脑皮质系统则含有锌。在端脑内,含锌纤维系统形成一个庞大的联合网络,该网络将同型皮质、异质皮质和“边缘”结构相互连接。由于海马体、杏仁核和嗅周区域是这个网络中的重要节点,因此推测囊泡锌在癫痫现象(病理学上)以及发育性和经验性学习的突触可塑性(正常功能中)中发挥作用。锌离子是氨基酸受体(尤其是N-甲基-D-天冬氨酸(NMDA)受体)的强效调节剂,锌与谷氨酸的共同释放将提供一种调节突触后兴奋性水平的机制。一个有用的假说是,突触释放的锌控制着突触后兴奋性的“窗口”,在生理放电频率下几乎没有影响,但当放电频率达到危险的阵发性水平时,会通过抑制NMDA受体选择性地降低兴奋性。