Dynamic action of neurometals at the synapse

被引:57
作者
Tamano, Haruna [1 ]
Takeda, Atsushi [1 ]
机构
[1] Univ Shizuoka, Global COE, Sch Pharmaceut Sci, Dept Med Biochem,Suruga Ku, Shizuoka 4228526, Japan
关键词
LONG-TERM POTENTIATION; BLOOD-BRAIN-BARRIER; LOW MICROMOLAR CONCENTRATIONS; HIPPOCAMPAL CA1 SYNAPSES; CENTRAL-NERVOUS-SYSTEM; NMDA RECEPTOR-CHANNEL; MOSSY FIBER CALCIUM; CEREBROSPINAL-FLUID; ZINC INHIBITION; NEURONAL EXCITABILITY;
D O I
10.1039/c1mt00008j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are synaptic vesicles that are labeled by Timm's sulfide-silver staining method in the brain, suggesting that synaptic vesicles contain metals such as zinc and copper. Zinc is co-released with glutamate and the importance of zinc signaling in the intracellular compartment, in addition to extracellular compartment, is becoming recognized. Zinc can pass through calcium channels, while blocking them. Calcium signaling plays a critical role for synaptic activity and crosstalk between zinc signaling with calcium signaling through calcium channels may participate in synaptic neurotransmission including synaptic plasticity such as long-term potentiation. Copper released into the synaptic cleft during synaptic excitation may also participate in synaptic neurotransmission. Other metals including copper potentially serve as calcium channel blockers and also influence calcium signaling and zinc signaling via the interaction with metal-binding proteins such as metallothioneins. Homeostasis of metals needs to be controlled spatiotemporally for proper brain function, and their dyshomeostasis is associated with neurological diseases. However, the data on the dynamic action of metals at synapses is limited and their significance poorly understood. This paper summarizes the action of metals in synaptic neurotransmission focused on calcium signaling at glutamatergic synapses.
引用
收藏
页码:656 / 661
页数:6
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