Much less attention has been paid to Zn in artificial cerebrospinal fluid (ACSF), i.e., extracellular medium, used for in vitro slice experiments than divalent cations such as Ca. Approximately 2 mM Ca is added to conventional ACSF from essentiality of Ca signaling in neurons and glial cells. However, no Zn is added to it, even though the importance of Zn signaling in them is recognizing. On the other hand, synaptic Zn homeostasis is changed during brain slice preparation. Therefore, it is possible that not only neuronal excitation but also synaptic plasticity such as long-term potentiation is modified in ACSF without Zn, in which original physiology might not appear. The basal (static) levels of intracellular (cytosolic) Zn and Ca are not significantly different between brain slices prepared with conventional ACSF without Zn and pretreated with ACSF containing 20 nM ZnCl for 1 h. In the case of mossy fiber excitation, however, presynaptic activity assessed with FM 4-64 is significantly suppressed in the stratum lucidum of brain slices pretreated with ACSF containing Zn, indicating that hippocampal excitability is enhanced in brain slices prepared with ACSF without Zn. The evidence suggests that low nanomolar concentration of Zn is necessary for ACSF. Furthermore, exogenous Zn has opposite effect on LTP induction between in vitro and in vivo experiments. It is required to pay attention to extracellular Zn concentration to understand synaptic function precisely.