If, as is widely believed, information is stored in the brain as distribute
d modifications of synaptic efficacy, it can be argued that the storage cap
acity of the brain will be maximized if the number of synapses that operate
independently is as large as possible. The majority of synapses in the bra
in are glutamatergic; their independence will be compromised if glutamate r
eleased at one synapse can significantly activate receptors at neighboring
synapses. There is currently no agreement on whether "spillover" after the
liberation of a vesicle will significantly activate receptors at neighborin
g synapses. To evaluate the independence of central synapses, it is necessa
ry to compare synaptic responses with those generated at neighboring synaps
es by glutamate spillover. Here, synaptic activation and spillover response
s are simulated in a model, based on data for hippocampal synapses, that in
cludes an approximate representation of the extrasynaptic space. Recently-p
ublished data on glutamate transporter distribution and properties are inco
rporated. Factors likely to influence synaptic or spillover responses are i
nvestigated. For release of one vesicle, it is estimated that the mean resp
onse at the nearest neighboring synapse will be <5% of the synaptic respons
e. It is concluded that synapses can operate independently.