The retina is the most accessible piece of central gray matter in the
vertebrate brain. Its wide dynamic operational range makes it the idea
l neuronal network to study its excitability. Spreading depression wav
es in the retina are accompanied by strong intrinsic optical signals (
IOS) and thus can be measured non-invasively with optical methods. Add
itionally, incubation with fluorescent dyes allows to follow calcium f
luxes in parallel. The IOS can be divided into red and green scatter o
f light. We show that during spreading depression the red scatter sign
al precedes the green scatter signal and that the calcium signal match
es the red scatter signal. Incubation of the retina with barium chlori
de leads to a reversible depression of red scatter and calcium signal
whereas the green scatter signal is hardly effected. The wave propagat
ion velocity is reduced, too. This supports the idea that the early re
d scatter signal is a direct visualisation of glial membrane potential
and that glia cells in the chicken retina are involved in the control
of extracellular calcium.