1. Starburst amacrine cells were studied using whole cell patch record
ing. Displaced starburst cells were labeled in rabbit retinas by intra
ocular injection of 4,6-diamidino-2-phenylindole. The retinas were iso
lated and maintained in vitro. The inner limiting membrane and Muller
cell endfeet were removed mechanically from small areas above the star
burst cell bodies, allowing an unimpeded approach under visual control
to the cells. A total of 104 cells was studied.2. In voltage-clamp re
cordings, the cells responded to light with slow, graded inward and ou
tward currents on which were superimposed smaller, rapid inward curren
ts. The rapid inward currents appeared to be postsynaptic currents. 3.
The receptive fields of the cells were mapped using small spots. They
had an on-center, off-surround organization. Visualizing the dendrite
s by including Lucifer yellow in the patch pipette showed that the rec
eptive fields' centers closely approximated the dendritic spread of th
e neurons. 4. The cells' responses to movement were tested with smooth
movements or with two-spot apparent motion. No directional preference
was seen for spots swept across the whole receptive field, for centri
fugal movements, or for centripetal movements. 5. Bath-applied tetrodo
toxin (TTX) or intracellularly applied lidocaine N-ethyl bromide (QX-3
14) had no effect on any component of the spontaneous or light-evoked
activity. Depolarization of the cell bodies by injected current showed
evidence of active conductances, but they were unaffected by TTX or Q
X-314. 6. 6-Cyano-7-nitroquionxyline-2,3-dione eliminated the small ra
pid currents, indicating that they depend on lpha-amino-3-hydroxy-5-me
thyl-4-isoxazolepropionic acid/kainate glutamate receptors. 7. Because
it is unlikely that we voltage clamped the distalmost dendrites of th
ese wide-field cells, uncertainties remain about rapid electrical even
ts occurring in the dendrites. From a functional point of view, though
, the fact that slow responses to distal photic stimulation were recor
ded at the soma suggests that the starburst cells could in principle i
ntegrate inputs across fairly substantial fractions of their total den
dritic arbors. The extent to which this actually occurs remains to be
learned.