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The Journal of Neurophysiology Vol. 84 No. 4 October 2000, pp. 1826-1834
Copyright ©2000 by the American Physiological Society
Department of Physiology, Keio University School of Medicine, Tokyo 160-8582, Japan
Watanabe, Shu-Ichi,
Amane Koizumi,
Shinya Matsunaga,
Jonathan W. Stocker, and
Akimichi Kaneko.
GABA-Mediated Inhibition Between Amacrine Cells in the
Goldfish Retina. J. Neurophysiol. 84: 1826-1834, 2000. Retinal amacrine cells have abundant dendro-dendritic
synapses between neighboring amacrine cells. Therefore an amacrine cell has both presynaptic and postsynaptic aspects. To understand these synaptic interactions in the amacrine cell, we recorded from amacrine cells in the goldfish retinal slice preparation with perforated- and
whole cell-patch clamp techniques. As the presynaptic element, 19% of
the cells recorded (15 of 78 cells) showed spontaneous tetrodotoxin
(TTX)-sensitive action potentials. As the postsynaptic element, all
amacrine cells (n = 9) were found to have GABA-evoked responses and, under perforated patch clamp, 50 µM GABA
hyperpolarized amacrine cells by activating a
Cl
conductance. Bicuculline-sensitive
spontaneous postsynaptic currents, carried by
Cl
, were observed in 82% of the cells (64 of
78 cells). Since the source of GABA in the inner plexiform layer is
amacrine cells alone, these events are likely to be inhibitory
postsynaptic currents (IPSCs) caused by GABA spontaneously released
from neighboring amacrine cells. IPSCs were classified into three
groups. Large amplitude IPSCs were suppressed by TTX (1 µM),
indicating that presynaptic action potentials triggered GABA release.
Medium amplitude IPSCs were also TTX sensitive. Small amplitude IPSCs
were TTX insensitive (miniature IPSCs; n = 26). All of
spike-induced, medium amplitude, and miniature IPSCs were
Ca2+ dependent and blocked by
Co2+. Blocking of glutamatergic inputs by
DL-2-amino-phosphonoheptanoate (AP7; 30 µM) and
6-cyano-7-nitroquinoxaline-2,3-dione (CNQX; 2 µM) had almost no
effect on spontaneous GABA release from presynaptic amacrine cells. We
suggest that these dendro-dendrotic inhibitory networks contribute to
receptive field spatiotemporal properties.
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