Zmj. Zhou et al., AMINO-ACID RECEPTORS OF MIDGET AND PARASOL GANGLION-CELLS IN PRIMATE RETINA, Proceedings of the National Academy of Sciences of the United Statesof America, 91(11), 1994, pp. 4907-4911
Primate retinas contain two major ganglion cell types. Midget (or P ty
pe) cells have relatively sustained responses to light; the amplitude
and polarity of these responses vary with stimulus wavelength. Parasol
(or M type) cells are more sensitive to stimulus contrast and respond
more transiently but are not selective for color. Both types can be f
urther subdivided into a and b subtypes, according to the level of the
ir dendritic stratification in the inner plexiform layer. To determine
whether differences in receptors for amino acid transmitters are the
basis for any differences in ganglion cell light responses, we made wh
ole-cell, patch-clamp recordings from identified ganglion cells in sli
ce preparations of macaque and baboon retinas. We found that midget an
d parasol cells of both a and b types had similar responses to excitat
ory amino acids, including kainate, pha-amino-3-hydroxy-5-methylisoxal
zole-4-propionic acid, and N-methyl-D-aspartate, with reversal potenti
als near the equilibrium potential for cations. Kainate responses were
blocked by 6,7-dinitroquinoxaline, and N-methyl-D-aspartate responses
were blocked by D-(-)-2-amino-7-phosphonoheptanoic acid. The four typ
es of ganglion cells also had similar responses to bath-applied inhibi
tory amino acids. All cells had both gamma-aminobutyric acid and glyci
ne receptors with reversal potentials near the equilibrium potential f
or Cl-, and the relative amplitudes of the responses to excitatory and
inhibitory amino acids were similar among the various cell types. The
se results suggest that the differences in response properties of the
different classes of ganglion cells in primate retina may be determine
d, to a significant degree, by the properties of the amacrine and bipo
lar cells that provide their input rather than by the nature of their
postsynaptic receptors.