K. Funke et Ut. Eysel, INVERSE CORRELATION OF FIRING PATTERNS OF SINGLE TOPOGRAPHICALLY MATCHED PERIGENICULATE NEURONS AND CAT DORSAL LATERAL GENICULATE RELAY CELLS, Visual neuroscience, 15(4), 1998, pp. 711-729
Action potentials of single perigeniculate (PGN) cells and relay cells
of the dorsal lateral geniculate nucleus (dLGN) with topographically
matched or at least partially overlapping receptive fields (RF) were s
imultaneously recorded in the anesthetized and paralyzed cat during vi
sual stimulation with moving gratings or flashing light spots of diffe
rent size. In many cases, PGN cells showed an activity pattern which a
ppeared like a mirror image of distinct periods of dLGN activity. Flas
hing spots evoked transient volleys of activity in PGN cells which inc
reased in strength and shortened in latency with increasing size of th
e stimulus. These responses were temporally matched with inhibitory ph
ases in the early part of visual responses in the dLGN. The spatio-tem
poral properties of the RFs were established by reverse correlation of
the spike activity with the spatially random presentation of bright a
nd dark spots within an array of 20 x 20 positions. Anticorrelated fir
ing patterns of such kind could also be elicited as interocular inhibi
tion with stimulation of the perigeniculate RF in the nondominant eye.
Inversely correlated changes in spontaneous and visually induced acti
vity were also visible during spontaneous changes in EEG pattern. With
increasing synchronization of the EEG (predominance of delta-waves) t
he strength of geniculate visual responses declined while maintained p
erigeniculate activity increased. A weakened interocular and monocular
inhibition of dLGN relay cells during visual stimulation of PGN RFs c
ould be achieved with local reversible inactivation of PGN areas topog
raphically matched with the dLGN recording sites. The results indicate
that the PGN contributes to the state-dependent control of retino-gen
iculate transmission and to the monocular and interocular inhibitory p
rocesses that shape the visual responses in the dLGN.