TY - JOUR
T1 - Electroretinograms to checkerboard pattern reversal in cats
T2 - physiological characteristics and effect of retrograde degeneration of ganglion cells
AU - Tobimatsu, Shozo
AU - Celesia, Gastone G.
AU - Cone, Sandra
AU - Gujrati, Meena
N1 - Funding Information:
Key words: Pattern ERGs; Spatial frequency tuning; Retina; Ganglion cells; Electroretinograms; Optic nerve; Retrograde degenera-tion ganglion cells Pattern electroretinogram (P-ERG) has been successfully utilized in clinical studies to evaluate diseases of the macula and the optic nerve (Fiorentini et al. 1981; Dawson et al. 1982; Sherman 1982; Bobak et al. 1983; Celesia and Kaufman 1985; Kaufman and Celesia 1985; Celesia et al. 1986; Ryan and Arden 1988). However, the generator sources of P-ERG are still controversial (Maffei and Fiorentini 1981, 1982; Arden and Vaegan 1983; Korth 1983; Bagnoli et al. 1984; Baker and Hess 1984; Hess and Baker 1984; Hol- I This study was supported by a grant from the Veterans Administration.
PY - 1989/10
Y1 - 1989/10
N2 - Pattern electroretinograms (P-ERGs) evoked by alternating checks were studied in cats. Spatial frequency functions for transient and steady-state P-ERG waves showed a bimodal distribution with a preferred frequency at 0.6-0.75 c/deg and a second amplitude increase at frequencies lower than 0.5 c/deg. Decreasing the pattern luminance by 0.5 log units produced a shift of the spatial tuning curve toward lower spatial frequencies. No temporal tuning was noted in the temporal frequency functions. The bimodal distribution suggests that at spatial frequencies higher than 0.5 c/deg, the tuning reflects a 'contrast response' originating in cells with center surround organization. At spatial frequencies below 0.5 c/deg, the 'luminance response' becomes predominant and is generated in cells sensitive to mean luminance changes. Transient and steady-state P-ERGs to medium and high spatial frequencies were abolished by section of the optic nerve, while low spatial frequency stimuli at or below 0.3 c/deg continued to evoke P-ERGs at 1, 5 and 10 months after surgery. Quantitative whole amount retina microscopic examination confirmed the retrograde degeneration of the ganglion cells. It is concluded that both transient and steady-state P-ERGs to small and medium spatial frequencies checks are predominantly related to ganglion cell activity, while P-ERGs to low spatial frequencies reflect preganglionic cell activity.
AB - Pattern electroretinograms (P-ERGs) evoked by alternating checks were studied in cats. Spatial frequency functions for transient and steady-state P-ERG waves showed a bimodal distribution with a preferred frequency at 0.6-0.75 c/deg and a second amplitude increase at frequencies lower than 0.5 c/deg. Decreasing the pattern luminance by 0.5 log units produced a shift of the spatial tuning curve toward lower spatial frequencies. No temporal tuning was noted in the temporal frequency functions. The bimodal distribution suggests that at spatial frequencies higher than 0.5 c/deg, the tuning reflects a 'contrast response' originating in cells with center surround organization. At spatial frequencies below 0.5 c/deg, the 'luminance response' becomes predominant and is generated in cells sensitive to mean luminance changes. Transient and steady-state P-ERGs to medium and high spatial frequencies were abolished by section of the optic nerve, while low spatial frequency stimuli at or below 0.3 c/deg continued to evoke P-ERGs at 1, 5 and 10 months after surgery. Quantitative whole amount retina microscopic examination confirmed the retrograde degeneration of the ganglion cells. It is concluded that both transient and steady-state P-ERGs to small and medium spatial frequencies checks are predominantly related to ganglion cell activity, while P-ERGs to low spatial frequencies reflect preganglionic cell activity.
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U2 - 10.1016/0013-4694(89)90112-0
DO - 10.1016/0013-4694(89)90112-0
M3 - Article
C2 - 2477220
AN - SCOPUS:0024426995
SN - 0013-4694
VL - 73
SP - 341
EP - 352
JO - Electroencephalography and Clinical Neurophysiology
JF - Electroencephalography and Clinical Neurophysiology
IS - 4
ER -