The electroretinogram (ERG) of the rhodopsin knockout (rho-/-) mouse of Hum
phries et al. (1997) (Humphries et al,, 1997) was studied for evidence of l
ight-evoked rod activity and to describe the cone function. The rho-/- reti
na develops normal numbers of rod and cone nuclei, but the rods have no out
er segments, and no rhodopsin is found by immunohistochemistry. The dark-ad
apted ERG threshold was elevated 4.7 log units above wild-type (WT) control
mice, indicating that any residual rod responses were reduced >50,000-fold
, consistent with a complete functional knockout. The dark-adapted rho-/- E
RG had a cone waveform, and the spectral sensitivity peaked near 510 nm for
both dark-adapted and light-adapted conditions, without evidence of a Purk
inje shift. The light-adapted ERG b-wave amplitude of young rho-/- mice was
the same as WT. The amplitude remained steady up to postnatal day P47, but
thereafter it declined to only 1-2% by P80 when no cone outer segments rem
ained. Cone b-wave threshold of dark-adapted rho-/- mice was -1.07 +/- 0.39
log cd-s/m(2) (n = 17), which is 1.27 log units more sensitive than light-
adapted thresholds against a rod-suppressing Ganzfeld background of 1.61 lo
g scotopic cd/m(2). This indicates that dark-adapted WT responses to still
dimmer stimuli are exclusively rod driven with minimal cone intrusion. Abov
e this cone threshold intensity, the dark-adapted b-wave of WT will be a su
mmation of rod and cone responses. Threshold versus intensity (TVI) studies
gave no evidence of a rod influence on the mouse cone b-wave.