In previous studies of saccadic eye movement reaction time, the manipulatio
n of initial eye position revealed a behavioral bias that facilitates the i
nitiation of movements towards the central orbital position. An interesting
hypothesis for this re-centering bias suggests that it reflects a visuo-mo
tor optimizing strategy, rather than peripheral muscular constraints. Given
that the range of positions that the eyes can take in the orbits delimits
the extent of visual exploration by head-fixed subjects, keeping the eyes c
entered in the orbits may indeed permit flexible orienting responses to eng
aging stimuli. To investigate the influence of initial eye position on cent
ral processes such as saccade selection and initiation, we examined the act
ivity of saccade-related neurons in the primate superior colliculus (SC). U
sing a simple reaction time paradigm wherein an initially fixated Visual st
imulus varying in position was extinguished 200 ms before the presentation
of a saccadic target, we studied the relationship between initial eye posit
ion and neuronal activation in advance of saccade initiation. We found that
the magnitude of the early activity of SC neurons, especially during the i
mmediate pre-target period that followed the fixation stimulus disappearanc
e, was correlated with changes in initial eye position. For the great major
ity of neurons, the pre-target activity increased with changes in initial e
ye position in the direction opposite to their movement fields, and it was
also strongly correlated with the concomitant reduction in reaction time of
centripetal saccades directed within their movement fields. Taking into ac
count the correlation with saccadic reaction time, the relationship between
neuronal activity and initial eye position remained significant. These res
ults suggest that eye-position-dependent changes in the excitability of SC
neurons could represent the neural substrate underlying a re-centering bias
in saccade regulation. More generally, the low frequency SC pre-target act
ivity could use eccentric eye position signals to regulate both when and wh
ich saccades are produced by promoting the emergence of a high frequency bu
rst of activity that can act as a saccadic command. However, only saccades
initiated within similar to 200 ms of target presentation were associated w
ith SC pre-target activity. This eye-dependent pre-target activation mechan
ism therefore appears to be restricted to the initiation of saccades with r
elatively short reaction times, which specifically require the integrity of
the SC.