Sustained potential shifts, alterations in acoustic evoked potential amplitude and bradycardiac responses to the onset of illumination in the goldfish (Carassius auratus)

Abstract

Sustained potential shift's (SPSs) and changes in acoustic evoked potential (AEP) amplitudes were recorded from medullary and mid-brain regions in restrained goldfish (Carassius auratus) in response to the onset of illumination against a sensory background restricted to repetitive (1/s) acoustic stimulation. At the tectal surface, a long duration negative SPS, significant 5–10 s after the onset of illumination, was recorded with a maximum negativity of ca. 145 μV. Changes in acoustic responsiveness were also most apparent in the mid-brain where attenuations in AEP amplitude of ca. 15% were recorded. In general, AEPs exhibited attenuated amplitudes in response to the onset of illumination, perhaps reflecting attentional rather than arousal processes, arousal generally being associated with heightened sensory responsiveness. Changes in the amplitude of the medullary AEPs were directly related to the magnitude of bradycardiac responses such that lesser attenuations of the medullary AEP were associated with greater magnitude bradycardiac responses, suggesting a possible interaction of attentional and arousal processes. In response to repeated onset of illumination, SPSs tended towards increasing positivity (increasing in positivity at the medullary surface; decreasing in negativity at the tectal surface). The attenuation of AEPs recorded from the medulla and mid-brain habituated in response to stimulus repetition. Changes in amplitude of AEPs (ΔAEP) recorded from the telencephalon and the torus semicircularis region of the mid-brain were correlated with locally recorded SPSs. At the telencephalon, this correlation was inverse; enhanced AEP amplitudes being associated with SPS negativity, attenuated AEP amplitudes with SPS positivity. In the torus semicircularis, experiential changes in SPS and ΔAEP were directly correlated. As the SPS is considered to reflect glial redistribution of [K+]e (Roitbak 1983), glia may contribute to changes in measures of sensory responsivity, such as the AEP, during changes in behavioural state.