The eyecup preparation has traditionally been used to study retinal physiol
ogy in lower vertebrates and in some mammals. The procedures for preparing
eyecups of the rat and mouse have not been described, however. We now descr
ibe methods for preparing and maintaining viable eyecups for these two spec
ies. Eyecups were everted over a plastic dome and held in place between the
two halves of a superfusion chamber. Fluid exchange in the chamber was rap
id, with near total exchange occurring in 9 s. Eyecup viability was tested
by monitoring light-evoked retinal responses as the preparation aged. In bo
th rat and mouse, the amplitude of the electroretinogram (ERG) b-wave decre
ased slowly, declining to 1/2 maximal amplitude in approximate to 70 min. L
ight-evoked spike activity of neurons in the ganglion cell layer remained s
table for approximate to 3 h and attenuated responses were recorded for an
additional 1-2 h. Eyecups were able to dark adapt. Retinal sensitivity, tes
ted by monitoring b-wave amplitude, recovered following exposure to an adap
ting light. (C) 1999 Elsevier Science B.V. All rights reserved.