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Fos imaging reveals differential neuronal activation of areas of rat temporal cortex by novel and familiar sounds Article (Published Version) http://sro.sussex.ac.uk Copyright and reuse:Sussex Research Online is a digital repository of the research output of the University.Copyright and all moral rights to the version of the paper presented here belong to the individual author(s) and/or other copyright owners. To the extent reasonable and practicable, the material made available in SRO has been checked for eligibility before being made available.Copies of full text items generally can be reproduced, displayed or performed and given to third parties in any format or medium for personal research or study, educational, or not-for-profit purposes without prior permission or charge, provided that the authors, title and full bibliographic details are credited, a hyperlink and/or URL is given for the original metadata page and the content is not changed in any way. AbstractTo provide information about the possible regions involved in auditory recognition memory, this study employed an imaging technique that has proved valuable in the study of visual recognition memory. The technique was used to image populations of neurons that are differentially activated by novel and familiar auditory stimuli, thereby paralleling previous studies of visual familiarity discrimination. Differences evoked by novel and familiar sounds in the activation of neurons were measured in different parts of the rat auditory pathway by immunohistochemistry for the protein product (Fos) of the immediate early gene c-fos. Signi®cantly higher counts of stained neuronal nuclei (266 6 21/mm 2 ) were evoked by novel than by familiar sounds (192 6 17/ mm 2 ) in the auditory association cortex (area Te3; AudA). No such signi®cant differences were found for the inferior colliculus, primary auditory cortex, postrhinal cortex, perirhinal cortex (PRH), entorhinal cortex, amygdala or hippocampus. These ®ndings are discussed in relation to the results of lesion studies and what is known of areas involved in familiarity discrimination for visual stimuli. Differential activation is produced by novel and familiar individual stimuli in sensory association cortex for both auditory and visual stimuli, whereas the PRH is differentially activated by visual but not auditory stimuli. It is suggested that this latter difference is related to the nature of the particular auditory and visual stimuli used.

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Thirteen dogs were trained to perform spatial delayed responses to auditory cues in a three-choice Nencki testing apparatus with a delay of 0 s and then 10 s with a criterion of 90% correct responses in 90 consecutive trials. Then six dogs received bilateral surgical removal of the hippocampus via the cortex of the suprasylvian gyrus (without additional injury to the entorhinal and parahippocampal cortex). Three dogs received control surgical ablation of the suprasylvian gyrus, which was damaged in ablation of the hippocampus, and four dogs served as intact controls. After the surgery or rest period, the dogs were tested for their retention (10-s delay), and then they were given additional tests with extended delays (30, 60, and 120 s) and with distractions during the 60-s delay period. In comparison with both control groups, dogs with hippocampal ablations had moderately impaired postoperative retention, as evidenced by the elevated numbers of errors on criterion. In subsequent stages of testing with extended delays, the impairment was greater and was significantly correlated with the extent of injury to the hippocampus. These data, together with an analysis of the animals' responses to the three-choice situation, indicate that in dogs lesions of the hippocampus impair spatial memory.