Literature DB >> 21813398

Rat performance on visual detection task modeled with divisive normalization and adaptive decision thresholds.

Philip Meier1, Pamela Reinagel.   

Abstract

Performance on any perceptual task depends on both the perceptual capacity and the decision strategy of the subject. We provide a model to fit both aspects and apply it to data from rats performing a detection task. When rats must detect a faint visual target, the presence of other nearby stimuli ("flankers") increases the difficulty of the task. In this study, we consider two specific factors. First, flankers could diminish the sensory response to the target via spatial contrast normalization in early visual processing. Second, rats may treat the sensory signal caused by the flankers as if it belonged to the target. We call this source confusion, which may be sensory, cognitive, or both. We account for contrast normalization and source confusion by fitting model parameters to the likelihood of the observed behavioral data. We test multiple combinations of target and flanker contrasts using a yes/no detection task. Contrast normalization was crucial to explain the rats' flanker-induced detection impairment. By adding a decision variable to the contrast normalization framework, our model provides a new tool to assess differences in visual or cognitive brain function between normal and abnormal rodents.

Entities:  

Mesh:

Year:  2011        PMID: 21813398     DOI: 10.1167/11.9.1

Source DB:  PubMed          Journal:  J Vis        ISSN: 1534-7362            Impact factor:   2.240


  16 in total

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Journal:  J Neurophysiol       Date:  2014-02-26       Impact factor: 2.714

2.  Visual cognition: rats compare shapes among the crowd.

Authors:  Alberto Cruz-Martín; Andrew D Huberman
Journal:  Curr Biol       Date:  2012-01-10       Impact factor: 10.834

Review 3.  Probing perceptual decisions in rodents.

Authors:  Matteo Carandini; Anne K Churchland
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4.  Temporal and spatial tuning of dorsal lateral geniculate nucleus neurons in unanesthetized rats.

Authors:  Balaji Sriram; Philip M Meier; Pamela Reinagel
Journal:  J Neurophysiol       Date:  2016-03-02       Impact factor: 2.714

5.  Concurrent electrophysiological recording and cognitive testing in a rodent touchscreen environment.

Authors:  Brian D Kangas; Ann M Iturra-Mena; Mykel A Robble; Oanh T Luc; David Potter; Stefanie Nickels; Jack Bergman; William A Carlezon; Diego A Pizzagalli
Journal:  Sci Rep       Date:  2021-06-03       Impact factor: 4.996

6.  Dorsal lateral geniculate substructure in the long-evans rat: a cholera toxin B subunit study.

Authors:  Claire B Discenza; Pamela Reinagel
Journal:  Front Neuroanat       Date:  2012-09-25       Impact factor: 3.856

Review 7.  Invariant visual object recognition and shape processing in rats.

Authors:  Davide Zoccolan
Journal:  Behav Brain Res       Date:  2015-01-02       Impact factor: 3.332

8.  Male long-Evans rats: An outbred model of marked hypothalamic-pituitary-adrenal hyperactivity.

Authors:  Maria Sanchís-Ollé; Laura Sánchez-Benito; Silvia Fuentes; Humberto Gagliano; Xavier Belda; Patricia Molina; Javier Carrasco; Roser Nadal; Antonio Armario
Journal:  Neurobiol Stress       Date:  2021-06-17

9.  Evidence that primary visual cortex is required for image, orientation, and motion discrimination by rats.

Authors:  Sarah K Petruno; Robert E Clark; Pamela Reinagel
Journal:  PLoS One       Date:  2013-02-18       Impact factor: 3.240

10.  Rats and humans differ in processing collinear visual features.

Authors:  Philip M Meier; Pamela Reinagel
Journal:  Front Neural Circuits       Date:  2013-12-13       Impact factor: 3.492

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