Visually cued fear conditioning test for memory impairment related to cortical function
Aim Fear conditioning tests are intended to elucidate a subject's ability to associate a conditioned stimulus with an aversive, unconditioned stimulus, such as footshock. Among these tests, a paradigm related to precise cortical functions would be increasingly important in drug screening for di...
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Veröffentlicht in: | Neuropsychopharmacology reports 2020-12, Vol.40 (4), p.371-375 |
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Sprache: | eng |
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Zusammenfassung: | Aim
Fear conditioning tests are intended to elucidate a subject's ability to associate a conditioned stimulus with an aversive, unconditioned stimulus, such as footshock. Among these tests, a paradigm related to precise cortical functions would be increasingly important in drug screening for disorders such as schizophrenia and dementia. Therefore, we established a new fear conditioning paradigm using a visual cue in mice. In addition, the validity of the test was evaluated using a genetically engineered mouse, heterozygous deficient in Mdga1 (Mdga1+/‐), which is related to schizophrenia.
Results
Mice were given footshocks associated with a visual cue of moving gratings at training in 25‐minute sessions. The mice showed the conditioned response of freezing behavior to the visual stimulus at testing 24 hours after the footshocks. In the test for validation, the Mdga1+/‐ deficient mice showed significantly less freezing than wild‐type mice.
Conclusion
The visually cued fear conditioning paradigm with moving gratings has been established, which is experimentally useful to evaluate animal cortical functions. The validity of the test was confirmed for Mdga1‐deficient mice with possible deficiency in cortical functions.
The visual stimulus of moving gratings could be distinguished from still gratings by mice, and moving gratings were related to footshock. The defect obtained here by low‐frequency grating in MDGA1 deficient mice might reflect that the coarse gratings are less detectable in visual perceptions of the schizophrenic brain. |
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ISSN: | 2574-173X 2574-173X |
DOI: | 10.1002/npr2.12146 |