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Research Article | Open Access

Bidirectional modulation of unimodal object recognition by stressful and enriched experiences in mice

Department of Pathology of Sir Run Run Shaw Hospital and Department of Human Anatomy, Histology and Embryology, System Medicine Research Center, Center for Neuroscience, NHC and CAMS Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, China
Zhejiang University School of Medicine, Zhejiang University, Hangzhou 310058, China
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Abstract

Animals use cognitive behavior, by integrating information from multiple senses, to cope with the complex and changing environment. However, it is not yet understood how single sensory cognitive processes get modified and combined by multisensory cognition in these environments. To address this question, we exposed mouse to positive (tactile experience enrichment (TEE)) and negative (chronic restraint stress (CRS)) environments, and then studied how the dependence of their behavior on unimodal sensory (tactile or visual) processing was influenced by different environments. We found that TEE promoted object recognition behavior that depended on vision or tactile participation alone, whereas CRS impaired this dependence of behavior on single sensory channels. These results suggest that a positive environment promotes unimodal cognitive behavior, while the behavioral effect of negative environments is the opposite.

Keywords

visiontactileunimodal cognitiontactile experience enrichment (TEE)chronic restraint stress (CRS)

References

[1]

Stein, B. E., Stanford, T. R. Multisensory integration: Current issues from the perspective of the single neuron. Nature Reviews Neuroscience, 2008, 9(4): 255–266.
Crossref Google Scholar
[2]

Kim, J. J., Diamond, D. M. The stressed hippocampus, synaptic plasticity and lost memories. Nature Reviews Neuroscience, 2002, 3(6): 453–462.
Crossref Google Scholar
[3]

Sandi, C., Pinelo-Nava, M. T. Stress and memory: Behavioral effects and neurobiological mechanisms. Neural Plasticity, 2007, 2007: 78970.
Crossref Google Scholar
[4]

Santomauro, D. F., Herrera, A.M.M., Shadid, J., Zheng, P., Ashbaugh, C., Pigott, D. M., Abbafati, C., Adolph, C., Amlag, J. O., Aravkin, A. Y. et al. Global prevalence and burden of depressive and anxiety disorders in 204 countries and territories in 2020 due to the COVID-19 pandemic. Lancet, 2021, 398(10312): 1700–1712.
Crossref Google Scholar
[5]

Cloke, J. M., Jacklin, D. L., Winters, B. D. The neural bases of crossmodal object recognition in non-human Primates and rodents: A review. Behavioural Brain Research, 2015, 285: 118–130.
Crossref Google Scholar
[6]

Wang, C., Liu, H., Li, K., Wu, Z. Z., Wu, C., Yu, J. Y., Gong, Q., Fang, P., Wang, X. X., Duan, S. M. et al. Tactile modulation of memory and anxiety requires dentate granule cells along the dorsoventral axis. Nature Communications, 2020, 11(1): 6045.
Crossref Google Scholar
[7]

Whiteford, H. A., Degenhardt, L., Rehm, J., Baxter, A. J., Ferrari, A. J., Erskine, H. E., Charlson, F. J., Norman, R. E., Flaxman, A. D., Johns, N. et al. Global burden of disease attributable to mental and substance use disorders: Findings from the Global Burden of Disease Study 2010. Lancet, 2013, 382(9904): 1575–1586.
Crossref Google Scholar
[8]

Wang, X. D., Su, Y. A., Wagner, K. V., Avrabos, C., Scharf, S. H., Hartmann, J., Wolf, M., Liebl, C., Kühne, C., Wurst, W. et al. Nectin-3 links CRHR1 signaling to stress-induced memory deficits and spine loss. Nature Neuroscience, 2013, 16(6): 706–713.
Crossref Google Scholar
[9]

Wang, X. X., Li, J. T., Xie, X. M., Gu, Y., Si, T. M., Schmidt, M. V., Wang, X. D. Nectin-3 modulates the structural plasticity of dentate granule cells and long-term memory. Translational Psychiatry, 2017, 7(9): e1228.
Crossref Google Scholar
[10]

Mao, M. J., Gao, Y. Z., Yang, J. J., Zhou, Z. Q., Ji, M. H. Abnormal theta oscillation aggravated by chronic stress in the CA1 may mediate the deterioration of fear memory impairment induced by lipopolysaccharide. Brain Research Bulletin, 2021, 171: 172–182.
Crossref Google Scholar
[11]

Notaras, M., van den Buuse, M. Neurobiology of BDNF in fear memory, sensitivity to stress, and stress-related disorders. Molecular Psychiatry, 2020, 25(10): 2251–2274.
Crossref Google Scholar
[12]

Wang, H. L., Li, J. T., Wang, H., Sun, Y. X., Liu, R., Wang, X. D., Su, Y. N., Si, T. M. Prefrontal Nectin3 reduction mediates adolescent stress-induced deficits of social memory, spatial working memory, and dendritic structure in mice. Neuroscience Bulletin, 2020, 36(8): 860–874.
Crossref Google Scholar
[13]

Ciaramelli, E., Moscovitch, M. The space for memory in posterior parietal cortex: re-analyses of bottom-up attention data. Neuropsychologia, 2020, 146: 107551.
Crossref Google Scholar
[14]

Zhang, C. Y., Aflalo, T., Revechkis, B., Rosario, E. R., Ouellette, D., Pouratian, N., Andersen, R. A. Partially mixed selectivity in human posterior parietal association cortex. Neuron, 2017, 95(3): 697–708.e4.
Crossref Google Scholar
[15]

Parvizi, J., Wagner, A. D. Memory, numbers, and action decision in human posterior parietal cortex. Neuron, 2018, 97(1): 7–10.
Crossref Google Scholar
[16]

Meijer, G. T., Mertens, P. E. C., Pennartz, C. M. A., Olcese, U., Lansink, C. S. The circuit architecture of cortical multisensory processing: Distinct functions jointly operating within a common anatomical network. Progress in Neurobiology, 2019, 174: 1–15.
Crossref Google Scholar
[17]

Chen, H., Uddin, L. Q., Zhang, Y. X., Duan, X. J., Chen, H. F. Atypical effective connectivity of thalamo-cortical circuits in autism spectrum disorder. Autism Research: Official Journal of the International Society for Autism Research, 2016, 9(11): 1183–1190.
Crossref Google Scholar
[18]

Libovner, Y., Fariborzi, M., Tabba, D., Ozgur, A., Jafar, T., Lur, G. Repeated exposure to multiple concurrent stresses induce circuit specific loss of inputs to the posterior parietal cortex. The Journal of Neuroscience, 2020, 40(9): 1849–1861
Crossref Google Scholar
[19]

Hindley, E. L., Nelson, A. J. D., Aggleton, J. P., Vann, S. D. Dysgranular retrosplenial cortex lesions in rats disrupt cross-modal object recognition. Learning & Memory, 2014, 21(3): 171–179.
Crossref Google Scholar
Stress and Brain
Volume 3 Issue 1,
March 2023
Pages 35-46
DOI: 10.26599/SAB.2022.9060032
Cite this article:
Wang C, Xu L-T, Chen Y-F, et al. Bidirectional modulation of unimodal object recognition by stressful and enriched experiences in mice. Stress and Brain, 2023, 3(1): 35-46. https://doi.org/10.26599/SAB.2022.9060032

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Received: 14 October 2022
Revised: 24 February 2023
Accepted: 03 April 2023
Published: 04 May 2023
© The Author(s) 2023

Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attributtion-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission.
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