<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park SB</submitter><funding>NIDCD NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>100660</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11296072</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31</volume><pubmed_abstract>Chronic stress is well known to erode cognitive functions. Yet, our understanding of how repeated stress exposure impacts one of the fundamental bases of cognition: sensory processing, remains limited. The posterior parietal cortex (PPC) is a high order visual region, known for its role in visually guided decision making, multimodal integration, attention, and working memory. Here, we used functional measures to determine how repeated exposure to multiple concurrent stressors (RMS) affects sensory processing in the PPC in adult male mice. A longitudinal experimental design, repeatedly surveying the same population of neurons using &lt;i>in vivo&lt;/i> two-photon imaging, revealed that RMS disrupts the balanced turnover of visually responsive cells in layer 2/3 of the PPC. Across the population, RMS-induced changes in visual responsiveness followed a bimodal distribution suggesting idiosyncratic stress effects. In cells that maintained their responsiveness across recording sessions, we found that stress reduced visual response magnitudes and feature selectivity. While we did not observe stress-induced elimination of excitatory synapses, noise correlation statistics indicated that RMS altered visual input to the neuronal population. The impact of RMS was restricted to visually evoked responses and was not evident in neuronal activity associated with locomotion onset. Together, our results indicate that despite no apparent synaptic reorganization, stress exposure in adulthood can disrupt sensory processing in the PPC, with the effects showing remarkable individual variation.</pubmed_abstract><journal>Neurobiology of stress</journal><pubmed_title>Repeated exposure to multiple concurrent stressors alters visual processing in the adult posterior parietal cortex.</pubmed_title><pmcid>PMC11296072</pmcid><funding_grant_id>T32 DC010775</funding_grant_id><funding_grant_id>P30 CA062203</funding_grant_id><funding_grant_id>P50 GM076516</funding_grant_id><funding_grant_id>R01 MH123686</funding_grant_id><pubmed_authors>Park SB</pubmed_authors><pubmed_authors>Lur G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Repeated exposure to multiple concurrent stressors alters visual processing in the adult posterior parietal cortex.</name><description>Chronic stress is well known to erode cognitive functions. Yet, our understanding of how repeated stress exposure impacts one of the fundamental bases of cognition: sensory processing, remains limited. The posterior parietal cortex (PPC) is a high order visual region, known for its role in visually guided decision making, multimodal integration, attention, and working memory. Here, we used functional measures to determine how repeated exposure to multiple concurrent stressors (RMS) affects sensory processing in the PPC in adult male mice. A longitudinal experimental design, repeatedly surveying the same population of neurons using &lt;i>in vivo&lt;/i> two-photon imaging, revealed that RMS disrupts the balanced turnover of visually responsive cells in layer 2/3 of the PPC. Across the population, RMS-induced changes in visual responsiveness followed a bimodal distribution suggesting idiosyncratic stress effects. In cells that maintained their responsiveness across recording sessions, we found that stress reduced visual response magnitudes and feature selectivity. While we did not observe stress-induced elimination of excitatory synapses, noise correlation statistics indicated that RMS altered visual input to the neuronal population. The impact of RMS was restricted to visually evoked responses and was not evident in neuronal activity associated with locomotion onset. Together, our results indicate that despite no apparent synaptic reorganization, stress exposure in adulthood can disrupt sensory processing in the PPC, with the effects showing remarkable individual variation.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-05T06:26:16.99Z</modification><creation>2025-02-19T02:27:05.954Z</creation></dates><accession>S-EPMC11296072</accession><cross_references><pubmed>39100726</pubmed><doi>10.1016/j.ynstr.2024.100660</doi></cross_references></HashMap>