Early-life exposure to noise reduces mPFC astrocyte numbers and T-maze alternation/discrimination task performance in adult male rats |
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Authors: | Yaveth Ruvalcaba-Delgadillo Sonia Luquín Rodrigo Ramos-Zú?iga Alfredo Feria-Velasco Rocío Elizabeth González-Casta?eda Maria Isabel Pérez-Vega Fernando Jáuregui-Huerta Joaquín García-Estrada |
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Institution: | Department of Neurosciences, University of Guadalajara, Guadalajara, Mexico;1.Department of Cellular and Molecular Biology, University of Guadalajara, Guadalajara, Mexico;2.Department of Earth and Life Sciences, University of Guadalajara, Guadalajara, Mexico;3.Department of Neurosciences, CIBO, Mexican Institute of Social Security, Guadalajara, Mexico |
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Abstract: | In this experiment, we evaluated the long-term effects of noise by assessing both astrocyte changes in medial prefrontal cortex (mPFC) and mPFC-related alternation/discrimination tasks. Twenty-one-day-old male rats were exposed during a period of 15 days to a standardized rats’ audiogram-fitted adaptation of a human noisy environment. We measured serum corticosterone (CORT) levels at the end of the exposure and periodically registered body weight gain. In order to evaluate the long-term effects of this exposure, we assessed the rats’ performance on the T-maze apparatus 3 months later. Astrocyte numbers and proliferative changes in mPFC were also evaluated at this stage. We found that environmental noise (EN) exposure significantly increased serum CORT levels and negatively affected the body weight gain curve. Accordingly, enduring effects of noise were demonstrated on mPFC. The ability to solve alternation/discrimination tasks was reduced, as well as the number of astroglial cells. We also found reduced cytogenesis among the mPFC areas evaluated. Our results support the idea that early exposure to environmental stressors may have long-lasting consequences affecting complex cognitive processes. These results also suggest that glial changes may become an important element behind the cognitive and morphological alterations accompanying the PFC changes seen in some stress-related pathologies. |
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Keywords: | Cingulate cortex cytogenesis development environmental stress glia working memory |
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