Microglial and astroglial reaction in the olfactory bulb of mice after Triton X-100 application |
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Authors: | Jeongtae Kim Yuna Choi Meejung Ahn Poornima Ekanayake Akane Tanaka Hiroshi Matsuda Taekyun Shin |
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Affiliation: | 1. Department of Veterinary Anatomy, College of Veterinary Medicine and Veterinary Medical Research Institute, Jeju National University, Jeju, 63243, Republic of Korea;2. Laboratory of Comparative Animal Medicine, Division of Animal Life Science, Institute of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, 183-8509, Japan;3. Laboratory of Veterinary Molecular Pathology and Therapeutics, Division of Animal Life Science, Graduate School, Institute of Agriculture, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo, 183-8509, Japan |
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Abstract: | Gliosis including microgliosis and astrogliosis is a response to central nervous system inflammation. The purpose of this study was to evaluate whether olfactory bulbs are influenced by intranasal exposure to the detergent Triton X-100, a non-ionic surfactant. In this experiment, we measured olfactory function in mice based on the time needed to identify hidden pellets. Our results found that more time was needed to find the buried pellets by mice exposed to Triton X-100 compared with mice without Triton X-100 exposure, up to day 7. Histopathological examination revealed inflammatory cells in the olfactory mucosa and olfactory bulbs in mice treated with Triton X-100. Western blot analysis revealed significant downregulation of olfactory marker proteins in the olfactory mucosa and bulbs of mice after intranasal exposure to Triton X-100. In the olfactory bulbs of mice exposed to Triton X-100, microgliosis and astrogliosis were evident using immunohistochemistry. Cathepsin D was also upregulated in Iba-1-positive microglia/macrophages and GFAP-positive astrocytes in the olfactory bulbs of mice exposed to Triton X-100. In mice, Triton X-100 induced olfactory sensory neuron death in the nasal cavity and gliosis in olfactory bulbs with concurrent downregulation of olfactory marker protein expression, resulting in transient olfactory dysfunction. |
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Keywords: | Corresponding author at: Department of Veterinary Anatomy, College of Veterinary Medicine, Jeju National University, 102 Jejudaehakno, Jeju, 63243, Republic of Korea. CNS central nervous system GFAP glial fibrillary acidic protein Iba-1 ionized calcium-binding adapter molecule-1 OD optical density OMP olfactory marker protein PBS phosphate-buffered saline Gliosis Olfactory bulb Olfactory marker protein Cathepsin D Triton X-100 |
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