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Masticatory dysfunction and neuroactive opioids
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K. YAMADA1, H. PARK1, K. SASAGURI2, T. YAMAMOTO3, M. ONOZUKA2, and S. SATO2, 1Kanagawa Dental College, Yokosuka, Japan, 2Kanagawa Dental College, Japan, 3Kanagawa Dental College, Yokosuka Kanagawa, Japan | Objectives: We investigated the effects of masticatory dysfunction on endogenous opioids in the cerebral limbic system and hypothalamus, and examined the possible association with stress using a corticosterone synthesis inhibitor, metyrapone. Methods: Masticatory dysfunction was made by raising the height of mouse molar with a dental resin. Immunohistochemistry was performed according to the ABC method. A group of dysfunctional mice was pretreated with metyrapone. Results: Among tested opioids, dynorphin-A immunoreactive intensity and immunopositive cell number were increased in both the amygdala (especially in the central amygdala) and hypothalamus (especially in the paraventricular hypothalamic nucleus), in comparison with sham-operated mice. Pretreatment of metyrapone seemed to prohibit these changes in the central amygdala, but not in the hypothalamus. Conclusion: The present data suggest the involvement of masticatory dysfunction in the emotional integration processes that may be coupled with an endogenous opioid, dynorphin-A in the amygdala and hypothalamus. Since corticosterone mediates stress response, the present results also suggest the involvement of stress with the increased dynorphin-A-like immunoreactivity in the amygdala. This work was supported by an Open Research Center subsidy (H18) from MEXT. | Seq #213 - Neuroscience/TMJ Posters III 2:00 PM-3:15 PM, Friday, July 4, 2008 Metro Toronto Convention Centre Exhibit Hall D-E |
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