website: 86th General Session & Exhibition of the IADR

ABSTRACT: 2222  

Masticatory dysfunction and neuroactive opioids

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.

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