4.8 Article

A Causative Link Between Inner Ear Defects and Long-Term Striatal Dysfunction

Journal

SCIENCE
Volume 341, Issue 6150, Pages 1120-1123

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1240405

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Funding

  1. Tourette Syndrome Association
  2. NIH [R21NS073761, R01MH083804]
  3. Deutsche Forschungsgemeinschaft [HU 800/5-1]

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There is a high prevalence of behavioral disorders that feature hyperactivity in individuals with severe inner ear dysfunction. What remains unknown is whether inner ear dysfunction can alter the brain to promote pathological behavior. Using molecular and behavioral assessments of mice that carry null or tissue-specific mutations of Slc12a2, we found that inner ear dysfunction causes motor hyperactivity by increasing in the nucleus accumbens the levels of phosphorylated adenosine 3',5'-monophosphate response element-binding protein (pCREB) and phosphorylated extracellular signal-regulated kinase (pERK), key mediators of neurotransmitter signaling and plasticity. Hyperactivity was remedied by local administration of the pERK inhibitor SL327. These findings reveal that a sensory impairment, such as inner ear dysfunction, can induce specific molecular changes in the brain that cause maladaptive behaviors, such as hyperactivity, that have been traditionally considered exclusively of cerebral origin.

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