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The Neuroscientist
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*Substance via MeSH
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*Neurologic Diseases
*Taste and Smell Disorders
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Article

Defects in Tongue Papillae and Taste Sensation Indicate a Problem with Neurotrophic Support in Various Neurological Diseases

John Gardiner*, Deborah Barton, Jessica May Vanslambrouck, Filip Braet, David Hall, Jan Marc, and Robyn Overall

* To whom correspondence should be addressed. E-mail: jgardiner{at}mail.usyd.edu.au.


   Abstract
Neurotrophic support of developing neurons by neurotrophins is of critical importance in the development of fungiform papillae and taste buds. A number of neurological disorders show a decrease or increase in fungiform papillae or taste sensation. These can be grouped into disorders with reduced papillae (Machado-Joseph disease, Stüve-Wiedemann syndrome, familial dysautonomia, dystonia musculorum, and Behçet’s disease) and those with taste defects only (Alzheimer’s disease, Huntington’s disease, hereditary sensory and autonomic neuropathy type IV, and diabetes mellitus). In addition, Parkinson’s disease results in increased taste sensation. Here, we hypothesize that the main problem in these disorders is either not enough or too much neurotrophic support. Proneurotrophic drugs such as some antidepressants and aldose reductase inhibitors may prove useful in the treatment of these sensory and central nervous system disorders. Similarly, antineurotrophic drugs may also be useful in Parkinson’s disease. Here we show that the protein involved in familial dysautonomia, IKAP, localizes to keratin filaments in HeLa cells, suggesting a role for the keratin cytoskeleton in neurotrophic support. NEUROSCIENTIST XX(X):xx–xx, XXXX. DOI: 10.1177/1073858407312382

First published on February 12, 2008, doi:10.1177/1073858407312382

The Neuroscientist 2008;14:240.

A more recent version of this article appeared on June 1, 2008


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