
There is strong evidence for a purinergic signalling system in the inner ear which regulates auditory sensitivity. This study describes the terminating mechanism for purinergic signalling in the cochlear endolymphatic compartment via ecto-nucleotidases. Exogenous ATP was introduced into the scala media (SM) of the isolated, perfused guinea-pig cochlea, and the effluent was assayed for the adenine nucleotide metabolites by reverse-phase HPLC. Tissue viability was confirmed by fluorescence imaging of cochlear tissues. Extracellular ATP degradation to adenosine was Ca2+/Mg2+ dependent, and was not affected by inhibitors of intracellular ATPases and non-specific alkaline phosphatase. High azide concentration (5 mM) and suramin produced an inhibitory effect on ATP hydrolysis, consistent with inhibition of E-type ATPase activity. The Vmax of ATP hydrolysis (2564 mumol min-1 SM-1) was indicative of high ecto-ATPase activity. Our results support the role of ecto-nucleotidases as a principal mechanism for termination of purinergic signalling within SM, a compartment of the cochlea showing considerable P2X receptor expression.
Adenosine Triphosphatases, Male, Adenosine, Cell Survival, Receptors, Purinergic P2, Guinea Pigs, Suramin, In Vitro Techniques, Alkaline Phosphatase, Cochlea, Lymphatic System, Perfusion, Adenosine Triphosphate, Animals, Female, Ca(2+) Mg(2+)-ATPase, Signal Transduction
Adenosine Triphosphatases, Male, Adenosine, Cell Survival, Receptors, Purinergic P2, Guinea Pigs, Suramin, In Vitro Techniques, Alkaline Phosphatase, Cochlea, Lymphatic System, Perfusion, Adenosine Triphosphate, Animals, Female, Ca(2+) Mg(2+)-ATPase, Signal Transduction
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