Effect of Protein Kinase C Activation on the Release of [3H]Acetylcholine in the Presence of Vesamicol


Address correspondence to Dr. M. A. M. Prado at Laboratório de Neurofarmacologia, Departamento de Farmacologia, ICB-UFMG, Av. Antonio Carlos, 6627, 31270-901 Belo Horizonte, MG, Brasil.


Abstract: The present work tested whether pharmacological activation of protein kinase C (PKC) influences the release of [3H]-acetylcholine ([3H]ACh) synthesized in the presence of vesamicol, an inhibitor of the vesicular acetylcholine transporter (VAChT). Newly synthesized [3H]ACh was released from hippocampal slices by field stimulation (15 Hz) in the absence of vesamicol, but as expected [3H]ACh synthesized during exposure to vesamicol was not released significantly by stimulation. Treatment of slices with the PKC activator phorbol myristate acetate (PMA) decreased the inhibitory effect of vesamicol on [3H]ACh release. The effect of PMA was dose-dependent, was sensitive to calphostin C, a PKC-selective inhibitor, and could not be mimicked by α-PMA, an inactive phorbol ester. PMA did not alter the release of [3H]ACh in the absence of vesamicol, suggesting that the site of PKC action could be related to the VAChT. In agreement with this observation, immunoprecipitation of VAChT from 32P-labeled synaptosomes showed that phosphorylation occurs and that incorporation of 32P in the VAChT protein increases in the presence of PMA. We suggest that PKC alters the output of [3H]ACh formed in the presence of vesamicol and also provide circumstantial evidence for a role of phosphorylation of VAChT in this process.

Abbreviations used: ACh, acetylcholine; HC-3, hemicholinium-3; PKC, protein kinase C; PMA, phorbol myristate acetate; VAChT, vesicular acetylcholine transporter; vesamicol, 2-(4-phenylpiperidino)cyclohexanol.