Control of the binding of a vesamicol analog to the vesicular acetylcholine transporter

被引:11
作者
Clarizia, AD
Gomez, MV
Romano-Silva, MA
Parsons, SM
Prado, VF
Prado, MAM
机构
[1] Univ Fed Minas Gerais, Dept Farmacol, Lab Neurofarmacol, ICB, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Bioquim Imunol, Lab Neurofarmacol, ICB, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Calif Santa Barbara, Dept Chem, Santa Barbara, CA 93106 USA
关键词
acetylcholine; acetylcholine storage; synaptic vesicles; vesamicol; vesicular acetylcholine transporter;
D O I
10.1097/00001756-199909090-00016
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
4-AMINOBENZOVESAMICOL was used to test whether activation of protein kinase C protects the vesicular acetylcholine transporter from interaction with vesamicol-like drugs. The essentially irreversible vesamicol analog inhibits the release of newly synthesized [H-3]acetylcholine from stimulated hippocampal slices. Prior activation of protein kinase C with a phorbol ester prevented the inhibition of [3H]acetylcholine release, but activation of protein kinase C after the exposure to the irreversible analog did not prevent the effect of the drug. Binding of 4-aminobenzovesamicol in hippocampal synaptosomes, assayed using [H-3]vesamicol and back-titration, was decreased by activation of protein kinase C prior to analog exposure but not by activation subsequent to exposure. We propose that phosphorylation of the vesicular acetylcholine transporter prevents the binding of vesamicol-like drugs. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:2783 / 2787
页数:5
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