Role of protein kinase C in the release of [3H]acetylcholine from myenteric plexus treated with vesamicol

被引:8
作者
Clarizia, AD [1 ]
Romano-Silva, MA [1 ]
Prado, VF [1 ]
Gomez, MV [1 ]
Prado, MAM [1 ]
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Farmacol Bioquim Imunol, Lab Neurofarmacol, BR-30161 Belo Horizonte, MG, Brazil
关键词
acetylcholine release; vesamicol; vesicular acetylcholine transporter; synaptic vesicles; protein kinase C; ouabain;
D O I
10.1016/S0304-3940(98)00143-8
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The present experiments investigated the release of [3H]acetylcholine ([H-3]ACh) from the guinea pig myenteric plexus treated with 2-(4-phenylpiperidino)cyclohexanol (vesamicol), a drug that impairs ACh accumulation by synaptic vesicles. Ouabain, an Na+-K+ ATPase inhibitor, released [3H]ACh synthesised in the presence of (-)-vesamicol, while electrical field stimulation or KCl depolarisation were not effective to release the transmitter in this condition. The effect of ouabain was Ca2+-dependent and in the presence of (-)-vesamicol it was blocked by calphostin C, an inhibitor of protein kinase C (PKC). In addition, stimulation of kinase C activity by a phorbol ester, but not by its inactive isomer, prevented (-)-vesamicol from interfering with the release of [H-3]ACh in electrically-stimulated myenteric plexus, similar to the effect of ouabain. We conclude that release of [H-3]ACh induced by ouabain in the presence of (-)-vesamicol depends on PKC activation. (C) 1998 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:115 / 117
页数:3
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