Robinson P J, Lovenberg W
Neurosci Lett. 1986 Jul 11;68(1):1-6. doi: 10.1016/0304-3940(86)90219-3.
Protein phosphorylation in intact synaptosomes is highly sensitive to alterations in calcium fluxes and was used to probe the possible mechanism of action of the calcium channel agonist BAY K 8644 and antagonists verapamil and nifedipine. These agents (at 1 microM) all increased the basal phosphorylation of a specific set of 4 synaptosomal phosphoproteins termed P139, P124, P96 and P60, but did not alter depolarization-dependent protein phosphorylation. The increases could not be explained by a direct stimulation of protein kinases and appears unrelated to the known effects of these drugs on K+-stimulated neurotransmitter release. This finding may reveal a possible new mechanism of action for drugs which interact with calcium channels.
完整突触体中的蛋白质磷酸化对钙通量的变化高度敏感,并被用于探究钙通道激动剂BAY K 8644以及拮抗剂维拉帕米和硝苯地平的可能作用机制。这些药物(浓度为1微摩尔)均增加了一组特定的4种突触体磷蛋白(称为P139、P124、P96和P60)的基础磷酸化水平,但并未改变去极化依赖性蛋白质磷酸化。这些增加不能用对蛋白激酶的直接刺激来解释,并且似乎与这些药物对钾离子刺激的神经递质释放的已知作用无关。这一发现可能揭示了与钙通道相互作用的药物的一种可能的新作用机制。