Cowell R M, Kantor L, Hewlett G H, Frey K A, Gnegy M E
Neuroscience Program, University of Michigan School of Medicine, Ann Arbor, MI, USA.
Eur J Pharmacol. 2000 Feb 11;389(1):59-65. doi: 10.1016/s0014-2999(99)00828-6.
We have reported that inhibition of protein kinase C blocks the Ca(2+)-independent reverse transport of dopamine mediated by amphetamine. In this study we investigated whether activation of protein kinase C by 12-O-tetradecanoyl phorbol-13-acetate (TPA) would mediate dopamine release through the plasmalemmal dopamine transporter. TPA, at 250 nM, increased the release of dopamine from rat striatal slices and synaptosomes while the inactive phorbol ester, 4alpha-phorbol, was ineffective. The TPA-mediated dopamine release was independent of extracellular calcium and was blocked by a selective protein kinase C inhibitor, Ro31-8220. The dopamine transporter antagonists, cocaine and GBR 12935 blocked the TPA-mediated dopamine release. In addition, cocaine blocked TPA-mediated phosphorylation of the plasmalemmal dopamine transporter. These results suggest that activation of protein kinase C results in reverse transport of dopamine through the plasmalemmal dopamine transporter and the phosphorylated substrate could be the dopamine transporter.
我们曾报道,蛋白激酶C的抑制可阻断由苯丙胺介导的多巴胺的非钙依赖性逆向转运。在本研究中,我们调查了12-O-十四烷酰佛波醇-13-乙酸酯(TPA)对蛋白激酶C的激活是否会通过质膜多巴胺转运体介导多巴胺释放。250 nM的TPA可增加大鼠纹状体切片和突触体中多巴胺的释放,而无活性的佛波酯4α-佛波醇则无此作用。TPA介导的多巴胺释放不依赖细胞外钙,并被选择性蛋白激酶C抑制剂Ro31-8220阻断。多巴胺转运体拮抗剂可卡因和GBR 12935可阻断TPA介导的多巴胺释放。此外,可卡因可阻断TPA介导的质膜多巴胺转运体的磷酸化。这些结果表明,蛋白激酶C的激活导致多巴胺通过质膜多巴胺转运体进行逆向转运,且磷酸化底物可能是多巴胺转运体。