Copeland B J, Vogelsberg V, Neff N H, Hadjiconstantinou M
Neuroscience Program, Ohio State University, College of Medicine, Columbus, USA.
J Pharmacol Exp Ther. 1996 Jun;277(3):1527-32.
Incubation with either of the protein kinase C activators phorbol 12-myristate 13-acetate (PMA) and sn-1,2 dioctanoylglycerol (DiC8) decreased the uptake of dopamine into striatal synaptosomes, whereas the inactive phorbol ester 4 alpha-PMA had no effect. Washout of PMA and DiC8 failed to reverse the decrease in uptake. Kinetic analysis showed a decrease in the apparent V(max) for the transporter without changes in the K(m). Neither PMA nor DiC8 affected mazindol binding to the dopamine transporter. Preincubation with the protein kinase inhibitor staurosporine prevented the DiC8-induced decrease of dopamine uptake. Furthermore, the protein phosphatase inhibitor okadaic acid decreased dopamine uptake by itself and enhanced the DiC8-induced reduction of uptake. These findings support a role for protein kinase C in modulating dopamine transporter activity.
用蛋白激酶C激活剂佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)和sn - 1,2 - 二辛酰甘油(DiC8)中的任何一种进行孵育,均可降低多巴胺向纹状体突触体的摄取,而无活性的佛波酯4α - PMA则无此作用。洗脱PMA和DiC8未能逆转摄取的降低。动力学分析表明,转运体的表观V(max)降低,而K(m)无变化。PMA和DiC8均不影响马吲哚与多巴胺转运体的结合。用蛋白激酶抑制剂星形孢菌素预孵育可防止DiC8诱导的多巴胺摄取降低。此外,蛋白磷酸酶抑制剂冈田酸自身可降低多巴胺摄取,并增强DiC8诱导的摄取减少。这些发现支持蛋白激酶C在调节多巴胺转运体活性中起作用。