Uchikawa T, Kiuchi Y, Yura A, Nakachi N, Yamazaki Y, Yokomizo C, Oguchi K
Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
J Neurochem. 1995 Nov;65(5):2065-71. doi: 10.1046/j.1471-4159.1995.65052065.x.
We studied effects of Ca2+ in the incubation medium on [3H]dopamine ([3H]DA) uptake by rat striatal synaptosomes. Both the duration of the preincubation period with Ca2+ (0-30 min) and Ca2+ concentration (0-10 mM) in Krebs-Ringer medium affected [3H]DA uptake by the synaptosomes. The increase was maximal at a concentration of 1 mM Ca2+ after a 10-min preincubation (2.4 times larger than the uptake measured without preincubation), which reflected an increase in Vmax of the [3H]DA uptake process. On the other hand, [3H]DA uptake decreased rapidly after addition of ionomycin in the presence of 1 mM Ca2+. The Ca(2+)-dependent enhancement of the uptake was still maintained after washing synaptosomes with Ca(2+)-free medium following preincubation with 1 mM Ca2+. Protein kinase C inhibitors did not affect apparently Ca(2+)-dependent enhancement of the uptake, whereas 1(-)[N,O-bis(1,5-isoquinolinesulfonyl)-N-methyl-L- tyrosyl]-4-phenylpiperazine (KN-62; a Ca2+/calmodulin-dependent kinase II inhibitor) and wortmannin (a myosin light chain kinase inhibitor) significantly reduced it. Inhibitory effects of KN-62 and wortmannin appeared to be additive. N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride (W-7; a calmodulin antagonist) also remarkably inhibited the enhancement. These results suggest that Ca(2+)-dependent enhancement of [3H]DA uptake is mediated by activation of calmodulin-dependent protein kinases.
我们研究了孵育培养基中的Ca2+对大鼠纹状体突触体摄取[3H]多巴胺([3H]DA)的影响。在Krebs-Ringer培养基中,预孵育Ca2+的时间(0 - 30分钟)和Ca2+浓度(0 - 10 mM)均会影响突触体对[3H]DA的摄取。预孵育10分钟后,当Ca2+浓度为1 mM时摄取量增加最大(比未预孵育时测得的摄取量高2.4倍),这反映了[3H]DA摄取过程中Vmax的增加。另一方面,在1 mM Ca2+存在的情况下加入离子霉素后,[3H]DA摄取迅速下降。用不含Ca2+的培养基洗涤突触体后,预孵育1 mM Ca2+所产生的Ca2+依赖性摄取增强作用仍得以维持。蛋白激酶C抑制剂对Ca2+依赖性摄取增强作用无明显影响,而1-[-N,O-双(1,5-异喹啉磺酰基)-N-甲基-L-酪氨酰]-4-苯基哌嗪(KN-62;一种Ca2+/钙调蛋白依赖性激酶II抑制剂)和渥曼青霉素(一种肌球蛋白轻链激酶抑制剂)则能显著降低该作用。KN-62和渥曼青霉素的抑制作用似乎具有相加性。N-(6-氨基己基)-5-氯-1-萘磺酰胺盐酸盐(W-7;一种钙调蛋白拮抗剂)也能显著抑制这种增强作用。这些结果表明,[3H]DA摄取的Ca2+依赖性增强是由钙调蛋白依赖性蛋白激酶的激活介导的。