首页> 外文会议>International Joint Conference on Neural Networks;IJCNN 2009 >A Computational study of pre-synaptic re-uptake of dopamine on phosphorylation of DARPP-32
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A Computational study of pre-synaptic re-uptake of dopamine on phosphorylation of DARPP-32

机译:突触前再摄取多巴胺对DARPP-32磷酸化的计算研究

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. The complex of adenylate cyclase activates and increases the intracellular levels of cAMP and thereby stimulating cAMP dependent protein kinase and increasing the state of phosphorylation of DARPP-32 (dopamine and cyclic AMP-regulated phosphoprotein, M, = 32,000). DARPP-32 plays an important role in autophosphorylation of calcium calmodulin dependent protein kinaseII (CaMKII) which is crucial for prolongation of long term potentiation (LTP). Here we verified the effect of pre-synaptic re-uptake of dopamine by dopamine transporter on the phosphorylation of DARPP-32 and found that the phosphorylation of DARPP-32 is unaffected by pre-synaptic re-uptake. Further we have seen that the DARPP-32 phosphorylation does not change with the change in the DA or D1R concentrations.
机译:。腺苷酸环化酶的复合物激活并增加细胞内cAMP的水平,从而刺激cAMP依赖性蛋白激酶并增加DARPP-32的磷酸化状态(多巴胺和环AMP调节的磷蛋白,M = 32,000)。 DARPP-32在钙调蛋白依赖性蛋白激酶II(CaMKII)的自磷酸化中起重要作用,这对于延长长期增强(LTP)至关重要。在这里,我们验证了由多巴胺转运蛋白突触前重新摄取多巴胺对DARPP-32磷酸化的影响,并发现DARPP-32的磷酸化不受突触前重新摄取的影响。此外,我们已经看到,DARPP-32磷酸化不会随DA或D1R浓度的变化而变化。

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