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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Casein kinase 1 enables nucleus accumbens amphetamine-induced locomotion by regulating AMPA receptor phosphorylation
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Casein kinase 1 enables nucleus accumbens amphetamine-induced locomotion by regulating AMPA receptor phosphorylation

机译:酪蛋白激酶1通过调节AMPA受体磷酸化使伏隔核安非他明诱导的运动

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摘要

The closely related 8 and s isoforms of the serine/threonine protein kinase casein kinase 1 (Csnki) have been implicated in the generation of psychostimulant-induced behaviors. In this study, we show that Csnki 8/s produces its effects on behavior by acting on the Darpp-32-PP1 signaling pathway to regulate AMPA receptor phosphorylation in the nucleus accumbens (NAcc). Inhibiting Csnki S/e in the NAcc with the selective inhibitor PF-670462 blocks amphetamine induced locomotion and its ability to increase phosphoryiation of Dar-pp-32 at S137 and T34, decrease PP1 activity and increase phosphorylation of the AMPA receptor subunit at S845,Consistent with these findings, preventing GluR1 phosphorylation with the alanine mutant GluR1 (S845A) reduces gluta-mate-evoked currents in cultured medium spiny neurons and blocks the locomotor activity produced by NAcc amphetamine. Thus, Csnki enables the locomotor and likely the incentive motivational effects of amphetamine by regulating Darrp-32-PP1-GlurR1{S845) signaling in the NAcc. As such, Csnki may be a critical target for intervention in the treatment of drug use disorders.
机译:丝氨酸/苏氨酸蛋白激酶酪蛋白激酶1(Csnki)的密切相关的8和s同工型与精神刺激药诱发的行为有关。在这项研究中,我们显示Csnki 8 / s通过作用于Darpp-32-PP1信号通路来调节伏伏核(NAcc)中的AMPA受体磷酸化,从而对行为产生影响。用选择性抑制剂PF-670462抑制NAcc中的Csnki S / e阻断苯丙胺诱导的运动,并增强S137和T34处Dar-pp-32的磷酸化,降低PP1活性并增加S845处AMPA受体亚基的磷酸化,与这些发现一致,用丙氨酸突变体GluR1(S845A)防止GluR1磷酸化可减少培养基中多刺神经元中谷氨酸诱发的电流,并阻止NAcc安非他明产生的运动活性。因此,Csnki通过调节NAcc中的Darrp-32-PP1-GlurR1 {S845)信号传导来实现苯丙胺的运动,并可能产生苯丙胺的激励动机。因此,Csnki可能是干预药物滥用疾病的关键目标。

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