Singer Bryan F, Neugebauer Nichole M, Forneris Justin, Rodvelt Kelli R, Li Dongdong, Bubula Nancy, Vezina Paul
Committee on Neurobiology, The University of Chicago, Chicago, IL, USA.
Department of Psychiatry and Behavioral Neuroscience, The University of Chicago, Chicago, IL, USA.
Neuropharmacology. 2014 Oct;85:243-52. doi: 10.1016/j.neuropharm.2014.05.033. Epub 2014 Jun 2.
Intermittent systemic exposure to psychostimulants leads to several forms of long-lasting behavioral plasticity including nonassociative sensitization and associative conditioning. In the nucleus accumbens (NAcc), the protein serine/threonine kinase cyclin-dependent kinase 5 (Cdk5) and its phosphorylation target, the guanine-nucleotide exchange factor kalirin-7 (Kal7), may contribute to the neuroadaptations underlying the formation of conditioned associations. Pharmacological inhibition of Cdk5 in the NAcc prevents the increases in dendritic spine density normally observed in this site following repeated cocaine. Mice lacking the Kal7 gene display similar effects. As increases in spine density may relate to the formation of associative memories and both Cdk5 and Kal7 regulate the generation of spines following repeated drug exposure, we hypothesized that either inhibiting Cdk5 or preventing its phosphorylation of Kal7 in the NAcc may prevent the induction of drug conditioning. In the present experiments, blockade in rats of NAcc Cdk5 activity with roscovitine (40 nmol/0.5 μl/side) prior to each of 4 injections of amphetamine (1.5 mg/kg; i.p.) prevented the accrual of contextual locomotor conditioning but spared the induction of locomotor sensitization as revealed on tests conducted one week later. Similarly, transient viral expression in the NAcc exclusively during amphetamine exposure of a threonine-alanine mutant form of Kal7 [mKal7(T1590A)] that is not phosphorylated by Cdk5 also prevented the accrual of contextual conditioning and spared the induction of sensitization. These results indicate that signaling via Cdk5 and Kal7 in the NAcc is necessary for the formation of context-drug associations, potentially through the modulation of dendritic spine dynamics in this site.
间歇性全身暴露于精神兴奋剂会导致多种形式的持久行为可塑性,包括非联想性敏感化和联想性条件反射。在伏隔核(NAcc)中,蛋白丝氨酸/苏氨酸激酶细胞周期蛋白依赖性激酶5(Cdk5)及其磷酸化靶点鸟嘌呤核苷酸交换因子卡里林-7(Kal7),可能参与了条件性联想形成背后的神经适应性变化。对NAcc中Cdk5进行药理抑制可阻止在反复给予可卡因后该部位通常观察到的树突棘密度增加。缺乏Kal7基因的小鼠表现出类似的效应。由于树突棘密度的增加可能与联想记忆的形成有关,并且Cdk5和Kal7都在反复药物暴露后调节树突棘的生成,我们推测,抑制NAcc中的Cdk5或阻止其对Kal7的磷酸化可能会阻止药物条件反射的诱导。在本实验中,在大鼠每次注射4次苯丙胺(1.5mg/kg;腹腔注射)之前,用罗司维汀(40nmol/0.5μl/侧)阻断NAcc的Cdk5活性,可阻止情境性运动条件反射的形成,但不影响运动敏感化的诱导,这在一周后的测试中得到了证实。同样,仅在苯丙胺暴露期间在NAcc中瞬时病毒表达一种不被Cdk5磷酸化的苏氨酸-丙氨酸突变形式的Kal7 [mKal7(T1590A)],也可阻止情境性条件反射的形成,且不影响敏感化的诱导。这些结果表明,NAcc中通过Cdk5和Kal7的信号传导对于情境-药物联想的形成是必要的,这可能是通过调节该部位的树突棘动力学实现的。