Singer Bryan F, Bubula Nancy, Przybycien-Szymanska Magdalena M, Li Dongdong, Vezina Paul
Department of Psychology, University of Michigan, Ann Arbor, MI, USA; Committee on Neurobiology, University of Chicago, Chicago, IL, USA.
Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA.
Eur Neuropsychopharmacol. 2016 Nov;26(11):1836-1842. doi: 10.1016/j.euroneuro.2016.09.639. Epub 2016 Oct 6.
Drug-paired stimuli rapidly enlarge dendritic spines in the nucleus accumbens (NAcc). While increases in spine size and shape are supported by rearrangement of the actin cytoskeleton and facilitate the synaptic expression of AMPA-type glutamate receptors, it remains unclear whether drug-related stimuli can influence signaling pathways known to regulate these changes in spine morphology. These pathways were studied in rats trained on a discrimination learning paradigm using subcellular fractionation and protein immunoblotting to isolate proteins within dendritic spine compartments in the NAcc shell. An open field chamber was repeatedly associated with amphetamine in one group (Paired) and explicitly unpaired with amphetamine in another (Unpaired). Rats in a third group were exposed to the open field but never administered amphetamine (Control). When administered saline and returned to the open field one week later, Paired rats as expected displayed a conditioned locomotor response relative to rats in the other two groups. NAcc shell tissues were harvested immediately after this 30-minute test. Re-exposing Paired rats to the drug-paired excitatory context significantly decreased p-GluA2(S880), an effect consistent with reduced internalization of this subunit and increased spine proliferation in these rats. In contrast, re-exposing Unpaired rats to the drug-unpaired context, capable of inhibiting conditioned responding in these animals, significantly decreased levels of both actin binding protein Arp2/3 and p-cofilin, consistent with spine volatility, shrinkage, and inhibition of spine proliferation in these rats. These findings show that contextual stimuli previously associated with either the presence or absence of amphetamine differentially regulate cytoskeletal signaling pathways in the NAcc.
与药物配对的刺激会迅速增大伏隔核(NAcc)中的树突棘。虽然肌动蛋白细胞骨架的重排支持了树突棘大小和形状的增加,并促进了AMPA型谷氨酸受体的突触表达,但药物相关刺激是否能影响已知调节这些树突棘形态变化的信号通路仍不清楚。在接受辨别学习范式训练的大鼠中,利用亚细胞分级分离和蛋白质免疫印迹法分离NAcc壳中树突棘隔室内的蛋白质,对这些信号通路进行了研究。在一组中,旷场箱与苯丙胺反复配对(配对组),在另一组中与苯丙胺明确不配对(非配对组)。第三组大鼠暴露于旷场但从未给予苯丙胺(对照组)。当给予生理盐水并在一周后返回旷场时,正如预期的那样,配对组大鼠相对于其他两组大鼠表现出条件性运动反应。在这个30分钟的测试后,立即采集NAcc壳组织。将配对组大鼠重新暴露于与药物配对的兴奋性环境中,显著降低了p-GluA2(S880),这一效应与该亚基内化减少以及这些大鼠树突棘增殖增加一致。相比之下,将非配对组大鼠重新暴露于与药物不配对的环境中,这种环境能够抑制这些动物的条件反应,显著降低了肌动蛋白结合蛋白Arp2/3和p-丝切蛋白的水平,这与这些大鼠树突棘的波动性、收缩以及树突棘增殖的抑制一致。这些发现表明,先前与苯丙胺存在或不存在相关的环境刺激对NAcc中的细胞骨架信号通路有不同的调节作用。