Department of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, Columbia, South Carolina, USA.
PLoS One. 2012;7(8):e44149. doi: 10.1371/journal.pone.0044149. Epub 2012 Aug 31.
Exposure within an environmental enrichment paradigm results in neurobiological adaptations and decreases the baseline of locomotor activity. The current study determined activation of DARPP-32 (dopamine- and cAMP-regulated phosphoprotein-32) and CREB (cAMP response element binding protein), and locomotor activity in rats raised in enriched (EC), impoverished (IC), and standard (SC) conditions following repeated administration of nicotine or saline. In the saline-control group, the basal phosphorylation state of DARPP-32 at Threonine-34 site (pDARPP-32 Thr34) in the prefrontal cortex (PFC) was lower in EC compared to IC and SC rats, which was positively correlated with their respective baseline activities. While nicotine (0.35 mg/kg, freebase) produced locomotor sensitization across all housing conditions when the nicotine-mediated locomotor activity was expressed as a percent change from their respective saline control, EC rats displayed greater sensitization to nicotine than IC and SC rats. Consistent with the behavioral findings, repeated nicotine injection increased pDARPP-32 Thr34 in PFC of EC and IC rats and in nucleus accumbens of EC rats; however, the magnitude of change from saline control in nicotine-induced enhancement of pDARPP-32 Thr34 in PFC was strikingly increased in EC rats relative to IC rats. Moreover, EC rats had lower basal phosphorylation levels of CREB at serine 133 in PFC and nucleus accumbens compared to IC and SC rats, whereas the nicotine-induced increase in phosphorylated CREB-Ser133 was more pronounced in PFC of EC rats relative to IC and SC rats. Collectively, these findings suggest innovative insights into advancing our understanding of the molecular mechanisms of enrichment-induced changes in the motivational effects of nicotine, and aiding in the identification of new therapeutic strategies for tobacco smokers.
在环境丰富化范式中暴露会导致神经生物学适应,并降低运动活动的基线。本研究确定了在重复给予尼古丁或生理盐水后,在丰富(EC)、贫乏(IC)和标准(SC)条件下饲养的大鼠中的 DARPP-32(多巴胺和 cAMP 调节的磷酸蛋白-32)和 CREB(cAMP 反应元件结合蛋白)的激活以及运动活动。在生理盐水对照组中,前额叶皮层(PFC)中 DARPP-32 在苏氨酸 34 位(pDARPP-32 Thr34)的基础磷酸化状态在 EC 大鼠中低于 IC 和 SC 大鼠,这与其各自的基线活动呈正相关。虽然尼古丁(0.35mg/kg,游离碱)在所有饲养条件下都产生了运动敏化作用,当尼古丁介导的运动活动表示为相对于各自生理盐水对照的百分比变化时,EC 大鼠对尼古丁的敏化作用大于 IC 和 SC 大鼠。与行为发现一致,重复给予尼古丁注射增加了 EC 和 IC 大鼠 PFC 以及 EC 大鼠伏隔核中的 pDARPP-32 Thr34;然而,与 IC 大鼠相比,EC 大鼠中尼古丁诱导的 pDARPP-32 Thr34 增强从生理盐水对照中变化的幅度明显增加。此外,EC 大鼠 PFC 和伏隔核中的 CREB 丝氨酸 133 的基础磷酸化水平低于 IC 和 SC 大鼠,而 EC 大鼠 PFC 中磷酸化 CREB-Ser133 的增加更为明显与 IC 和 SC 大鼠相比。总的来说,这些发现为深入了解环境丰富化诱导的尼古丁动机效应变化的分子机制提供了新的见解,并有助于为吸烟者确定新的治疗策略。