Kacprzak Victoria, Patel Neil A, Riley Elizabeth, Yu Lili, Yeh Jing-Ruey J, Zhdanova Irina V
Boston University School of Medicine, Lab of Sleep and Circadian Physiology, R-911, 72 E. Concord St., Boston, MA 02118, United States.
Massachusetts General Hospital, Cardiovascular Research Center, 149 13th St., 4.217, Charlestown, MA 02129, United States.
Pharmacol Biochem Behav. 2017 Jun;157:1-8. doi: 10.1016/j.pbb.2017.01.005. Epub 2017 Apr 10.
Changes in the expression of the dopamine transporter (DAT), or the sensitivity of dopamine receptors, are associated with aging and substance abuse and may underlie some of the symptoms common to both conditions. In this study, we explored the role of the dopaminergic system in the anxiogenic effects of aging and acute cocaine exposure by comparing the behavioral phenotypes of wild type (WT) and DAT knockout zebrafish (DAT-KO) of different ages. To determine the involvement of specific dopamine receptors in anxiety states, antagonists to D1 (SCH23390) and D2/D3 (sulpiride) were employed. We established that DAT-KO results in a chronic anxiety-like state, seen as an increase in bottom-dwelling and thigmotaxis. Similar effects were produced by aging and acute cocaine administration, both leading to reduction in DAT mRNA abundance (qPCR). Inhibition of D1 activity counteracted the anxiety-like effects associated with DAT deficit, independent of its origin. Inhibition of D2/D3 receptors reduced anxiety in young DAT-KO, and enhanced the anxiogenic effects of cocaine in WT, but did not affect aged WT or DAT-KO fish. These findings provide new evidence that the dopaminergic system plays a critical role in anxiety-like states, and suggest that adult zebrafish provide a sensitive diurnal vertebrate model for elucidating the molecular mechanisms of anxiety and a platform for anxiolytic drug screens.
多巴胺转运体(DAT)表达的变化或多巴胺受体的敏感性与衰老和药物滥用相关,可能是这两种情况共有的一些症状的潜在原因。在本研究中,我们通过比较不同年龄野生型(WT)和DAT基因敲除斑马鱼(DAT-KO)的行为表型,探讨了多巴胺能系统在衰老和急性可卡因暴露所致焦虑效应中的作用。为了确定特定多巴胺受体在焦虑状态中的作用,使用了D1(SCH23390)和D2/D3(舒必利)拮抗剂。我们发现DAT-KO会导致慢性焦虑样状态,表现为底栖行为和趋触性增加。衰老和急性给予可卡因也产生了类似的效果,两者均导致DAT mRNA丰度降低(qPCR)。抑制D1活性可抵消与DAT缺陷相关的焦虑样效应,无论其起源如何。抑制D2/D3受体可减轻年轻DAT-KO鱼的焦虑,并增强可卡因对WT鱼的致焦虑作用,但对老年WT或DAT-KO鱼没有影响。这些发现提供了新的证据,表明多巴胺能系统在焦虑样状态中起关键作用,并表明成年斑马鱼为阐明焦虑的分子机制提供了一个敏感的昼夜脊椎动物模型,也是抗焦虑药物筛选的平台。