Modeling consequences of prolonged strong unpredictable stress in zebrafish: Complex effects on behavior and physiology

斑马鱼 慢性应激 达尼奥 原肌球蛋白受体激酶B 生物 神经科学 树突棘 胶质纤维酸性蛋白 氟西汀 生物标志物 神经营养因子 受体 免疫学 基因 海马结构 免疫组织化学 血清素 生物化学
作者
Cai Song,Bai-Ping Liu,Yongping Zhang,Zhilan Peng,JiaJia Wang,Adam D. Collier,David J. Echevarria,Katerina V. Savelieva,Robert F. Lawrence,Christopher S. Rex,Darya A. Meshalkina,Allan V. Kalueff
出处
期刊:Progress in Neuro-psychopharmacology & Biological Psychiatry [Elsevier]
卷期号:81: 384-394 被引量:91
标识
DOI:10.1016/j.pnpbp.2017.08.021
摘要

Chronic stress is the major pathogenetic factor of human anxiety and depression. Zebrafish (Danio rerio) have become a novel popular model species for neuroscience research and CNS drug discovery. The utility of zebrafish for mimicking human affective disorders is also rapidly growing. Here, we present a new zebrafish model of clinically relevant, prolonged unpredictable strong chronic stress (PUCS). The 5-week PUCS induced overt anxiety-like and motor retardation-like behaviors in adult zebrafish, also elevating whole-body cortisol and proinflammatory cytokines - interleukins IL-1β and IL-6. PUCS also elevated whole-body levels of the anti-inflammatory cytokine IL-10 and increased the density of dendritic spines in zebrafish telencephalic neurons. Chronic treatment of fish with an antidepressant fluoxetine (0.1mg/L for 8days) normalized their behavioral and endocrine phenotypes, as well as corrected stress-elevated IL-1β and IL-6 levels, similar to clinical and rodent data. The CNS expression of the bdnf gene, the two genes of its receptors (trkB, p75), and the gfap gene of glia biomarker, the glial fibrillary acidic protein, was unaltered in all three groups. However, PUCS elevated whole-body BDNF levels and the telencephalic dendritic spine density (which were corrected by fluoxetine), thereby somewhat differing from the effects of chronic stress in rodents. Together, these findings support zebrafish as a useful in-vivo model of chronic stress, also calling for further cross-species studies of both shared/overlapping and distinct neurobiological responses to chronic stress.
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