Environmental enrichment during forced abstinence from cocaine self-administration opposes gene network expression changes associated with the incubation effect

被引:16
作者
Powell, Gregory L. [1 ]
Vannan, Annika [1 ]
Bastle, Ryan M. [1 ,4 ]
Wilson, Melissa A. [1 ,2 ]
Dell'Orco, Michela [3 ]
Perrone-Bizzozero, Nora, I [3 ]
Neisewander, Janet L. [1 ]
机构
[1] Arizona State Univ, Sch Life Sci, POB 874501, Tempe, AZ 85287 USA
[2] Arizona State Univ, Ctr Evolut & Med, Tempe, AZ 85287 USA
[3] Univ New Mexico, Sch Med, Dept Neurosci, Albuquerque, NM 87131 USA
[4] Icahn Sch Med Mt Sinai, Nash Family Dept Neurosci, New York, NY 10029 USA
关键词
INTEGRIN-LINKED KINASE; RAT PREFRONTAL CORTEX; NUCLEUS-ACCUMBENS; SEEKING BEHAVIOR; MESSENGER-RNA; NICOTINE; NEUROGENESIS; DECREASES; ADDICTION; DOPAMINE;
D O I
10.1038/s41598-020-67966-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Environmental enrichment (EE) is a robust intervention for reducing cocaine-seeking behaviors in animals when given during forced abstinence. However, the mechanisms that underlie these effects are not well-established. We investigated the adult male rat transcriptome using RNA-sequencing (RNA-seq) following differential housing during forced abstinence from cocaine self-administration for either 1 or 21 days. Enriched, 21-day forced abstinence rats displayed a significant reduction in cocaine-seeking behavior compared to rats housed in isolation. RNA-seq of the nucleus accumbens shell revealed hundreds of differentially regulated transcripts between rats of different forced abstinence length and housing environment, as well as within specific contrasts such as enrichment (isolated 21 days vs. enriched 21 days) or incubation (isolated 1 day vs. isolated 21 days). Ingenuity Pathway Analysis affirmed several pathways as differentially enriched based on housing condition and forced abstinence length including RELN, the Eif2 signaling pathway, synaptogenesis and neurogenesis pathways. Numerous pathways showed upregulation with incubation, but downregulation with EE, suggesting that EE may prevent or reverse changes in gene expression associated with protracted forced abstinence. The findings reveal novel candidate mechanisms involved in the protective effects of EE against cocaine seeking, which may inform efforts to develop pharmacological and gene therapies for treating cocaine use disorders. Furthermore, the finding that EE opposes multiple pathway changes associated with incubation of cocaine seeking strongly supports EE as a therapeutic intervention and suggests EE is capable of preventing or reversing the widespread dysregulation of signaling pathways that occurs during cocaine forced abstinence.
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页数:15
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