4.0 Article

Distinct patterns of ΔFosB induction in brain by drugs of abuse

期刊

SYNAPSE
卷 62, 期 5, 页码 358-369

出版社

WILEY-LISS
DOI: 10.1002/syn.20500

关键词

cocaine; morphine; ethanol; Delta(9)-THC; striatum; nucleus accumbens

资金

  1. NIDA NIH HHS [R01 DA003672-24A1, R01 DA003672] Funding Source: Medline

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The transcription factor Delta FosB accumulates and persists in brain in response to chronic stimulation. This accumulation after chronic exposure to drugs of abuse has been demonstrated previously by Western blot most dramatically in striatal regions, including dorsal striatum (caudate/putamen) and nucleus accumbens. In the present study, we used immunohistochemistry to define with greater anatomical precision the induction of Delta FosB throughout the rodent brain after chronic drug treatment. We also extended previous research involving cocaine, morphine, and nicotine to two additional drugs of abuse, ethanol and Delta(9)-tetrahydrocannabinol (Delta(9)-THC, the active ingredient in marijuana). We show here that chronic, but not acute, administration of each of four drugs of abuse, cocaine, morphine, ethanol, and Delta(9)-THC, robustly induces Delta FosB in nucleus accumbens, although different patterns in the core vs. shell subregions of this nucleus were apparent for the different drugs. The drugs also differed in their degree of Delta FosB induction in dorsal striatum. In addition, all four drugs induced Delta FosB in prefrontal cortex, with the greatest effects observed with cocaine and ethanol, and all of the drugs induced Delta FosB to a small extent in amygdala. Furthermore, all drugs induced Delta FosB in the hippocampus, and, with the exception of ethanol, most of this induction was seen in the dentate. Lower levels of Delta FosB induction were seen in other brain areas in response to a particular drug treatment. These findings provide further evidence that induction of Delta FosB in nucleus accumbens is a common action of virtually all drugs of abuse and that, beyond nucleus accumbens, each drug induces Delta FosB in a region-specific manner in brain.

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