Nestler Eric J
Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Eur J Pharmacol. 2015 Apr 15;753:66-72. doi: 10.1016/j.ejphar.2014.10.034. Epub 2014 Nov 7.
ΔFosB is a member of the Fos family of transcription factors. While other family members are induced rapidly but transiently in response to a host of acute stimuli, ΔFosB is unique in that it accumulates in response to repeated stimulation due to its unusual protein stability. Such prolonged induction of ΔFosB, within nucleus accumbens (NAc), a key brain reward region, has been most studied in animal models of drug addiction, with considerable evidence indicating that ΔFosB promotes reward and motivation and serves as a mechanism of drug sensitization and increased drug self-administration. In more recent years, prolonged induction of ∆FosB has also been observed within NAc in response to chronic administration of certain forms of stress. Increasing evidence indicates that this induction represents a positive, homeostatic adaptation to chronic stress, since overexpression of ∆FosB in this brain region promotes resilience to stress, whereas blockade of its activity promotes stress susceptibility. Chronic administration of several antidepressant medications also induces ∆FosB in the NAc, and this induction is required for the therapeutic-like actions of these drugs in mouse models. Validation of these rodent findings is the demonstration that depressed humans, examined at autopsy, display reduced levels of ∆FosB within the NAc. As a transcription factor, ΔFosB produces this behavioral phenotype by regulating the expression of specific target genes, which are under current investigation. These studies of ΔFosB are providing new insight into the molecular basis of depression and antidepressant action, which is defining a host of new targets for possible therapeutic development.
ΔFosB是转录因子Fos家族的成员。虽然其他家族成员会在一系列急性刺激下迅速但短暂地被诱导产生,但ΔFosB的独特之处在于,由于其异常的蛋白质稳定性,它会在反复刺激下积累。在伏隔核(NAc)这个关键的脑奖赏区域内,ΔFosB的这种长期诱导在药物成瘾的动物模型中得到了最多的研究,有大量证据表明,ΔFosB促进奖赏和动机,并作为药物致敏和增加药物自我给药的一种机制。近年来,在NAc内也观察到了因长期给予某些形式的应激而导致的ΔFosB的长期诱导。越来越多的证据表明,这种诱导代表了对慢性应激的一种积极的稳态适应,因为在这个脑区中ΔFosB的过表达会促进对压力的恢复力,而阻断其活性则会促进压力易感性。几种抗抑郁药物的长期给药也会在NAc中诱导ΔFosB,并且这种诱导是这些药物在小鼠模型中产生类似治疗作用所必需的。对这些啮齿动物研究结果的验证是,对抑郁症患者进行尸检时发现,他们伏隔核内的ΔFosB水平降低。作为一种转录因子,ΔFosB通过调节特定靶基因的表达来产生这种行为表型,目前这些靶基因正在研究中。对ΔFosB的这些研究为抑郁症和抗抑郁作用的分子基础提供了新的见解,这正在为可能的治疗开发确定一系列新的靶点。