重新评估我们的戒毒重点:情绪失调是导致复吸的关键因素。

IF 5.8 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2024-11-09 DOI:10.1038/s41398-024-03159-5
Lexi J Hand, Louise M Paterson, Anne R Lingford-Hughes
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引用次数: 0

摘要

大多数成瘾研究都侧重于与奖赏和冲动相关的神经回路。然而,成瘾周期中的戒断/负面影响阶段的影响却在某种程度上被忽视了,尽管它在临床上很常见。这一阶段对重复吸毒和复吸的负强化起着至关重要的作用,但人们对其神经基础却知之甚少。人们对药物依赖中的负性情绪处理是如何失调的尚不完全清楚,不同类型的药物可能表现出不同的负性情绪处理。反过来,消极情绪处理所涉及的区域也可能表现出不同的失调模式。了解不同物质导致的消极状态所涉及的神经回路有何不同,可能有助于找到新的治疗目标。在对有关药物依赖中负面情绪处理的研究进行了全面的文献检索后,我们认为定量的方法并不合适。相反,我们采用了一种叙事方法来探索神经对涉及酒精、可卡因、阿片类药物和大麻依赖的情绪处理任务的反应。结果发现,杏仁核、脑岛、前扣带回和内侧前额叶皮层等区域出现了失调。然而,酒精、可卡因、阿片类药物和大麻依赖的反应模式各不相同。酒精依赖症患者的大脑激活对负面情绪刺激和情绪面孔的反应普遍减弱,而可卡因依赖症患者的大脑激活则相反地增强。在阿片类药物依赖中,杏仁核一直受到牵连,而在大麻依赖中,岛叶、前扣带回和内侧前额叶皮层受到牵连。然而,这些研究之间存在很大差异,只有极少数研究对阿片类药物和大麻依赖进行了调查。这些发现表明,情绪失调因药物依赖类型而异。然而,研究结果的差异和研究的缺乏凸显了在这一领域开展更多研究的必要性。进一步描述药物依赖中情绪失调的特征将有助于确定治疗目标。更有针对性的治疗方法可以调节消极情绪处理,从而有助于预防复发,从而大大改善治疗效果。
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Re-evaluating our focus in addiction: emotional dysregulation is a critical driver of relapse to drug use.

Most addiction research has focused on reward- and impulsivity-related neurocircuitry. However, the impact of the withdrawal/negative affect stage in the addiction cycle has been somewhat overlooked, despite it being commonly evident in the clinic. This stage crucially drives negative reinforcement of repeated drug use and relapse, yet less is known about its neural underpinnings. How negative emotional processing is dysregulated in substance dependence is incompletely understood and may manifest differentially across the types of substances. In turn, the regions involved in negative emotional processing may show different patterns of dysregulation. Understanding how neurocircuitry involved in negative states differs across various substances may help inform new targets for treatments. Following a comprehensive literature search of studies examining negative emotional processing in substance dependence, a quantitative approach was deemed inappropriate. Instead, we employed a narrative approach to exploring neural responses to tasks involving emotional processing in alcohol, cocaine, opioid and cannabis dependence. Regions that were found to be dysregulated included the amygdala, insula, anterior cingulate, and medial prefrontal cortex. However, patterns of reactivity differed across alcohol, cocaine, opioid and cannabis dependence. Brain activation in alcohol dependence broadly appeared blunted in response to negative affective stimuli and emotional faces, whilst conversely appeared heightened in cocaine dependence. In opioid dependence, the amygdala was consistently implicated, whilst the insula, anterior cingulate, and medial prefrontal cortex were implicated in cannabis dependence. However, there was wide variability amongst the studies, with very few studies investigating opioid and cannabis dependence. These findings suggest emotional dysregulation varies according to the type of substance dependence. However, the variability in findings and lack of studies highlights the need for more research in this area. Further characterisation of emotional dysregulation in substance dependence will enable identification of treatment targets. More targeted treatments that modulate negative emotional processing could substantially improve outcomes by aiding relapse prevention.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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