条件刺激触发记忆恢复-消退在甲基苯丙胺使用障碍患者中的作用。

IF 6.2 1区 医学 Q1 PSYCHIATRY
Jing-Li Yue, Ru-Jia Wang, Si-Jing Chen, Xiao Lin, Qing Fang, Xiao-Jie Guo, Ye-Kun Sun, Kai Yuan, Yan-Ping Bao, Jie Shi, Yan-Xue Xue, Ping Wu, Lin Lu
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引用次数: 0

摘要

甲基苯丙胺是一种被广泛滥用的兴奋剂,它会影响中枢神经系统。持续的不适应条件刺激(CS,药物线索)-药物联想记忆是诱发复发的主要因素。干扰这些记忆的重新巩固可能有助于破坏和改变这些不适应的cs -药物关联,潜在地减少它们对寻求药物行为的影响。本研究探索了cs触发的记忆恢复-消失对冰毒渴求的影响,可能为成瘾提供一种新的治疗策略。这是一项涉及冰毒使用障碍(MUD)个体的单中心、随机、对照试验。参与者在连续的一天(第2天和第3天)完成了三种干预措施中的一种:cs触发的记忆检索随后在间隔10分钟后消失,cs触发的记忆检索随后在间隔6小时后消失,或在没有事先检索的情况下消失。在基线(第1天)、干预后(第4天)和两个随访时间点(第34天和第184天)测量自我报告线索诱导的甲基苯丙胺渴望、唾液皮质醇和交感神经反应,以线索诱导的渴望和唾液皮质醇作为主要结局。共98例MUD患者,平均年龄28.15±6.31岁。经过2天的干预,线索诱导的冰毒渴求(时间×线索交互作用:F(1,94) = 60.02, p (2,94) = 14.32, p (2,94) = 24.28, p (2,90) = 9.51, p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of conditioned stimuli-triggered memory retrieval-extinction in patients with methamphetamine use disorder.

Effect of conditioned stimuli-triggered memory retrieval-extinction in patients with methamphetamine use disorder.

Effect of conditioned stimuli-triggered memory retrieval-extinction in patients with methamphetamine use disorder.

Effect of conditioned stimuli-triggered memory retrieval-extinction in patients with methamphetamine use disorder.

Methamphetamine (METH) is a widely abused stimulant that affects the central nervous system. The persistent maladaptive conditioned stimuli (CS, drug cues)-drug associative memories represent a primary factor precipitating relapse. Interfering with the reconsolidation of these memories may help disrupt and modify these maladaptive CS-drug associations, potentially reducing their influence on drug-seeking behavior. The present study explored the effect of CS-triggered memory retrieval-extinction on METH craving, potentially offering a new treatment strategy for addiction. This was a single-center, randomized, controlled trial involving individuals with METH use disorder (MUD). Participants completed one of three interventions on consecutive days (days 2 and 3): CS-triggered memory retrieval followed by extinction after a 10-min interval, CS-triggered memory retrieval followed by extinction after a 6-h interval, or extinction without prior retrieval. Self-report cue-induced craving for METH, salivary cortisol and sympathetic responses were measured at baseline (day 1), post intervention (day 4) and two follow-up timepoints (days 34 and 184), with cue-induced craving and salivary cortisol as primary outcomes. Ninety-eight MUD individuals (mean age 28.15 ± 6.31) were analyzed. After two-day's interventions, cue-induced METH craving (time × cue interaction: F(1,94) = 60.02, p < 0.001) reduced in all groups. Results from follow-up data indicated, when the extinction was performed 10 min, but not 6 h after memory retrieval or no retrieval, the intervention decreased experimental cue-induced METH craving (intervention × time × cue: F(2,94) = 14.32, p < 0.001; intervention: F(2,94) = 24.28, p < 0.001) and saliva cortisol increases (F(2,90) = 9.51, p < 0.001), with effects lasting up to 6-month follow-up. The results revealed a substantial reduction in cue-elicited craving and saliva cortisol in the retrieval-10 min-extinction group over the 6-month follow-up. These findings provide compelling evidence that a brief reconsolidation-based intervention can effectively diminish METH-related craving and cortisol levels, underscoring its potential as a supportive measure in METH treatment. Salivary cortisol is a readily accessible and sensitive biomarker for evaluating intervention effects.

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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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