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Effects of post-session administration of methylene blue on fear extinction and contextual memory in adults with claustrophobia

机译:亚甲基蓝蓝色施用对幽闭症的恐惧灭绝与语境记忆的影响

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Objective: Preclinical studies have shown that low-dose methylene blue increases mitochondrial cytochrome oxidase activity in the brain and improves memory retention after learning tasks, including fear extinction. The authors report on the first controlled experiment to examine the memory-enhancing effects of posttraining methylene blue administration on retention of fear extinction and contextual memory following fear extinction training. Method: Adult participants displaying marked claustrophobic fear were randomly assigned to double-blind administration of 260 mg of methylene blue (N=23) or administration of placebo (N=19) immediately following six 5-minute extinction trials in an enclosed chamber. Retesting occurred 1 month later to assess fear renewal as indexed by peak fear during exposure to a nontraining chamber, with the prediction that the effects of methylene blue would vary as a function of fear reduction achieved during extinction training. Incidental contextual memory was assessed 1 and 30 days after training to assess the cognitive-enhancing effects of methylene blue independent of its effects on fear attenuation. Results: Consistent with predictions, participants displaying low end fear posttraining showed significantly less fear at the 1-month follow-up if they received methylene blue posttraining compared with placebo. In contrast, participants displaying moderate to high levels of posttraining fear tended to fare worse at the follow-up if they received methylene blue posttraining. Methylene blue's enhancement of contextual memory was unrelated to initial or posttraining claustrophobic fear. Conclusions: Methylene blue enhances memory and the retention of fear extinction when administered after a successful exposuresession but may have a deleterious effect on extinction when administered after an unsuccessful exposure session.
机译:目的:临床前研究表明,低剂量亚甲基蓝增加了大脑中的线粒体细胞色素氧化酶活性,并在学习任务之后提高了记忆保留,包括恐惧灭绝。作者报告了第一个受控实验,以检查预订亚甲基蓝色管理的内存增强效果是否保留恐惧灭绝后的恐惧灭绝和情境记忆之后。方法:随机分配显示标记的幽闭恐惧的成人参与者在封闭室中的六个5分钟消失试验后立即分配给260mg亚甲基蓝(n = 23)或施用安慰剂(n = 19)。重新测试发生在1个月后,以评估在暴露于非浮选室内的峰值恐惧的峰值恐惧评估恐惧更新,预测亚甲基蓝的效果在消灭训练期间达到恐惧减少的函数变化。训练后1和30天评估偶然的上下文记忆,以评估亚甲蓝独立于其对恐惧衰减的影响的认知增强效果。结果:与预测一致,展示低端恐惧的参与者在与安慰剂相比接受亚甲基蓝色后续后,在1个月的随访中表现出显着较少的恐惧。相比之下,如果他们在接受亚甲基蓝色后接受后,参与者展示中度至高水平的过度接触恐惧趋势往往在随访时更糟糕。亚甲基蓝色的上下文记忆的增强与初始或后期幽闭恐惧症无关。结论:亚甲基蓝增强内存,在成功曝光后给药时恐惧灭绝的保留率,但在不成功的曝光会议后给药时可能对灭绝有害影响。

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