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本文引用的文献

1
Executive Function Deficits in Daily Life Prospectively Predict Increases in Depressive Symptoms.日常生活中的执行功能缺陷可前瞻性预测抑郁症状的增加。
Cognit Ther Res. 2014 Dec;38(6):612-620. doi: 10.1007/s10608-014-9629-5. Epub 2014 Aug 6.
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Transgenic mouse models for studying adult neurogenesis.用于研究成体神经发生的转基因小鼠模型。
Front Biol (Beijing). 2016 Jun;11(3):151-167. doi: 10.1007/s11515-016-1405-3. Epub 2016 Jun 28.
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PET imaging of neurogenic activity in the adult brain: Toward in vivo imaging of human neurogenesis.成人大脑中神经源性活动的正电子发射断层扫描(PET)成像:迈向人类神经发生的活体成像。
Neurogenesis (Austin). 2017 Feb 6;4(1):e1281861. doi: 10.1080/23262133.2017.1281861. eCollection 2017.
4
Nasal neuron PET imaging quantifies neuron generation and degeneration.鼻神经元PET成像可量化神经元的生成与退化。
J Clin Invest. 2017 Feb 1;127(2):681-694. doi: 10.1172/JCI89162. Epub 2017 Jan 23.
5
Re-evaluating the link between neuropsychiatric disorders and dysregulated adult neurogenesis.重新评估神经精神疾病与成人神经发生失调之间的联系。
Nat Med. 2016 Nov;22(11):1239-1247. doi: 10.1038/nm.4218. Epub 2016 Oct 26.
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Synaptic plasticity and depression: new insights from stress and rapid-acting antidepressants.突触可塑性与抑郁症:应激和速效抗抑郁药带来的新见解。
Nat Med. 2016 Mar;22(3):238-49. doi: 10.1038/nm.4050.
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Neurogenesis-mediated forgetting minimizes proactive interference.神经发生介导的遗忘可将前摄干扰降至最低。
Nat Commun. 2016 Feb 26;7:10838. doi: 10.1038/ncomms10838.
8
Effect of electroconvulsive seizures on cognitive flexibility.电惊厥发作对认知灵活性的影响。
Hippocampus. 2016 Jul;26(7):899-910. doi: 10.1002/hipo.22573. Epub 2016 Mar 7.
9
Mice lacking the PSD-95-interacting E3 ligase, Dorfin/Rnf19a, display reduced adult neurogenesis, enhanced long-term potentiation, and impaired contextual fear conditioning.缺乏与PSD-95相互作用的E3连接酶Dorfin/Rnf19a的小鼠表现出成年神经发生减少、长时程增强增强和情境恐惧条件反射受损。
Sci Rep. 2015 Nov 10;5:16410. doi: 10.1038/srep16410.
10
Regulation of Adult Neurogenesis and Plasticity by (Early) Stress, Glucocorticoids, and Inflammation.(早期)应激、糖皮质激素和炎症对成体神经发生及可塑性的调节
Cold Spring Harb Perspect Biol. 2015 Sep 1;7(9):a021303. doi: 10.1101/cshperspect.a021303.

模式分离:重度抑郁症中海马体成年神经发生受损的潜在标志物。

Pattern Separation: A Potential Marker of Impaired Hippocampal Adult Neurogenesis in Major Depressive Disorder.

作者信息

Gandy Kellen, Kim Sohye, Sharp Carla, Dindo Lilian, Maletic-Savatic Mirjana, Calarge Chadi

机构信息

Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX, United States.

Department of Obstetrics and Gynecology, Baylor College of Medicine and Center for Reproductive Psychiatry, Pavilion for Women, Texas Children's Hospital, Houston, TX, United States.

出版信息

Front Neurosci. 2017 Oct 26;11:571. doi: 10.3389/fnins.2017.00571. eCollection 2017.

DOI:10.3389/fnins.2017.00571
PMID:29123464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5662616/
Abstract

Adult neurogenesis involves the generation of new neurons, particularly in the dentate gyrus of the hippocampus. Decreased hippocampal neurogenesis has been implicated in both animal models of depression and in patients with major depressive disorder (MDD), despite some inconsistency in the literature. Here, we build upon current models to generate a new testable hypothesis, linking impaired neurogenesis to downstream psychological outcomes commonly observed in MDD. We contend that disruption in adult neurogenesis impairs pattern separation, a hippocampus-dependent function requiring the careful discrimination and storage of highly similar, but not identical, sensory inputs. This, in turn, can affect downstream processing and response selection, of relevance to emotional wellbeing. Specifically, disrupted pattern separation leads to misperceived stimuli (i.e., stimulus confusion), triggering the selection and deployment of established responses inappropriate for the actual stimuli. We speculate that this may be akin to activation of automatic thoughts, described in the Cognitive Behavior Theory of MDD. Similarly, this impaired ability to discriminate information at a fundamental sensory processing level (e.g., impaired pattern separation) could underlie impaired psychological flexibility, a core component of Acceptance and Commitment Therapy of MDD. We propose that research is needed to test this model by examining the relationship between cognitive functioning (e.g., pattern separation ability), psychological processes (e.g., perseveration and psychological inflexibility), and neurogenesis, taking advantage of emerging magnetic resonance spectroscopy-based imaging that measures neurogenesis .

摘要

成体神经发生涉及新神经元的生成,尤其是在海马体的齿状回中。尽管文献中存在一些不一致之处,但海马体神经发生减少已在抑郁症动物模型和重度抑郁症(MDD)患者中得到证实。在此,我们在现有模型的基础上提出一个新的可检验假设,将神经发生受损与MDD中常见的下游心理结果联系起来。我们认为,成体神经发生的破坏会损害模式分离,这是一种依赖海马体的功能,需要对高度相似但不完全相同的感觉输入进行仔细辨别和存储。反过来,这会影响与情绪健康相关的下游处理和反应选择。具体而言,模式分离受到破坏会导致对刺激的错误感知(即刺激混淆),从而触发对实际刺激不适当的既定反应的选择和运用。我们推测,这可能类似于MDD认知行为理论中所描述的自动思维的激活。同样,在基本感觉处理水平上辨别信息的能力受损(例如模式分离受损)可能是心理灵活性受损的基础,而心理灵活性是MDD接受与承诺疗法的核心组成部分。我们建议需要开展研究,利用新兴的基于磁共振波谱的成像技术来测量神经发生,通过检查认知功能(如模式分离能力)、心理过程(如固执和心理僵化)与神经发生之间的关系来检验该模型。