Gandy Kellen, Kim Sohye, Sharp Carla, Dindo Lilian, Maletic-Savatic Mirjana, Calarge Chadi
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.
Front Neurosci. 2017 Oct 26;11:571. doi: 10.3389/fnins.2017.00571. eCollection 2017.
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 .
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。