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Incapacity to control emotion in major depression may arise from disrupted white matter integrity and OFC OFC ‐amygdala inhibition

机译:在严重的白质完整性和OFC-amygdala抑制中可能出现在重大抑郁症中的情绪的干扰

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Summary Background Disturbances in emotion regulation are the hallmarks of major depressive disorder (MDD). The incapacity to control negative emotion in patients has been associated with abnormal hyperactivation of the limbic system and hypoactivation of the frontal cortex. The amygdala and orbital frontal cortex (OFC) are two critical regions of the emotion regulation neural systems. Methods This study investigated the anatomical basis of abnormal emotion regulation by tracking the fiber tracts connecting the amygdala and OFC. In addition, using dynamic casual modeling on resting‐state fMRI data of 20 MDD patients and equivalent controls, we investigated the exact neural mechanism through which abnormal communications between these two nodes were mediated in MDD. Key Results The results revealed disrupted white matter integrity of fiber tracts in MDD, suggesting that functional abnormalities were accompanied by underlying anatomical basis. We also detected a failure of inhibition of the OFC on the activity of the amygdala in MDD, suggesting dysconnectivity was mediated through “top‐down” influences from the frontal cortex to the amygdala. Following 8 weeks of antidepressant treatment, the patients showed significant clinical improvement and normalization of the abnormal OFC‐amygdala structural and effective connectivity in the left hemisphere. Conclusions & Inferences Our findings suggest that pathways connecting these two nodes may be core targets of the antidepressant treatment. In particular, it raised the intriguing question: Does the reversal of structural markers of connectivity reflect a response to antidepressant medication or activity‐dependent myelination following a therapeutic restoration of effective connectivity?
机译:总结情绪调节中的背景是主要抑郁症(MDD)的标志。控制患者负面情绪的干扰已经与肢体系统的异常激活和额叶皮质的低动激活有关。 Amygdala和轨道正面皮质(OFC)是情绪调节神经系统的两个关键区域。方法本研究通过跟踪连接Amygdala和OFC的纤维束来调查异常情绪调节的解剖学依据。此外,在休息状态下使用动态休闲建模20 MDD患者和等效控制,我们调查了这些两个节点之间的异常通信的确切神经机制,在MDD中介导。关键结果结果显示,MDD中纤维纤维的白质完整性突破,表明功能异常伴随着根本解剖学。我们还检测到OFC对MDD中杏仁醛的活性的抑制失败,表明脱孔奈基通过“自上而下”介导来自颅骨的“自上而下”。在8周的抗抑郁治疗后,患者显示出显着的临床改善和左半球结构和有效连通性的异常的临床改善和标准化。结论&推论我们的研究结果表明,连接这两个节点的途径可以是抗抑郁治疗的核心靶标。特别是,它提出了有趣问题:连接性结构标志物的逆转反映了在有效连接的治疗恢复后对抗抑郁药物或活性依赖性髓鞘产生的反应吗?

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