路易体痴呆患者亚属扣带皮层多巴胺能变化与抑郁症的存在相关。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Lina Gliaudelytė, Steven P Rushton, Rolando Berlinguer-Palmini, Alan J Thomas, Christopher M Morris
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引用次数: 0

摘要

除了认知波动、视觉幻觉和帕金森等核心临床特征外,路易体痴呆患者还经常经历慢性和衰弱性重度抑郁症。由于缺乏有效的治疗方法,DLB患者的抑郁症治疗受到阻碍,而重度抑郁症(MDD)的标准血清素能药物治疗通常无效。在重度抑郁症中,多巴胺能神经传递功能障碍导致快感缺乏和动机丧失。亚属前扣带皮层(sgACC)在情绪调节和抑郁症状表达中起重要作用,在重度抑郁症中表现出结构、功能和代谢异常。为了评估DLB中多巴胺能和血清素能突触的变化,我们使用高分辨率刺激发射损耗显微镜(STED)以及Western和dot blotting技术研究了DLB供体死后sgACC组织,无论有无抑郁症。STED成像显示,在sgACC的单个多巴胺能末端存在α-synuclein, α-synuclein的存在与抑郁症DLB患者突触体相关蛋白25 kDa (SNAP25)体积增加呈显著正相关。与对照组相比,伴有抑郁症的DLB患者的sgACC中多巴胺能神经支配减少
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dopaminergic changes in the subgenual cingulate cortex in dementia with lewy bodies associates with presence of depression.

In addition to the core clinical features of fluctuating cognition, visual hallucinations, and parkinsonism, individuals with dementia with Lewy bodies (DLB) frequently experience chronic and debilitating major depression. Treatment of depression in DLB is hampered by a lack of available effective therapies and standard serotonergic medication for major depressive disorder (MDD) is typically ineffective. Dysfunction of dopaminergic neurotransmission contributing to anhedonia and loss of motivation has been described in MDD. The subgenual anterior cingulate cortex (sgACC) is important in mood regulation and in the symptomatic expression of depression, displaying structural, functional and metabolic abnormalities in MDD. To assess dopaminergic and serotonergic synaptic changes in DLB, post mortem sgACC tissue from DLB donors with and without depression was investigated using high-resolution stimulated emission depletion (STED) microscopy, as well as Western and dot blotting techniques. STED imaging demonstrated the presence of α-synuclein within individual dopaminergic terminals in the sgACC, α-synuclein presence showing a significant positive correlation with increased synaptosomal associated protein 25 kDa (SNAP25) volumes in depressed DLB cases. A reduction in dopaminergic innervation in the sgACC was observed in DLB cases with depression compared to controls (p < 0.001), but not in non-depressed DLB donors, along with reduced levels of multiple dopaminergic markers and receptors. Limited alterations were observed in serotonergic markers. Our work demonstrates a role for dopaminergic neurotransmission in the aetiology of depression in DLB. Careful and selective targeting of dopaminergic systems in the sgACC may be a therapeutic option for treatment of depression in DLB.

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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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