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Front & Back Matter 正面和背面
Pub Date : 2019-10-01 DOI: 10.1159/000504187
A. Halaris, B. Leonard
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引用次数: 0
Research Domain Criteria: Strengths, Weaknesses, and Potential Alternatives for Future Psychiatric Research 研究领域标准:优势、劣势和未来精神病学研究的潜在选择
Pub Date : 2019-08-13 DOI: 10.1159/000501797
C. Ross, R. Margolis
The Research Domain Criteria (RDoC) paradigm was launched 10 years ago as a superior approach for investigation of mental illness. RDoC conceptualizes normal human behavior, emotion, and cognition as dimensional, with mental illnesses as dimensional extremes. We suggest that RDoC may have value for understanding normal human psychology and some conditions plausibly construed as extremes of normal variation. By contrast, for the most serious of mental illnesses, including dementia, autism, schizophrenia, and bipolar disorder, we argue that RDoC is conceptually flawed. RDoC conflates variation along dimensional axes of normal function with quantitative measurements of disease phenotypes and with the occurrence of diseases in overlapping clusters or spectra. This moves away from the disease model of major mental illness. Further, RDoC imposes a top-down approach to research. We argue that progress in major mental illness research will be more rapid with a bottom-up approach, starting with the discovery of etiological factors, proceeding to investigation of pathogenic pathways, including use of cell and animal models, and leading to a refined nosology and novel, targeted treatments.
研究领域标准(RDoC)范式是10年前作为一种研究精神疾病的优越方法而推出的。RDoC将正常的人类行为、情感和认知概念化为维度,将精神疾病概念化为维度的极端。我们认为,RDoC可能对理解正常的人类心理和一些可能被解释为正常变异的极端情况有价值。相比之下,对于最严重的精神疾病,包括痴呆、自闭症、精神分裂症和双相情感障碍,我们认为RDoC在概念上是有缺陷的。RDoC将正常功能沿维度轴的变化与疾病表型的定量测量以及重叠簇或谱中疾病的发生相结合。这偏离了主要精神疾病的疾病模型。此外,RDoC采用自上而下的方法进行研究。我们认为,如果采用自下而上的方法,从发现病因开始,到研究致病途径,包括使用细胞和动物模型,并导致精细化的分类学和新颖的靶向治疗,重大精神疾病研究的进展将会更快。
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引用次数: 43
Front & Back Matter 正面和背面
Pub Date : 2019-06-01 DOI: 10.1159/000501491
W. Wiersinga, G. Kahaly, V. Blanchette, L. Brandão, V. Breakey, S. Revel-Vilk, W. Byerley, J. Gelernter, T. Petryshen
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引用次数: 0
Regulation and Function of Activity-Dependent Homer in Synaptic Plasticity 活动依赖性Homer在突触可塑性中的调节和功能
Pub Date : 2019-05-23 DOI: 10.1159/000500267
N. Clifton, Simon Trent, K. Thomas, J. Hall
Alterations in synaptic signaling and plasticity occur during the refinement of neural circuits over the course of development and the adult processes of learning and memory. Synaptic plasticity requires the rearrangement of protein complexes in the postsynaptic density (PSD), trafficking of receptors and ion channels and the synthesis of new proteins. Activity-induced short Homer proteins, Homer1a and Ania-3, are recruited to active excitatory synapses, where they act as dominant negative regulators of constitutively expressed, longer Homer isoforms. The expression of Homer1a and Ania-3 initiates critical processes of PSD remodeling, the modulation of glutamate receptor-mediated functions, and the regulation of calcium signaling. Together, available data support the view that Homer1a and Ania-3 are responsible for the selective, transient destabilization of postsynaptic signaling complexes to facilitate plasticity of the excitatory synapse. The interruption of activity-dependent Homer proteins disrupts disease-relevant processes and leads to memory impairments, reflecting their likely contribution to neurological disorders.
突触信号和可塑性的改变发生在发育过程中神经回路的完善和成人的学习和记忆过程中。突触可塑性需要蛋白复合物在突触后密度(PSD)中的重排、受体和离子通道的运输以及新蛋白的合成。活性诱导的短Homer蛋白,Homer1a和Ania-3,被招募到活跃的兴奋性突触,在那里它们作为组成性表达的,较长的Homer亚型的主要负调节因子。Homer1a和Ania-3的表达启动PSD重塑、谷氨酸受体介导的功能调节和钙信号的调控等关键过程。总之,现有的数据支持Homer1a和Ania-3负责突触后信号复合物的选择性,短暂的不稳定,以促进兴奋性突触的可塑性。依赖活动的荷马蛋白的中断破坏了与疾病相关的过程,导致记忆障碍,反映了它们可能对神经系统疾病的贡献。
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引用次数: 45
κ-Opioid Receptor Modulation of GABAergic Inputs onto Ventrolateral Periaqueductal Gray Dopamine Neurons κ-阿片受体对腹外侧导水管周围灰色多巴胺神经元gaba能输入的调节
Pub Date : 2019-05-17 DOI: 10.1159/000496974
Chia Li, T. Kash
The κ-opioid receptor (KOR) system has been implicated in the regulation of many behaviors including pain. While there are numerous studies suggesting KOR regulation of pain being mediated spinally, there have been reports of pain-like behaviors regulated by central KOR signaling. In particular, oxytocin-induced analgesia appears to be mediated by KOR receptors within the ventrolateral periaqueductal gray (vlPAG). We recently found that activation of dopamine (DA) neurons within the vlPAG is antinociceptive. In this study, we sought to determine the impact of KOR signaling on GABAergic inputs onto vlPAG DA neurons, and the mechanism through which KOR impacts these inputs. We found that activation of KOR reduced GABAergic transmission onto vlPAG DA neurons. In addition, our data suggest this effect is mediated presynaptically via the G protein βγ-subunit. They raise the possibility that KOR activation disinhibits vlPAG DA neurons, which could lead to altered regulation of pain-related behaviors.
κ-阿片受体(KOR)系统参与了包括疼痛在内的许多行为的调节。虽然有许多研究表明,KOR对疼痛的调节是通过脊柱介导的,但也有报道称,中枢KOR信号调节了疼痛样行为。特别是,催产素诱导的镇痛似乎是由腹外侧导水管周围灰质(vlPAG)内的KOR受体介导的。我们最近发现,vlPAG内多巴胺(DA)神经元的激活具有抗感受性。在本研究中,我们试图确定KOR信号对gabaergy输入到vlPAG DA神经元的影响,以及KOR影响这些输入的机制。我们发现,激活KOR可减少gaba能在vlPAG DA神经元上的传递。此外,我们的数据表明这种作用是通过G蛋白βγ-亚基在突触前介导的。他们提出了KOR激活解除vlPAG DA神经元抑制的可能性,这可能导致疼痛相关行为的调节改变。
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引用次数: 10
Sex-Specific Effects of Stress on Mood-Related Gene Expression 应激对情绪相关基因表达的性别特异性影响
Pub Date : 2019-04-30 DOI: 10.1159/000499105
K. Barko, W. Paden, Kelly M. Cahill, M. Seney, R. Logan
Women are twice as likely as men to be diagnosed with major depressive disorder (MDD). Recent studies report distinct molecular changes in depressed men and women across mesocorticolimbic brain regions. However, it is unclear which sex-related factors drive distinct MDD-associated pathology. The goal of this study was to use mouse experimental systems to investigate sex-specific mechanisms underlying the distinct molecular profiles of MDD in men and women. We used unpredictable chronic mild stress to induce an elevated anxiety-/depressive-like state and “four core genotypes” (FCG) mice to probe for sex-specific mechanisms. As predicted, based on previous implications in mood, stress impacted the expression of several dopamine-, GABA-, and glutamate-related genes. Some of these effects, specifically in the prefrontal cortex, were genetic sex-specific, with effects in XX mice but not in XY mice. Stress also impacted gene expression differently across the mesocorticolimbic circuit, with increased expression of mood-related genes in the prefrontal cortex and nucleus accumbens, but decreased expression in basolateral amygdala. Our results suggest that females are sensitive to the effects of chronic stress, partly due to their genetic sex, independent of gonadal hormones. Furthermore, these results point to the prefrontal cortex as the node in the mesocorticolimbic circuitry with the strongest female-specific effects.
女性被诊断为重度抑郁症(MDD)的可能性是男性的两倍。最近的研究报告了抑郁症男性和女性中皮质边缘脑区的明显分子变化。然而,目前尚不清楚哪些性别相关因素驱动不同的mdd相关病理。本研究的目的是利用小鼠实验系统来研究男性和女性重度抑郁症不同分子特征背后的性别特异性机制。我们使用不可预测的慢性轻度应激诱导焦虑/抑郁样状态升高,并使用“四核心基因型”(FCG)小鼠来探索性别特异性机制。正如预测的那样,基于先前对情绪的影响,压力影响了几种多巴胺,GABA和谷氨酸相关基因的表达。其中一些影响,特别是在前额叶皮层,是遗传性别特异性的,在XX小鼠中有影响,而在XY小鼠中没有。应激对中皮质边缘回路基因表达的影响也不同,前额叶皮层和伏隔核的情绪相关基因表达增加,而杏仁核基底外侧的表达减少。我们的研究结果表明,女性对慢性压力的影响很敏感,部分原因是由于她们的遗传性别,与性腺激素无关。此外,这些结果表明前额叶皮层是中皮质边缘回路的节点,对女性的特异性影响最大。
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引用次数: 27
Complex Neurological Phenotype in Female Carriers of NHE6 Mutations. NHE6突变女性携带者的复杂神经表型
Pub Date : 2019-04-01 Epub Date: 2019-03-06 DOI: 10.1159/000496341
Matthew F Pescosolido, Brian C Kavanaugh, Nathalie Pochet, Michael Schmidt, Beth A Jerskey, Jeffrey M Rogg, Philip L De Jager, Tracy L Young-Pearse, Judy S Liu, Eric M Morrow

Mutations in NHE6 (also termed SLC9A6) cause the X-linked neurological disorder Christianson syndrome (CS) in males. The purpose of this study was to examine the phenotypic spectrum of female carriers of NHE6 mutations. Twenty female carriers from 9 pedigrees were enrolled, ranging from approximately age 2 to 65. A subset of female carriers was assessed using standardized neuropsychological measures. Also, the association of NHE6 expression with markers of brain age was evaluated using 740 participants in the Religious Orders Study (ROS) and Rush Memory and Aging Project (MAP). A majority, but not all, female carriers demonstrated a deficit in at least one neurocognitive domain (85%). A recognizable neuropsychological profile emerged, revealing impairments in visuospatial function, attention, and executive function. Common neuropsychiatric diagnoses included: intellectual disability/developmental delay (20%), learning difficulties (31%), speech/language delays (30%), and attention-deficit/hyperactivity disorder (20%). Notable neurological diagnoses in aging CS female carriers include corticobasal degeneration and atypical parkinsonism. In postmortem brains from the ROS/MAP dataset of normal and pathological aging, decreased NHE6 expression was correlated with greater tau deposition. Our study provides an examination of the phenotypic range in female carriers of NHE6 mutations. The findings indicate that NHE6-related disease in females represents a new neurogenetic condition.

NHE6(也称为SLC9A6)的突变导致男性x连锁神经系统疾病克里斯蒂安森综合征(CS)。本研究的目的是研究NHE6突变女性携带者的表型谱。来自9个血统的20名女性携带者被纳入研究,年龄从大约2岁到65岁不等。使用标准化的神经心理学测量方法评估女性携带者的子集。此外,在宗教秩序研究(ROS)和Rush记忆与衰老项目(MAP)中,740名参与者评估了NHE6表达与脑年龄标记的关系。大多数,但不是全部,女性携带者表现出至少一个神经认知领域的缺陷(85%)。一个可识别的神经心理学轮廓出现了,揭示了视觉空间功能、注意力和执行功能的损伤。常见的神经精神诊断包括:智力障碍/发育迟缓(20%),学习困难(31%),言语/语言迟缓(30%)和注意力缺陷/多动障碍(20%)。在老年CS女性携带者中值得注意的神经学诊断包括皮质基底变性和非典型帕金森病。在来自正常和病理性衰老的ROS/MAP数据集的死后大脑中,NHE6表达的降低与tau沉积的增加相关。我们的研究提供了在NHE6突变的女性携带者表型范围的检查。研究结果表明,nhe6相关疾病在女性中是一种新的神经遗传疾病。
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引用次数: 9
Electroconvulsive Therapy and Schizophrenia: A Systematic Review. 电休克疗法和精神分裂症:系统综述。
Pub Date : 2019-04-01 Epub Date: 2019-04-02 DOI: 10.1159/000497376
Sana A Ali, Nandita Mathur, Anil K Malhotra, Raphael J Braga

Electroconvulsive therapy (ECT) is a remarkably effective treatment for major depressive disorder, but is less commonly utilized for treatment of psychotic disorders. Recent literature indicates that ECT can be a useful strategy for a wide range of psychotic disorders, including treatment-resistant schizophrenia. The purpose of this review is to examine the extant literature on ECT in schizophrenia with a primary focus on its efficacy, its impact on cognitive function, the role of maintenance ECT, and the potential role of neuroimaging biomarkers to provide more precise ECT treatment strategies. We evaluated the available literature, with a particular focus on prospective, randomized trials. Our review suggests that ECT can be an effective treatment strategy in this severely ill patient population. Studies suggest that while ECT in schizophrenia is a safe treatment modality, the potential for cognitive impairment must always be carefully weighed. The use and investigation of new biomarker strategies for the pharmacological treatment of schizophrenia, and the extension of these approaches to ECT are also discussed.

电痉挛疗法(ECT)是一种非常有效的治疗抑郁症的方法,但很少用于治疗精神障碍。最近的文献表明,电痉挛疗法对包括难治性精神分裂症在内的多种精神疾病是一种有用的治疗策略。本综述的目的是检查现有的关于ECT治疗精神分裂症的文献,主要关注其疗效,对认知功能的影响,维持ECT的作用,以及神经成像生物标志物的潜在作用,以提供更精确的ECT治疗策略。我们评估了现有文献,特别关注前瞻性随机试验。我们的综述表明,电痉挛疗法是治疗这类重症患者的有效方法。研究表明,虽然ECT治疗精神分裂症是一种安全的治疗方式,但必须始终仔细权衡其对认知障碍的潜在影响。本文还讨论了精神分裂症药物治疗中新的生物标志物策略的使用和研究,以及这些方法在电痉挛疗法中的推广。
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引用次数: 41
Front & Back Matter 正面和背面
Pub Date : 2019-04-01 DOI: 10.1159/000500647
W. Wiersinga, G. Kahaly, V. Blanchette, L. Brandão, V. Breakey, S. Revel-Vilk, W. Byerley, J. Gelernter, T. Petryshen
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引用次数: 0
Entrainment of Circadian Rhythms to Temperature Reveals Amplitude Deficits in Fibroblasts from Patients with Bipolar Disorder and Possible Links to Calcium Channels. 昼夜节律对温度的影响揭示了双相情感障碍患者成纤维细胞的振幅缺陷,并可能与钙通道有关。
Pub Date : 2019-04-01 Epub Date: 2019-04-04 DOI: 10.1159/000497354
Victoria Nudell, Heather Wei, Caroline Nievergelt, Adam X Maihofer, Paul Shilling, Martin Alda, Wade H Berrettini, Kristen J Brennand, Joseph R Calabrese, William H Coryell, Jonathan M Covault, Mark A Frye, Fred Gage, Elliot Gershon, Melvin G McInnis, John I Nurnberger, Ketil J Oedegaard, Tatyana Shekhtman, Peter P Zandi, John R Kelsoe, Michael J McCarthy

Bipolar disorder (BD) is characterized by recurrent mood episodes, and circadian rhythm disturbances. Past studies have identified calcium channel genes as risk loci for BD. CACNA1C encodes an L-type calcium channel (LTCC) involved in the entrainment of circadian rhythms to light. Another calcium channel, i.e., the ryanodine receptor (RYR), is involved in -circadian phase delays. It is unknown whether variants in CACNA1C or other calcium channels contribute to the circadian phenotype in BD. We hypothesized that, by using temperature cycles, we could model circadian entrainment in fibroblasts from BD patients and controls to interrogate the circadian functions of LTCCs. Using Per2-luc, a bioluminescent reporter, we verified that cells entrain to temperature rhythms in vitro. Under constant temperature conditions, the LTCC antagonist verapamil shortened the circadian period, and the RYR antagonist dantrolene lengthened the period. However, neither drug affected temperature entrainment. Fibroblasts from BD patients and controls also entrained to temperature. In cells from BD patients, the rhythm amplitude was lower under entrained, but not constant, conditions. Temperature entrainment was otherwise similar between BD and control cells. However, the CACNA1C genotype among BD cells predicted the degree to which cells entrained. We conclude that assessment of rhythms under entrained conditions reveals additional rhythm abnormalities in BD that are not observable under constant temperature conditions.

双相情感障碍(BD)以反复发作的情绪发作和昼夜节律紊乱为特征。过去的研究已经确定钙通道基因是BD的危险位点。CACNA1C编码l型钙通道(LTCC),参与昼夜节律对光的影响。另一种钙通道,即ryanodine受体(RYR),参与-昼夜节律期延迟。目前尚不清楚CACNA1C或其他钙通道的变异是否与BD的昼夜节律表型有关。我们假设,通过使用温度周期,我们可以模拟BD患者和对照组成纤维细胞的昼夜节律携带,以询问ltcc的昼夜节律功能。利用Per2-luc,一种生物发光报告物,我们证实了细胞在体外受温度节律的影响。在恒温条件下,LTCC拮抗剂维拉帕米缩短了昼夜节律周期,而RYR拮抗剂丹曲林延长了昼夜节律周期。然而,两种药物都不影响温度夹带。BD患者和对照组的成纤维细胞也随温度变化。在BD患者的细胞中,节律振幅在携带条件下较低,但不是恒定条件。在其他方面,BD细胞和对照细胞之间的温度夹带相似。然而,BD细胞中的CACNA1C基因型预测了细胞携带的程度。我们的结论是,在夹带条件下的节律评估揭示了在恒温条件下无法观察到的BD的额外节律异常。
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引用次数: 7
期刊
Molecular Neuropsychiatry
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