scholarly journals The Role of Intrinsic Brain Functional Connectivity in Vulnerability and Resilience to Bipolar Disorder

2017 ◽  
Vol 174 (12) ◽  
pp. 1214-1222 ◽  
Author(s):  
Gaelle E. Doucet ◽  
Danielle S. Bassett ◽  
Nailin Yao ◽  
David C. Glahn ◽  
Sophia Frangou
2020 ◽  
Vol 14 ◽  
Author(s):  
Yen-Ling Chen ◽  
Pei-Chi Tu ◽  
Tzu-Hsuan Huang ◽  
Ya-Mei Bai ◽  
Tung-Ping Su ◽  
...  

Author(s):  
Yicheng Long ◽  
Zhening Liu ◽  
Calais Kin-yuen Chan ◽  
Guowei Wu ◽  
Zhimin Xue ◽  
...  

AbstractSchizophrenia and bipolar disorder share some common clinical features and are both characterized by aberrant resting-state functional connectivity (FC). However, little is known about the common and specific aberrant features of the dynamic FC patterns in these two disorders. In this study, we explored the differences in dynamic FC among schizophrenia patients (n = 66), type I bipolar disorder patients (n = 53) and healthy controls (n = 66), by comparing temporal variabilities of FC patterns involved in specific brain regions and large-scale brain networks. Compared with healthy controls, both patient groups showed significantly increased regional FC variabilities in subcortical areas including the thalamus and basal ganglia, as well as increased inter-network FC variability between the thalamus and sensorimotor areas. Specifically, more widespread changes were found in the schizophrenia group, involving increased FC variabilities in sensorimotor, visual, attention, limbic and subcortical areas at both regional and network levels, as well as decreased regional FC variabilities in the default-mode areas. The observed alterations shared by schizophrenia and bipolar disorder may help to explain their overlapped clinical features; meanwhile, the schizophrenia-specific abnormalities in a wider range may support that schizophrenia is associated with more severe functional brain deficits than bipolar disorder.


2021 ◽  
Author(s):  
Manfred Klöbl ◽  
René Seiger ◽  
Thomas Vanicek ◽  
Patricia Handschuh ◽  
Murray Bruce Reed ◽  
...  

AbstractLearning-induced neuroplastic changes, further modulated by content and setting, are mirrored in brain functional connectivity. Animal models emphasized the crucial role of serotonin in neuroplasticity particularly for emotional relearning, but comparable studies in humans are scarce. Assessing the translation of learning effects from animals to humans, 99 healthy subjects underwent six weeks of emotional or semantic learning and subsequent relearning and three resting-state acquisitions for functional connectivity estimation. During relearning, subjects received either a daily dose of the selective serotonin reuptake inhibitor escitalopram or placebo. The influence of escitalopram on functional connectivity was connection- and learning content-dependent, with potentiation of decreases during emotional and increases during semantic learning. The directedness of these effects indicates serotonergic modulation of emotional feedback routes. These results demonstrate that escitalopram intake during relearning facilitates content-dependent network adaptations and support the conclusion that enhanced neuroplasticity might be the major underlying mechanism in psychiatric therapies.


2021 ◽  
Vol 89 (9) ◽  
pp. S296
Author(s):  
Anjali Sankar ◽  
Dustin Scheinost ◽  
Danielle Goldman ◽  
Rebecca Drachman ◽  
Lejla Colic ◽  
...  

2021 ◽  
Author(s):  
Senthilkumar Deivasigamani ◽  
Mariya Timotey Miteva ◽  
Silvia Natale ◽  
Daniel Gutierrez-Barragan ◽  
Bernadette Basilico ◽  
...  

Complement signaling is thought to serve as an opsonization signal to promote the phagocytosis of synapses by microglia. However, while its role in synaptic remodeling has been demonstrated in the retino-thalamic system, it remains unclear whether complement signaling mediates synaptic pruning in the brain more generally. Here we show that mice lacking the complement 3 receptor (C3r), the major microglia complement receptor, fail to show a deficit in either synaptic pruning or axon elimination in the developing mouse cortex. Instead, mice lacking C3r show a deficit in the perinatal elimination of neurons, both in the retina as well as in the cortex, a deficit that is associated with increased cortical thickness and enhanced functional connectivity in these regions in adulthood. These data demonstrate a preferential role for complement in promoting neuronal elimination in the developing brain and argue for a reconsideration of the role of complement in synaptic pruning.


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