WEAKENED ROLE OF VENTROMEDIAL AND DORSOLATERAL PREFRONTAL CORTEX IN REGULATING AMYGDALA ACTIVITY IN LATE-LIFE DEPRESSION – A DYNAMIC CAUSAL MODELLING STUDY ON RESTING STATE FMRI

2020 ◽  
Vol 28 (4) ◽  
pp. S135
Author(s):  
Lihong Wang ◽  
Lihong Wang ◽  
Kevin Manning ◽  
David Steffens
2011 ◽  
Vol 193 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Cheng-Chen Chang ◽  
Shun-Chieh Yu ◽  
Douglas R. McQuoid ◽  
Denise F. Messer ◽  
Warren D. Taylor ◽  
...  

2021 ◽  
pp. 1-15
Author(s):  
Kamin Kim ◽  
Matthew S. Sherwood ◽  
Lindsey K. McIntire ◽  
Andy R. McKinley ◽  
Charan Ranganath

Abstract Studies have shown that transcranial direct current stimulation increases neuronal excitability of the targeted region and general connectivity of relevant functional networks. However, relatively little is understood on how the stimulation affects the connectivity relationship of the target with regions across the network structure of the brain. Here, we investigated the effects of transcranial direct current stimulation on the functional connectivity of the targeted region using resting-state fMRI scans of the human brain. Anodal direct current stimulation was applied to the left dorsolateral prefrontal cortex (lDLPFC; cathode on the right bicep), which belongs to the frontoparietal control network (FPCN) and is commonly targeted for neuromodulation of various cognitive functions including short-term memory, long-term memory, and cognitive control. lDLPFC's connectivity characteristics were quantified as graph theory measures, from the resting-state fMRI scans obtained prior to and following the stimulation. Critically, we tested pre- to poststimulation changes of the lDLPFC connectivity metrics following an active versus sham stimulation. We found that the stimulation had two distinct effects on the connectivity of lDLPFC: for Brodmann's area (BA) 9, it increased the functional connectivity between BA 9 and other nodes within the FPCN; for BA 46, net connectivity strength was not altered within FPCN, but connectivity distribution across networks (participation coefficient) was decreased. These findings provide insights that the behavioral changes as the functional consequences of stimulation may come about because of the increased role of lDLPFC in the FPCN.


2009 ◽  
Vol 195 (2) ◽  
pp. 163-169 ◽  
Author(s):  
Ahmad Khundakar ◽  
Christopher Morris ◽  
Arthur Oakley ◽  
William McMeekin ◽  
Alan J. Thomas

BackgroundLate-life depression has been associated with cerebrovascular disease and especially with ischaemic white matter hyperintensities on magnetic resonance imaging. Neuroimaging and morphometric studies have identified abnormalities in the dorsolateral prefrontal cortex.AimsTo examine glial and neuronal density and neuronal volume in the dorsolateral prefrontal cortex in late-life major depression.MethodWe used the disector and nucleator methods to estimate neuronal density and volume and glial density of cells in the dorsolateral prefrontal cortex in a post-mortem study of 17 individuals with late-life major depression and 10 age-matched controls.ResultsWe found a reduction in the volume of pyramidal neurones in the whole cortex, which was also present in layer 3 and more markedly in layer 5. There were no comparable changes in non-pyramidal neurones and no glial differences.ConclusionsOverall, we found a decrease in pyramidal neuronal size in the dorsolateral prefrontal cortex in late-life depression.


2002 ◽  
Vol 18 (1) ◽  
pp. 7-13 ◽  
Author(s):  
Alan J. Thomas ◽  
Robert Perry ◽  
Rajesh N. Kalaria ◽  
Arthur Oakley ◽  
William McMeekin ◽  
...  

2004 ◽  
Vol 161 (7) ◽  
pp. 1293-1296 ◽  
Author(s):  
Warren D. Taylor ◽  
James R. MacFall ◽  
Martha E. Payne ◽  
Douglas R. McQuoid ◽  
James M. Provenzale ◽  
...  

2010 ◽  
Vol 23 (4) ◽  
pp. 644-653 ◽  
Author(s):  
Ahmad Khundakar ◽  
Christopher Morris ◽  
Alan J. Thomas

ABSTRACTBackground: The “vascular depression” hypothesis has sought to explain differences in etiology between early and late life depression, and has been reinforced by recent imaging and morphometric studies. Gamma-aminobutyric acid (GABA) is thought to play a major role in the neurobiology of depression. However, it is unclear whether there is an effect on GABA neuronal subpopulations in an elderly depressed cohort. This study therefore examined immunohistochemically two calcium-binding proteins, calretinin and parvalbumin, which have been demonstrated to bind to two distinct GABAergic interneuron subpopulations, within the dorsolateral prefrontal cortex (DLPFC) of elderly depressed patients, against age-matched controls.Methods: Post-mortem tissue was obtained from nine controls and 11 depressed patients for the parvalbumin study and seven controls and 14 depressed patients in the calretinin study, and the mean percentage per area of immunohistochemical staining of the two antibodies was measured in individual layers and across the whole of the DLPFC.Results: The study found a reduction in parvalbumin immunostaining in layer 6 (p = 0.05) of the DLFPC in elderly depressed patients. However, no significant changes were found in parvalbumin or calretinin immunostaining in the any other layer of the DLPFC in elderly depressed patients.Conclusion: The study does not suggest any change in GABA interneuron subpopulations, though significant reductions in layer 6 may represent subtle disturbance in GABA parvalbumin-expressing interneuron and glumatatergic pyramidal projection neuron regulation in late-life depression.


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