Mindscape Collective is now The Consciousness Library. Same library, new name. You may need to sign in again. About the change
Skip to content

Peter C. T. Hawkins

2 papers in the library · 35 citations · publishing 2020-2023

Papers

Preliminary evidence that ketamine alters anterior cingulate resting-state functional connectivity in depressed individuals

Translational Psychiatry December 3, 2023 Laith Alexander, Peter C. T. Hawkins, Jennifer W. Evans et al. 26 citations

Ketamine's antidepressant effects involve changes in brain connectivity that depend on which part of the anterior cingulate cortex (ACC) is examined. In a double-blind, placebo-controlled crossover trial, patients with treatment-resistant depression and healthy volunteers received intravenous ketamine or placebo. Two days later, resting-state functional connectivity between ACC subregions and other brain areas differed between groups. Changes in perigenual ACC connectivity to the insula correlated with improved depression scores. Subgenual ACC connectivity was most altered by ketamine compared to placebo, and changes in its connectivity to other ACC subregions and the ventral striatum correlated with reduced anhedonia. Accurate ACC segmentation is needed to understand ketamine's effects.

Ketamine Modulates the Neural Correlates of Reward Processing in Unmedicated Patients in Remission from Depression

medRxiv Preprint Server December 7, 2020 Vasileia Kotoula, Argyris Stringaris, Nuria Mackes et al. 9 citations preprint

Ketamine, an antidepressant, can alter activity in brain reward areas within two hours of a single infusion, even in people who are not currently depressed. In a study of 37 remitted depression patients, ketamine increased brain responses in the nucleus accumbens and putamen during anticipation and receipt of small rewards, and the level of a ketamine metabolite (2R,6R)-HNK correlated with activation in the ventral tegmental area. These changes occurred without any changes in mood symptoms, suggesting ketamine may improve anhedonia by directly modulating how the brain processes reward feedback.