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Kantaro Nishigori

Sumitomo Pharma Co., Ltd., Tokyo, Japan.

2 papers in the library · 1 citation · publishing 2025-2026

Papers

Ketamine effects on resting state functional brain connectivity in major depressive disorder patients: a hypothesis-driven analysis based on a network model of depression.

Frontiers in neuroscience January 1, 2025 Kasper Recourt, Joop Van Gerven, Nadieh Drenth et al. 1 citation

Ketamine, given intravenously at 0.5 mg/kg, rapidly reduces depression symptoms in patients with non-treatment-resistant major depressive disorder. In a randomized, double-blind, placebo-controlled crossover study with 16 patients, ketamine lowered mean MADRS scores from 21.2 before dosing to 10.3 at 24 hours, compared with placebo. Resting-state fMRI showed that ketamine altered functional connectivity only in brain circuits previously linked to depression—the corticolimbic-insular-striatal-pallidal-thalamic (CLIPST) network—at both acute (50–165 minutes) and delayed (24 hours) time points. No connectivity changes occurred outside this depression-related circuitry. The results indicate that ketamine specifically targets depression-associated neural pathways, supporting model-based analysis in future pharmaco-fMRI studies.

Comparative EEG analysis of the effects of ketamine enantiomers and metabolites in rhesus macaques.

Journal of neurophysiology April 1, 2026 Yoshihiro Iwamura, Kantaro Nishigori, Masataka Yamaguchi et al.

At a dose matching the concentration found effective for depression in humans, the anesthetic (R,S)-ketamine increased gamma power in the EEG of rhesus macaques, replicating clinical findings. The enantiomer (R)-ketamine produced a similar rise in gamma power but had weaker effects on EEG features linked to side effects. Ketamine metabolites caused only mild EEG changes, suggesting they contribute little to ketamine's EEG effects. The results indicate (R)-ketamine may have a broader therapeutic range and lower risk of adverse effects than (R,S)-ketamine.