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Elisabetta C. del Re

2 papers in the library · 111 citations · publishing 2020-2024

Papers

Real-time fMRI neurofeedback reduces auditory hallucinations and modulates resting state connectivity of involved brain regions: Part 2: Default mode network -preliminary evidence

Psychiatry Research January 14, 2020 Clemens C C Bauer, Kana Okano, Satrajit Ghosh et al. 87 citations

Auditory hallucinations in schizophrenia are linked to overactivity and hyperconnectivity in the default mode network and reduced anticorrelation with the central executive network. Patients were trained with real-time fMRI neurofeedback and meditation strategies to modulate these networks. The intervention reduced default mode network hyperconnectivity and increased anticorrelation between the default mode and central executive networks. Changes in individual default mode network connectivity correlated with reductions in auditory hallucination frequency and severity. This provides the first empirical evidence that meditation-enhanced neurofeedback can directly alter resting state network activity and reduce auditory hallucinations.

Effective action of silymarin against ketamine-induced schizophrenia in male mice: Insight into the biochemical and molecular mechanisms of action.

Journal of Psychiatric Research November 1, 2024 Benneth Ben-Azu, Aliance R Fokoua, Olajide S Annafi et al. 24 citations

Silymarin, a polyphenolic flavonoid with neuroprotective functions, prevented and reversed schizophrenia-like behaviors in mice given ketamine, an NMDA antagonist that induces neurochemical dysregulation, neuroimmune stress, and oxidative stress. In a preventive-reversal model, silymarin (50 and 100 mg/kg) reduced ketamine-induced increases in dopamine, serotonin, acetylcholinesterase, malondialdehyde, and nitrite in the striatum, prefrontal cortex, and hippocampus. It improved hyperlocomotion, stereotypy, memory, and social impairments without causing catalepsy. Silymarin also lowered inflammatory markers (myeloperoxidase, tumor-necrosis factor-α, interleukin-6) and normalized decreased brain-derived neurotrophic factor, glutathione, catalase, and superoxide-dismutase levels. The antipsychotic effect may involve normalization of neurochemical and neurotrophic changes.