Exploring the Therapeutic Potential of Ketamine and Psilocybin in Comparison to Current Treatment Regimens for Treatment-Resistant Depression, Mood Disorders, and Post-traumatic Stress Disorder in the Pediatric Population: A Narrative Review.

Exploring the Therapeutic Potential of Ketamine and Psilocybin in Comparison to Current Treatment Regimens for Treatment-Resistant Depression, Mood Disorders, and Post-traumatic Stress Disorder in the Pediatric Population: A Narrative Review.

Publication date: Aug 01, 2025

The stresses of the Coronavirus Disease of 2019 (COVID-19) pandemic highlighted the burden of psychiatric disorders within the pediatric population, revealing a pre-existing need for rapid-onset therapies that have since driven efforts to expand effective therapeutic interventions. In this narrative review, we utilized the Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) guidelines to direct our report and study selection. We explored the current-state efficacy and therapeutic potential of ketamine and psilocybin in comparison to current treatment regimens for pediatric non-psychotic disorders, including Treatment-Resistant Depression (TRD), mood disorders like anxiety and bipolar disorder, and Post-Traumatic Stress Disorder (PTSD). We chose these pediatric disorders to eliminate concerns regarding reality orientation and the use of dissociative and/or psychedelic medicines in patients who are experiencing symptoms of psychosis. Also, we briefly discuss ketamine’s more widely accepted utilization by medical providers as a pediatric anesthetic, and how this gives credence to further evaluation of ketamine’s multifaceted indications in pediatric psychiatry. Recent studies have shed light on the involvement of glutamate pathways in the pathophysiology of TRD, mood disorders, and PTSD, and both ketamine, an N-methyl-D-aspartate (NMDA) receptor antagonist, and psilocybin, a 5-hydroxytryptamine receptor 2A (5-HT2A) agonist, have emerged as promising options due to their ability to augment glutamate release. Ketamine’s use for pediatric TRD demonstrated rapid-onset relief for signs and symptoms of depression in children and adolescents, and psilocybin also decreased symptoms in patients with longstanding or refractory depression. Ketamine has been well tolerated and exhibited symptom improvements for youth with mood disorders such as anxiety and bipolar depression, while psilocybin showed promise in fostering emotional processing. In youth suffering from PTSD, ketamine-assisted psychotherapy (KAP) brought about decreases in PTSD symptom severity, though outcomes varied across populations. Psilocybin enhanced neural plasticity, allowing patients to revisit and reframe memories under therapeutic guidance, especially for those with complex or treatment-resistant PTSD. Ethical considerations are involved in the use of dissociative and hallucinogenic therapies like ketamine and psilocybin in the pediatric population, and we explore some ethical issues regarding their use. Further research exploring specific brain locations and mechanisms of action underlying glutamate modulation by ketamine and psilocybin, and the subsequent rapid-acting relief of psychiatric symptoms offered by these substances, could pave the way for innovative treatments targeting pediatric mental health disorders.

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Concepts Keywords
Coronavirus ketamine
Ht2a mood disorders
Longstanding psilocybin
Pandemic treatment-resistant depression
Psychotherapy

Semantics

Type Source Name
drug DRUGBANK Ketamine
drug DRUGBANK Psilocybine
disease MESH Depression
disease MESH Mood Disorders
disease MESH Post-traumatic Stress Disorder
pathway KEGG Coronavirus disease
disease MESH COVID-19
disease MESH psychiatric disorders
disease MESH psychotic disorders
disease MESH anxiety
disease MESH bipolar disorder
pathway REACTOME Release
disease MESH refractory depression
disease IDO symptom
pathway REACTOME Reproduction
drug DRUGBANK Methionine
drug DRUGBANK gamma-Aminobutyric acid
disease MESH abnormalities
disease MESH emergence agitation
drug DRUGBANK Dimethyltryptamine
drug DRUGBANK Alkaline Phosphatase
drug DRUGBANK Serotonin
pathway REACTOME Serotonin receptors
disease IDO protein
drug DRUGBANK Isoxaflutole
drug DRUGBANK Propofol
drug DRUGBANK Sevoflurane
disease MESH postoperative complications
disease MESH respiratory depression
disease IDO country
disease MESH Contraindications
disease MESH tachycardia
disease MESH laryngospasm
drug DRUGBANK Oxygen
drug DRUGBANK Midazolam
drug DRUGBANK Esketamine
drug DRUGBANK Fenamole
disease IDO blood
disease IDO replication
disease MESH hypotension
disease MESH hallucinations
disease IDO history
disease MESH mania
disease MESH suicidal ideations
disease MESH dissociation
disease MESH substance abuse
disease MESH neurological disorder
disease MESH Major Depressive Disorder
disease MESH Autism Spectrum Disorder
disease MESH Suicide
disease MESH Intellectual disability
disease MESH unipolar depression
disease MESH autism
disease MESH Schizophrenia
disease IDO intervention
disease MESH anxiety disorders
disease MESH personality disorders
disease MESH syndrome
drug DRUGBANK Indoleacetic acid
disease MESH delusions
disease MESH bulimia
disease MESH anorexia nervosa
disease MESH alcohol abuse
disease MESH hypertension
disease MESH panic
disease MESH emergency
drug DRUGBANK Coenzyme M
drug DRUGBANK Factor IX Complex (Human)
drug DRUGBANK Nandrolone phenpropionate
disease MESH social anxiety disorders
disease MESH Acute Stress Disorder
drug DRUGBANK Trestolone
disease MESH psychological distress

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