Evidence map›Paper›PMID 41516220›Full record

ReviewInternational journal of molecular sciences2025

Molecular Mechanisms of Emerging Antidepressant Strategies: From Ketamine to Neuromodulation.

Mateusz Kowalczyk, David Aebisher, Jakub Szpara, Sara Czech, Dorota Bartusik-Aebisher, Gabriela Henrykowska

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mateusz KowalczykMediPsyche Medical Center, J. Kolinskiego 27, 91-849 Lodz, Poland.
David AebisherDepartment of Photomedicine and Physical Chemistry, Collegium Medicum, Faculty of Medicine, Rzeszów University, 35-310 Rzeszów, Poland.ORCID 0000-0002-2661-6570
Jakub SzparaEnglish Division Science Club, Collegium Medicum, Faculty of Medicine, Rzeszów University, 35-310 Rzeszów, Poland.
Sara CzechEnglish Division Science Club, Collegium Medicum, Faculty of Medicine, Rzeszów University, 35-310 Rzeszów, Poland.
Dorota Bartusik-AebisherDepartment of Biochemistry and General Chemistry, Collegium Medicum, Faculty of Medicine, Rzeszów University, 35-310 Rzeszów, Poland.ORCID 0000-0002-5557-5464
Gabriela HenrykowskaDepartment of Epidemiology and Public Health, Faculty of Medicine, Medical University of Lodz, T. Kosciuszki 4, 90-419 Lodz, Poland.ORCID 0000-0002-9277-0875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is a common, debilitating, and potentially life-threatening mental disorder affecting individuals across all age groups and populations. It represents one of the major challenges of contemporary medicine. It is estimated that more than 300 million people worldwide are affected, and patients with major depressive disorder (MDD) exhibit a significantly increased risk of suicide, underscoring the urgent need for effective and long-lasting therapeutic strategies. Growing evidence indicates that the pathophysiology of depression involves a complex interplay of genetic vulnerability, chronic stress, dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis, neuroinflammation, oxidative stress, mitochondrial dysfunction, and impaired synaptic plasticity, collectively contributing to symptom heterogeneity and treatment resistance. In this review, we synthesize data derived from PubMed, Google Scholar, and ClinicalTrials.gov databases concerning pharmacological and non-pharmacological treatment strategies, with particular emphasis on their cellular and molecular mechanisms of action. We present currently used classes of antidepressant drugs, including selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), and monoamine oxidase inhibitors (MAOIs), discussing their limitations in the context of contemporary pathophysiological models of depression. We then focus on emerging therapies targeting the glutamatergic, GABAergic, and dopaminergic systems, including ketamine, esketamine, (R)-ketamine, the dextromethorphan-bupropion combination (DMX-BUP), neurosteroids (zuranolone, brexanolone), as well as selective serotonin receptor modulators (gepirone ER) and dopaminergic modulators (cariprazine). The review is complemented by a discussion of non-pharmacological neuromodulatory approaches, such as transcranial magnetic stimulation (TMS), transcranial direct current stimulation (tDCS), and photobiomodulation. Rather than providing another summary of clinical response indicators, this article integrates the molecular underpinnings of novel antidepressant agents and neuromodulation techniques with current concepts of depression pathophysiology, highlighting their relevance for the development of precise, mechanistically targeted, and multimodal treatment strategies.

Indexed as

Antidepressive AgentsKetamineMajor Depressive DisorderNeurotransmitter AgentsAnimalsHumansAntidepressive AgentsKetamineNeurotransmitter Agentsdepressiondepressive disordermolecular mechanismsneuromodulationnovel antidepressant drugs

Identifiers

PMID41516220
PMCPMC12785913

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.