ReviewMolecular neurobiology2026
Emerging Molecular Targets and Recent Advancements for the Management of Depression.
Review in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Depression is a serious mental disorder characterized by alteration in mood, loss of interest and feeling sad, irritable, and empty. World Health Organization ranks depression as the leading cause of mental disability and is projected to become top contributor to the global disease burden by 2030. The pathogenesis of depression is very diverse, complicated, and unclear. Despite improvements in the conventional treatments, currently available options have shortfalls such as reduced efficacy, increased side effects, not suitable for prolonged usage, patient variance, resistance issues, etc. persists, which emphasize the need of exploring the emerging molecular targets. Recent research advances in neurobiology have highlighted the role of interconnected molecular targets and cellular pathways, including neural circuits, synaptic plasticity, neurotransmitter systems, and HPA axis dysregulation, in depression. These targets regulate key signaling pathways such as PI3K/Akt/mTOR, Ras-MAPK/ERK, and NF-κB, providing promising avenues for the development of novel targeted antidepressant therapies and driving a shift beyond conventional treatment strategies.This review summarizes the emerging molecular targets and recent therapeutic advancements in depression, with a prime focus on their underlying mechanisms, signaling pathways, and clinical significance. Furthermore, recent clinical successes and USFDA-approved targeted antidepressants are discussed, highlighting the growing importance of molecularly guided approaches in antidepressant drug discovery. A deeper understanding of these targets may facilitate the development of safer, more effective therapies for the management of depression in future.
Indexed as
Identifiers
42435254What Socratic holds
Registered trials
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.