ReviewPharmacological reports : PR2026
Sigma receptor ligands in selected affective disorders, psychoses, and addictions - a narrative review.
Review in Pharmacological reports : PR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sigma receptors (SRs), comprising the sigma 1 (S1R) and sigma 2 (S2R) subtypes, represent a distinct class of intracellular proteins that differ fundamentally from classical neurotransmitter receptors. S1Rs act as ligand-operated molecular chaperones primarily localized at mitochondria-associated membranes (MAM) of the endoplasmic reticulum (ER), whereas S2Rs, identified as transmembrane protein 97 (TMEM97), function as modulators of cellular homeostasis. Both subtypes are densely expressed in brain regions critical for emotional and cognitive processing, including the prefrontal cortex (PFC), hippocampus (HIP), amygdala (AMG), and basal ganglia. SRs play a pivotal role in regulating neuronal excitability, synaptic plasticity, and ER stress responses, thereby influencing oxidative stress, synaptogenesis, and neuronal survival. Moreover, their interactions with endogenous neurosteroids and the immune-endocrine system highlight their involvement in complex neuropsychiatric pathophysiology. Consequently, SRs are increasingly recognized as promising targets for pharmacological intervention. Preclinical evidence indicates that S1R agonists exert antidepressant, anxiolytic, and pro-cognitive effects, whereas S1R antagonism or genetic deletion induces behavioural phenotypes relevant to depression and schizophrenia. S2R modulation, in turn, influences psychostimulant sensitivity and emotional regulation, although its underlying mechanisms remain less well defined. Notably, the clinical efficacy of several widely used antidepressants (e.g., fluvoxamine) and antipsychotics have been increasingly attributed to their significant affinity for SRs, suggesting that SR engagement may contribute to their therapeutic profiles. This narrative review synthesizes core molecular and neurophysiological findings and critically evaluates the potential of SR-targeting compounds as next-generation pharmacological strategies for treatment-resistant depression, psychotic disorders, and addiction. Given the continuous emergence of new research, this work provides an updated overview of the current state of knowledge for both researchers and clinicians.
Indexed as
Identifiers
41945312What OpenQuestion 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 OpenQuestion graph.