Evidence map›Paper›PMID 26262615›Full record

ReviewInternational journal of molecular sciences2015

Functional Selectivity and Antidepressant Activity of Serotonin 1A Receptor Ligands.

Zdzisław Chilmonczyk, Andrzej Jacek Bojarski, Andrzej Pilc, Ingebrigt Sylte

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

22 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
  2. Pharmaco-Multiomics: A New Frontier in Precision Psychiatry.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Association ofNeuropsychiatric disease and treatment · 2024
    Article
  5. Article
  6. Article
  7. The selective 5-HTPsychopharmacology · 2021
    Article
  8. Article
  9. Review
  10. The functional cooperation of 5-HTPharmacological reports : PR · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Serotonin Transporter (Frontiers in genetics · 2019
    Article
  16. Oncotoxic Properties of Serotonin Transporter Inhibitors and 5-HTInternational journal of molecular sciences · 2018
    Article
  17. Article
  18. HBK-17, a 5-HTFrontiers in pharmacology · 2018
    Article
  19. Serotonin and brain function: a tale of two receptors.Journal of psychopharmacology (Oxford, England) · 2017
    Review
  20. Review
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

4 authors at 4 institutions in 2 countries.

Zdzisław ChilmonczykNational Medicines Institute, Chełmska 30/34, 00-725 Warszawa, Poland. z.chilmonczyk@nil.gov.pl.
Andrzej Jacek BojarskiInstitute of Pharmacology, Polish Academy of Sciences, Smetna 12, 31-343 Kraków, Poland. bojarski@if-pan.krakow.pl.
Andrzej PilcInstitute of Pharmacology, Polish Academy of Sciences, Smetna 12, 31-343 Kraków, Poland. nfpilc@cyf-kr.edu.pl.
Ingebrigt SylteFaculty of Health Sciences, University of Tromsø-The Arctic University of Norway, No-9037 Tromsø, Norway. ingebrigt.sylte@uit.no.
Maj Institute of Pharmacology · PLPolish Academy of Sciences · PLRzeszów University · PLUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serotonin (5-HT) is a monoamine neurotransmitter that plays an important role in physiological functions. 5-HT has been implicated in sleep, feeding, sexual behavior, temperature regulation, pain, and cognition as well as in pathological states including disorders connected to mood, anxiety, psychosis and pain. 5-HT1A receptors have for a long time been considered as an interesting target for the action of antidepressant drugs. It was postulated that postsynaptic 5-HT1A agonists could form a new class of antidepressant drugs, and mixed 5-HT1A receptor ligands/serotonin transporter (SERT) inhibitors seem to possess an interesting pharmacological profile. It should, however, be noted that 5-HT1A receptors can activate several different biochemical pathways and signal through both G protein-dependent and G protein-independent pathways. The variables that affect the multiplicity of 5-HT1A receptor signaling pathways would thus result from the summation of effects specific to the host cell milieu. Moreover, receptor trafficking appears different at pre- and postsynaptic sites. It should also be noted that the 5-HT1A receptor cooperates with other signal transduction systems (like the 5-HT1B or 5-HT2A/2B/2C receptors, the GABAergic and the glutaminergic systems), which also contribute to its antidepressant and/or anxiolytic activity. Thus identifying brain specific molecular targets for 5-HT1A receptor ligands may result in a better targeting, raising a hope for more effective medicines for various pathologies.

Indexed as

AnimalsAntidepressive AgentsDepressionDepressive DisorderHumansLigandsMAP Kinase Signaling SystemMolecular Targeted TherapyPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, Serotonin, 5-HT1ASerotoninSerotonin 5-HT1 Receptor AgonistsSignal TransductionAntidepressive AgentsLigandsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, Serotonin, 5-HT1ASerotoninSerotonin 5-HT1 Receptor Agonistsantidepressant activityreceptor traffickingserotonin 1A receptors

Identifiers

PMID26262615
PMCPMC4581256
OpenAlexW1920429098

What OpenQuestion 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 OpenQuestion graph.