Evidence map›Paper›PMID 39338367›Full record

ReviewPharmaceuticals (Basel, Switzerland)2024

Association of the Serotonin and Kynurenine Pathways as Possible Therapeutic Targets to Modulate Pain in Patients with Fibromyalgia.

Alfonso Alfaro-Rodríguez, Samuel Reyes-Long, Ernesto Roldan-Valadez, Maykel González-Torres, Herlinda Bonilla-Jaime, Cindy Bandala, Alberto Avila-Luna, Antonio Bueno-Nava, Elizabeth Cabrera-Ruiz, Pedro Sanchez-Aparicio and 3 more

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–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

17 citing papers in PubMed.

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  4. Sublingual Cyclobenzaprine: First Approval.Clinical drug investigation · 2026
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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

13 authors.

Alfonso Alfaro-RodríguezDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0000-0002-4599-1253
Samuel Reyes-LongDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0000-0002-8916-0814
Ernesto Roldan-ValadezDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0000-0002-7116-5289
Maykel González-TorresConahcyt & Biotechnology Laboratory, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 03940, Mexico.ORCID 0000-0003-3899-4410
Herlinda Bonilla-JaimeDepartment of Reproductive Biology, Universidad Autónoma Metropolitana Iztapalapa, Mexico City 09340, Mexico.
Cindy BandalaEscuela Superior de Medicina, Instituto Politécnico Nacional, Mexico City 11340, Mexico.
Alberto Avila-LunaDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.
Antonio Bueno-NavaDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0000-0003-0291-4554
Elizabeth Cabrera-RuizDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0009-0008-9638-3638
Pedro Sanchez-AparicioPharmacology Department, Facultad de Medicina Veterinaria, Universidad Autónoma del Estado de México, Toluca 50090, Mexico.
Angélica González MacielLaboratory of Cell and Tissue Morphology, Instituto Nacional de Pediatría, Mexico City 04530, Mexico.ORCID 0000-0003-1909-9146
Ana Lilia Dotor-LlerenaDivision of Clinic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.
José Luis Cortes-AltamiranoDivision of Basic Neurosciences, Instituto Nacional de Rehabilitación, "Luis Guillermo Ibarra Ibarra", Mexico City 14389, Mexico.ORCID 0000-0002-9410-8535

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibromyalgia (FM) is a disorder characterized by widespread chronic pain, significant depression, and various neural abnormalities. Recent research suggests a reciprocal exacerbation mechanism between chronic pain and depression. In patients with FM, dysregulation of tryptophan (Trp) metabolism has been identified. Trp, an essential amino acid, serves as a precursor to serotonin (5-HT), a neuromodulator that influences mood, appetite, sleep, and pain perception through the receptors 5-HT1, 5-HT2, and 5-HT3. Additionally, Trp is involved in the kynurenine pathway, a critical route in the immune response, inflammation, and production of neuroactive substances and nicotinamide adenine dinucleotide (NAD+). The activation of this pathway by pro-inflammatory cytokines, such as tumor necrosis factor α (TNF-α) and interferon gamma (IFN-γ), leads to the production of kynurenic acid (KYNA), which has neuroprotective properties, and quinolinic acid (QA), which is neurotoxic. These findings underscore the crucial balance between Trp metabolism, 5-HT, and kynurenine, where an imbalance can contribute to the dual burden of pain and depression in patients with FM. This review proposes a novel therapeutic approach for FM pain management, focusing on inhibiting QA synthesis while co-administering selective serotonin reuptake inhibitors to potentially increase KYNA levels, thus dampening pain perception and improving patient outcomes.

Indexed as

5-HT1A5-HT25-HT35-HTTkynurenine acidquinolinic acidtryptophan

Identifiers

PMID39338367
PMCPMC11434812

What OpenQuestion holds

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Registered trials

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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.