ArticlePsychopharmacology2026
Omega-3 fatty acids improves tamoxifen-induced sexual dysfunction in male Wistar rats by modulating NO/cGMP signaling and monoamine neurotransmitters activities.
Article in Psychopharmacology, 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.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionTamoxifen (TAM) is an off-label treatment option for men with breast cancer, infertility, and gynecomastia. Unfortunately, one of the undesirable effects of TAM is sexual dysfunction. Therefore, this study was designed to investigate the possible associated mechanisms with TAM-induced sexual dysfunction and the possible ameliorative effect of omega-3 fatty acids (O3FA). METHODOLOGY: Animals were randomly divided into control, O3FA, TAM, and TAM + O3FA. All treatment lasted for 28 days.
resultsTAM exposure impaired sperm qualities (count, motility, viability, and normal morphology) and led to a decline in serum testosterone and an increase in luteinizing hormone, follicle-stimulating hormone, prolactin, and estradiol. Furthermore, TAM led to an increase in mount, intromission, and ejaculation latencies and a decrease in their corresponding frequencies. It also led to a decrease in motivation to mate and an increase in post-ejaculatory interval. These events were associated with impaired pregnancy outcomes, hormonal imbalance, a decrease in nitric oxide/cyclic cyclic guanosine monophosphate and dopamine and an increase in acetylcholine esterase and serotonin activities. These observed TAM-induced sexual dysfunction markers were ameliorated in animals that received O3FA and TAM co-treatment.
conclusionsO3FA ameliorates TAM-induced sexual dysfunction.
Indexed as
Identifiers
40528104What 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.