Evidence map›Paper›PMID 30585252›Full record

ArticleInternational journal of molecular sciences2018

R-Fluoxetine Increases Melanin Synthesis Through a 5-HT1A/2A Receptor and p38 MAPK Signaling Pathways.

Li Liu, Mengsi Fu, Siran Pei, Liangliang Zhou, Jing Shang

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06138509 (Role of Peripheral Serotonin in Oculocutaneous Albinism), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 25% 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.

NCT06138509 recruitingnot on this mapstarted 2024, after this paper: background citation

Role of Peripheral Serotonin in Oculocutaneous Albinism

TypeobservationalSponsorAssistance Publique - Hôpitaux de ParisRan2024 to 2026Enrolled160ConditionsOculocutaneous AlbinismArmsDosage of serotonin and metabolites, Blood parameters
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  9. Chronic salmon calcitonin exerts an antidepressant effectFrontiers in molecular neuroscience · 2023
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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

5 authors at 1 institution in 1 country.

Li LiuState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. lilcpu@hotmail.com.
Mengsi FuState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. 15151826073@163.com.
Siran PeiState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. peisiran@hotmail.com.
Liangliang ZhouState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. zhoulliang@163.com.
Jing ShangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China. shangjing21cn@163.com.
China Pharmaceutical University · CN

Funding

Applied Basic Research Programs of Qinghai Province 2015-ZJ-733National Natural Science Foundation of China 81303185
6 · The paper itself

Abstract

Fluoxetine, a member of the class of selective serotonin reuptake inhibitors, is a racemic mixture and has an anxiolytic effect in rodents. Previously, we have shown that fluoxetine can up-regulate melanin synthesis in B16F10 melanoma cells and normal human melanocytes (NMHM). However, the role of r-fluoxetine and s-fluoxetine, in the regulation of melanin synthesis, is still unknown. Here, we show how r-fluoxetine plays a critical role in fluoxetine enhancing melanogenesis, both in vivo and vitro, by up-regulating tyrosinase (TYR) and the microphthalmia-associated transcription factor (MITF) expression, whereas, s-fluoxetine does not show any effect in the vivo and vitro systems. In addition, we found that r-fluoxetine induced melanin synthesis through the serotonin1A receptor (5-HT1A) and serotonin 2A receptor (5-HT2A). Furthermore, r-fluoxetine increased the phosphorylation of p38 mitogen-activated protein kinase (p38 MAPK), without affecting the phosphorylation of extracellularly responsive kinase (ERK1/2) and c-Jun N-terminal kinase (JNK). These data suggest that r-fluoxetine may be used as a drug for skin hypopigmentation disorders.

Indexed as

AnimalsCell Line, TumorEmbryo, NonmammalianFluoxetineMelaninsMelanocytesMiceMicrophthalmia-Associated Transcription FactorMonophenol Monooxygenasep38 Mitogen-Activated Protein KinasesPhosphorylationPromoter Regions, GeneticReceptor, Serotonin, 5-HT1AReceptor, Serotonin, 5-HT2ASelective Serotonin Reuptake InhibitorsSignal TransductionFluoxetineMelaninsMicrophthalmia-Associated Transcription FactorMonophenol Monooxygenasep38 Mitogen-Activated Protein KinasesReceptor, Serotonin, 5-HT1AReceptor, Serotonin, 5-HT2ASelective Serotonin Reuptake InhibitorsZebrafish Proteinsmelaninr-fluoxetinezebrafish

Identifiers

PMID30585252
PMCPMC6337216
OpenAlexW2906300393

What OpenQuestion holds

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LicenceCC BY
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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.