Evidence mapPaperPMID 39154177Full record

ArticleLipids in health and disease2024

Pitavastatin attenuates hypercholesterolemia-induced decline in serotonin transporter availability.

Sy-Jou Chen, Rou-Ling Cho, Skye Hsin-Hsien Yeh, Min-Chien Tsai, Yi-Ping Chuang, Chih-Feng Lien, Chuang-Hsin Chiu, Yi-Wei Yeh, Chin-Sheng Lin, Kuo-Hsing Ma

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In one paragraph

Article in Lipids in health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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4 · The record

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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

10 authors.

Sy-Jou ChenDepartment of Emergency Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan. syjou.chen@gmail.com.
Rou-Ling ChoDivision of Cardiology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan.
Skye Hsin-Hsien YehSchool of Medicine, National Defense Medical Center, Taipei, Taiwan.
Min-Chien TsaiDepartment of Physiology and Biophysics, Graduate Institute of Physiology, National Defense Medical Center, Taipei, Taiwan.
Yi-Ping ChuangDepartment of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan.
Chih-Feng LienDivision of Cardiology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan.
Chuang-Hsin ChiuDepartment of Nuclear Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Yi-Wei YehDepartment of Psychiatry, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Chin-Sheng LinDivision of Cardiology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan. littlelin@gmail.com.
Kuo-Hsing MaDepartment of Biology and Anatomy, National Defense Medical Center, Taipei, 114, Taiwan. kuohsing91@yahoo.com.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHypercholesterolemia is associated with increased inflammation and impaired serotonin neurotransmission, potentially contributing to depressive symptoms. However, the role of statins, particularly pitavastatin, in modulating serotonin transporter (SERT) function within this context remains underexplored. This study aimed to investigate whether pitavastatin counteracts the neurobiological effects of hypercholesterolemia.

methodsLow-density lipoprotein receptor knockout (LDLR

resultsPitavastatin treatment in HFD-fed mice significantly reduced both total cholesterol and LDL cholesterol levels in HFD-fed mice compared to those on HFD alone. Elevated inflammatory markers such as IL-1α, MCP-1/CCL2, and TNF-α in HFD mice were notably decreased in the HFD + Pita group. PET scans showed reduced SERT availability in the brains of HFD mice; however, pitavastatin improved this in brain regions associated with mood regulation, suggesting enhanced serotonin neurotransmission. Additionally, the sucrose preference test showed a trend towards increased preference in the HFD + Pita group compared to the HFD group, indicating a potential reduction in depressive-like behavior.

conclusionOur findings demonstrate that pitavastatin not only lowers cholesterol and reduces inflammation but also enhances SERT availability, suggesting a potential role in alleviating depressive symptoms associated with hypercholesterolemia. These results highlight the multifaceted benefits of pitavastatin, extending beyond its lipid-lowering effects to potentially improving mood regulation and neurotransmitter function.

Indexed as

Diet, High-FatHypercholesterolemiaMice, Inbred C57BLQuinolinesSerotonin Plasma Membrane Transport ProteinsAnimalsBrainCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiceMice, KnockoutPositron-Emission TomographyReceptors, LDLCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorspitavastatinQuinolinesReceptors, LDLSerotonin Plasma Membrane Transport Proteins4-[18F]-ADAMDepressionHypercholesterolemiaPitavastatinPositron emission tomographySerotonin transporter (SERT)

Identifiers

PMID39154177
PMCPMC11330603

What Socratic holds

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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 Socratic graph.