Evidence map›Paper›PMID 32546086›Full record

ArticleAutophagy2021

Eicosapentaenoic acid attenuates renal lipotoxicity by restoring autophagic flux.

Takeshi Yamamoto, Yoshitsugu Takabatake, Satoshi Minami, Shinsuke Sakai, Ryuta Fujimura, Atsushi Takahashi, Tomoko Namba-Hamano, Jun Matsuda, Tomonori Kimura, Isao Matsui and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
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  4. Selective autophagy in kidney health and disease.Nature reviews. Nephrology · 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

19 authors at 5 institutions in 1 country.

Takeshi YamamotoDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Yoshitsugu TakabatakeDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0002-8912-2316
Satoshi MinamiDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Shinsuke SakaiDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Ryuta FujimuraDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Atsushi TakahashiDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Tomoko Namba-HamanoDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0002-6049-7616
Jun MatsudaDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Tomonori KimuraDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
Isao MatsuiDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0001-8378-6130
Jun-Ya KaimoriDepartment of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Osaka, Japan.
Hiroaki TakedaDivision of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Masatomo TakahashiDivision of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Yoshihiro IzumiDivision of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Takeshi BambaDivision of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Taiji MatsusakaInstitute of Medical Sciences and Department of Molecular Life Sciences, Tokai University School of Medicine, Kanagawa, Japan.
Fumio NiimuraDepartment of Pediatrics, Tokai University School of Medicine, Kanagawa, Japan.
Motoko YanagitaDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yoshitaka IsakaDepartment of Nephrology, Osaka University Graduate School of Medicine, Osaka, Japan.
The University of Osaka · JPKyushu University · JPTokai University · JPKyoto University · JPNational Institute of Biomedical Innovation, Health and Nutrition · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we identified a novel mechanism of lipotoxicity in the kidney proximal tubular cells (PTECs); lipid overload stimulates macroautophagy/autophagy for the renovation of plasma and organelle membranes to maintain the integrity of the PTECs. However, this autophagic activation places a burden on the lysosomal system, leading to a downstream suppression of autophagy, which manifests as phospholipid accumulation and inadequate acidification in lysosomes. Here, we investigated whether pharmacological correction by eicosapentaenoic acid (EPA) supplementation could restore autophagic flux and alleviate renal lipotoxicity. EPA supplementation to high-fat diet (HFD)-fed mice reduced several hallmarks of lipotoxicity in the PTECs, such as phospholipid accumulation in the lysosome, mitochondrial dysfunction, inflammation, and fibrosis. In addition to improving the metabolic syndrome, EPA alleviated renal lipotoxicity via several mechanisms. EPA supplementation to HFD-fed mice or the isolated PTECs cultured in palmitic acid (PA) restored lysosomal function with significant improvements in the autophagic flux. The PA-induced redistribution of phospholipids from cellular membranes into lysosomes and the HFD-induced accumulation of SQSTM1/p62 (sequestosome 1), an autophagy substrate, during the temporal and genetic ablation of autophagy were significantly reduced by EPA, indicating that EPA attenuated the HFD-mediated increases in autophagy demand. Moreover, a fatty acid pulse-chase assay revealed that EPA promoted lipid droplet (LD) formation and transfer from LDs to the mitochondria for beta-oxidation. Noteworthy, the efficacy of EPA on lipotoxicity is autophagy-dependent and cell-intrinsic. In conclusion, EPA counteracts lipotoxicity in the proximal tubule by alleviating autophagic numbness, making it potentially suitable as a novel treatment for obesity-related kidney diseases.

Indexed as

Acute Kidney InjuryAnimalsAutophagyDiet, High-FatEicosapentaenoic AcidKidneyKidney Tubules, ProximalLysosomesMiceMice, TransgenicPhospholipidsEicosapentaenoic AcidPhospholipidsAutophagic fluxautophagylipid dropletlysosomemitochondria

Identifiers

PMID32546086
PMCPMC8354598
OpenAlexW3035175200

What OpenQuestion holds

Textmetadata
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.