Evidence map›Paper›PMID 36568100›Full record

ArticleFrontiers in endocrinology2022

ATP-citrate lyase inhibitor improves ectopic lipid accumulation in the kidney in a db/db mouse model.

Zishun Zhan, Aimei Li, Wei Zhang, Xueqin Wu, Jinrong He, Zhi Li, Yanchun Li, Jian Sun, Hao Zhang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. New insights into the ACLY-mediated metabolic and epigenetic interplay in macrophages.Journal of enzyme inhibition and medicinal chemistry · 2026
    Review
  3. Article
  4. Article
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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

9 authors at 3 institutions in 2 countries.

Zishun ZhanDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Aimei LiDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Wei ZhangDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xueqin WuDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jinrong HeDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhi LiDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yanchun LiDivision of Biological Sciences, Department of Medicine, University of Chicago, Chicago, Chicago, IL, United States.
Jian SunDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hao ZhangDepartment of Nephrology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Central South University · CNThird Xiangya Hospital · CNUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: We evaluated a novel treatment for obesity-related renal, an ATP-citrate lyase (ACL) inhibitor, to attenuate ectopic lipid accumulation (ELA) in the kidney and the ensuing inflammation. Materials and methods: An ACL inhibitor was administered intragastrically to 12-week-old db/db mice for 30 days. The appearance of ELA was observed by staining kidney sections with Oil Red O, and the differences in tissue lipid metabolites were assessed by mass spectrometry. The anti-obesity and renoprotection effects of ACL inhibitors were observed by histological examination and multiple biochemical assays. Results: Using the AutoDock Vina application, we determined that among the four known ACL inhibitors (SB-204990, ETC-1002, NDI-091143, and BMS-303141), BMS-303141 had the highest affinity for ACL and reduced ACL expression in the kidneys of db/db mice. We reported that BMS-303141 administration could decrease the levels of serum lipid and renal lipogenic enzymes acetyl-CoA carboxylase (ACC), fatty acid synthase (FAS), HMG-CoA reductase (HMGCR), and diminish renal ELA in db/db mice. In addition, we found that reducing ELA improved renal injuries, inflammation, and tubulointerstitial fibrosis. Conclusion: ACL inhibitor BMS-303141 protects against obesity-related renal injuries.

Indexed as

Enzyme InhibitorsKidneyAdenosine TriphosphateAnimalsInflammationMiceMultienzyme ComplexesObesityOxo-Acid-LyasesAdenosine Triphosphatecitrate (pro-3S)-lyaseEnzyme InhibitorsMultienzyme ComplexesOxo-Acid-LyasesACLATP-citrate lyaseBMS-303141ectopic lipid accumulationobesity-related nephropathyrenal inflammation

Identifiers

PMID36568100
PMCPMC9771989
OpenAlexW4311848673

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.