Evidence map›Paper›PMID 25733327›Full record

ArticleAtherosclerosis2015

Inhibition of soluble epoxide hydrolase in mice promotes reverse cholesterol transport and regression of atherosclerosis.

Li Shen, Hongchun Peng, Ran Peng, Qingsong Fan, Shuiping Zhao, Danyan Xu, Christophe Morisseau, Nipavan Chiamvimonvat, Bruce D Hammock

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

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  18. CYP450-derived oxylipins mediate inflammatory resolution.Proceedings of the National Academy of Sciences of the United States of America · 2016
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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.

Li ShenDepartment of Cardiology, Internal Medicine, Xiangya Second Hospital, Central South University, Changsha, 410011, PR China.
Hongchun PengDepartment of Orthopaedics and Emergency, Changsha Central Hospital, Changsha, 410011, PR China.
Ran PengDepartment of Cardiology, Internal Medicine, Xiangya Second Hospital, Central South University, Changsha, 410011, PR China.
Qingsong FanDepartment of Pathology, Xiangya Second Hospital, Central South University, Changsha, Hunan Province, 410001, PR China.
Shuiping ZhaoDepartment of Cardiology, Internal Medicine, Xiangya Second Hospital, Central South University, Changsha, 410011, PR China.
Danyan XuDepartment of Cardiology, Internal Medicine, Xiangya Second Hospital, Central South University, Changsha, 410011, PR China. Electronic address: xudanyan02@sina.com.
Christophe MorisseauDepartment of Entomology and Comprehensive Cancer Center, University of California, Davis, CA, 95616, USA.
Nipavan ChiamvimonvatDivision of Cardiovascular Medicine, Department of Internal Medicine, University of California, Davis, CA, 95616, USA.
Bruce D HammockDepartment of Entomology and Comprehensive Cancer Center, University of California, Davis, CA, 95616, USA.
Central South University · CNUniversity of California, Davis · USChangsha Central Hospital · CN

Funding

Functional Interactions of Cardiac Ion ChannelsR01HL085844 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN · 2007 to 2025
$7.3M
Translational Study of Cardiac DysfunctionR01HL085727 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN, SIRISH, PADMINI · 2008 to 2022
$5.7M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR01ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1985 to 2018
$4.0M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR37ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1998 to 2007
$3.0M
Decoding the enigma of cardiac amplificationR01HL137228 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHIAMVIMONVAT, NIPAVAN · 2017 to 2020
$2.2M
Regulation of ion channels in the heartI01BX000576 · VA · VA NORTHERN CALIFORNIA HEALTH CARE SYS · PI CHIAMVIMONVAT, NIPAVAN · 2009 to 2019
–
BLRD VA I01 BX000576CSRD VA I01 CX001490NHLBI NIH HHS R01 HL085727NHLBI NIH HHS R01 HL085844NHLBI NIH HHS R01 HL137228NIEHS NIH HHS ES02710NIEHS NIH HHS R01 ES002710NIEHS NIH HHS R37 ES002710
6 · The paper itself

Abstract

Adipose tissue is the body largest free cholesterol reservoir and abundantly expresses ATP binding cassette transporter A1 (ABCA1), which maintains plasma high-density lipoprotein (HDL) levels. HDLs have a protective role in atherosclerosis by mediating reverse cholesterol transport (RCT). Soluble epoxide hydrolase (sEH) is a cytosolic enzyme whose inhibition has various beneficial effects on cardiovascular disease. The sEH is highly expressed in adipocytes, and it converts epoxyeicosatrienoic acids (EETs) into less bioactive dihydroxyeicosatrienoic acids. We previously showed that increasing EETs levels with a sEH inhibitor (sEHI) (t-AUCB) resulted in elevated ABCA1 expression and promoted ABCA1-mediated cholesterol efflux from 3T3-L1 adipocytes. The present study investigates the impacts of t-AUCB in mice deficient for the low density lipoprotein (LDL) receptor (Ldlr(-/-) mice) with established atherosclerotic plaques. The sEH inhibitor delivered in vivo for 4 weeks decreased the activity of sEH in adipose tissue, enhanced ABCA1 expression and cholesterol efflux from adipose depots, and consequently increased HDL levels. Furthermore, t-AUCB enhanced RCT to the plasma, liver, bile and feces. It also showed the reduction of plasma LDL-C levels. Consistently, t-AUCB-treated mice showed reductions in the size of atherosclerotic plaques. These studies establish that raising adipose ABCA1 expression, cholesterol efflux, and plasma HDL levels with t-AUCB treatment promotes RCT, decreasing LDL-C and atherosclerosis regression, suggesting that sEH inhibition may be a promising strategy to treat atherosclerotic vascular disease.

Indexed as

Adipose TissueAnimalsAortic DiseasesAtherosclerosisATP Binding Cassette Transporter 1BenzoatesBiomarkersCholesterolCholesterol, HDLCholesterol, LDLDisease Models, AnimalDose-Response Relationship, DrugEnzyme InhibitorsEpoxide HydrolasesMaleMice, Inbred C57BL4-(4-(3-adamantan-1-ylureido)cyclohexyloxy)benzoic acidAbca1 protein, mouseATP Binding Cassette Transporter 1BenzoatesBiomarkersCholesterolCholesterol, HDLCholesterol, LDLEnzyme InhibitorsEphx2 protein, mouseEpoxide HydrolasesReceptors, LDLUreaATP binding cassette transporter A1Epoxyeicosatrienoic acidsHigh density lipoproteinReverse cholesterol transportSoluble epoxide hydrolase

Identifiers

PMID25733327
PMCPMC4527317
OpenAlexW2029862970

What OpenQuestion holds

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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.