Evidence map›Paper›PMID 25251395›Full record

ArticlePloS one2014

Oral supplementation with non-absorbable antibiotics or curcumin attenuates western diet-induced atherosclerosis and glucose intolerance in LDLR-/- mice--role of intestinal permeability and macrophage activation.

Siddhartha S Ghosh, Jinghua Bie, Jing Wang, Shobha Ghosh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 5 pooled it
4.6field-weighted citation impact, top 6% 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

93 citing papers in PubMed, 5 syntheses or guidelines pooled it, 157 citations in OpenAlex.

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33 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Siddhartha S GhoshDepartment of Internal Medicine, Virginia Commonwealth University Medical Center, Richmond, Virginia, United States of America.
Jinghua BieDepartment of Internal Medicine, Virginia Commonwealth University Medical Center, Richmond, Virginia, United States of America.
Jing WangDepartment of Internal Medicine, Virginia Commonwealth University Medical Center, Richmond, Virginia, United States of America.
Shobha GhoshDepartment of Internal Medicine, Virginia Commonwealth University Medical Center, Richmond, Virginia, United States of America.
Virginia Commonwealth University Medical Center · US

Funding

Cholesterol Ester Hydrolysis and Cholesterol EffluxR01HL069946 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GHOSH, SHOBHA · 2003 to 2012
$3.1M
Hepatic Cholesteryl Ester Metabolism and Cholesterol EliminationR01HL097346 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GHOSH, SHOBHA · 2010 to 2013
$1.5M
NHLBI NIH HHS HL069946NHLBI NIH HHS HL097346NHLBI NIH HHS R01 HL069946NHLBI NIH HHS R01 HL097346
6 · The paper itself

Abstract

Association between circulating lipopolysaccharide (LPS) and metabolic diseases (such as Type 2 Diabetes and atherosclerosis) has shifted the focus from Western diet-induced changes in gut microbiota per se to release of gut bacteria-derived products into circulation as the possible mechanism for the chronic inflammatory state underlying the development of these diseases. Under physiological conditions, an intact intestinal barrier prevents this release of LPS underscoring the importance of examining and modulating the direct effects of Western diet on intestinal barrier function. In the present study we evaluated two strategies, namely selective gut decontamination and supplementation with oral curcumin, to modulate Western-diet (WD) induced changes in intestinal barrier function and subsequent development of glucose intolerance and atherosclerosis. LDLR-/- mice were fed WD for 16 weeks and either received non-absorbable antibiotics (Neomycin and polymyxin) in drinking water for selective gut decontamination or gavaged daily with curcumin. WD significantly increased intestinal permeability as assessed by in vivo translocation of FITC-dextran and plasma LPS levels. Selective gut decontamination and supplementation with curcumin significantly attenuated the WD-induced increase in plasma LPS levels (3.32 vs 1.90 or 1.51 EU/ml, respectively) and improved intestinal barrier function at multiple levels (restoring intestinal alkaline phosphatase activity and expression of tight junction proteins, ZO-1 and Claudin-1). Consequently, both these interventions significantly reduced WD-induced glucose intolerance and atherosclerosis in LDLR-/- mice. Activation of macrophages by low levels of LPS (50 ng/ml) and its exacerbation by fatty acids is likely the mechanism by which release of trace amounts of LPS into circulation due to disruption of intestinal barrier function induces the development of these diseases. These studies not only establish the important role of intestinal barrier function, but also identify oral supplementation with curcumin as a potential therapeutic strategy to improve intestinal barrier function and prevent the development of metabolic diseases.

Indexed as

Macrophage ActivationAdministration, OralAnimalsAnti-Bacterial AgentsAtherosclerosisCurcuminDiet, WesternIntestinal MucosaLipopolysaccharidesMiceMice, KnockoutNF-kappa BReceptors, LDLAnti-Bacterial AgentsCurcuminLipopolysaccharidesNF-kappa BReceptors, LDL

Identifiers

PMID25251395
PMCPMC4177397
OpenAlexW2033820020

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 OpenQuestion graph.