Evidence map›Paper›PMID 27618957›Full record

ArticleScientific reports2016

Chronic Moderate Alcohol Intakes Accelerate SR-B1 Mediated Reverse Cholesterol Transport.

Menghua Li, Yan Diao, Ying Liu, Hui Huang, Yanze Li, Peizhu Tan, Huan Liang, Qi He, Junhui Nie, Xingli Dong and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  7. Antihypercholesterolemic and antiatherosclerotic potencies ofJournal of advanced pharmaceutical technology & research
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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

13 authors at 4 institutions in 1 country.

Menghua LiDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Yan DiaoDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Ying LiuDepartment of Gastroenterology, Heilongjiang Province Hospital, Harbin, China.
Hui HuangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Yanze LiDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Peizhu TanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Huan LiangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Qi HeDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Junhui NieDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Xingli DongDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Yang WangDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Lingyun ZhouDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Xu GaoDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, China.
Harbin Medical University · CNHeilongjiang Provincial Hospital · CNState Intellectual Property Office · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol is essential for all animal life. However, a high level of cholesterol in the body is strongly associated with the progression of various severe diseases. In our study, the potential involvement of alcohol in the regulation of high density lipoprotein (HDL) receptor scavenger receptor class B and type I (SR-B1)-mediated reverse cholesterol transport was investigated. We separated male C57BL/6 mice into four diets: control, alcohol, Control + HC and alcohol + HC. The SR-B1 level and 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate- high- density lipoprotein (DiI-HDL) uptake were also measured in AML12 cells and HL7702 cells treated with alcohol. The control + HC diet led to increased hepatic triglyceride and cholesterol levels while alcohol + HC led no significant change. Compared with that of the control group, the SR-B1 mRNA level was elevated by 27.1% (P < 0.05), 123.8% (P < 0.001) and 343.6% (P < 0.001) in the alcohol, control + HC and alcohol + HC groups, respectively. In AML12 and HL7702 cells, SR-B1 level and DiI-HDL uptake were repressed by SR-B1 siRNA or GW9662. However, these effects were reversed through alcohol treatment. These data suggest that a moderate amount of alcohol plays a novel role in reverse cholesterol transport, mainly mediated by PPARγ and SR-B1.

Indexed as

Alcohol DrinkingAnimalsBiological Transport, ActiveCell LineCholesterolLipoproteins, HDLLiverMicePPAR gammaRNA, MessengerScavenger Receptors, Class BTriglyceridesCholesterolLipoproteins, HDLPPAR gammaRNA, MessengerScarb1 protein, mouseScavenger Receptors, Class BTriglycerides

Identifiers

PMID27618957
PMCPMC5020497
OpenAlexW2519226788

What OpenQuestion holds

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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.