Evidence map›Paper›PMID 25060692›Full record

ArticleMetabolism: clinical and experimental2014

Shifts in dietary carbohydrate-lipid exposure regulate expression of the non-alcoholic fatty liver disease-associated gene PNPLA3/adiponutrin in mouse liver and HepG2 human liver cells.

Lei Hao, Kyoko Ito, Kuan-Hsun Huang, Sudathip Sae-tan, Joshua D Lambert, A Catharine Ross

Open access · greenAbstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  13. Insights into the Role of PPARβ/δ in NAFLD.International journal of molecular sciences · 2018
    Review
  14. Non-alcoholic fatty liver disease phosphoproteomics: A functional piece of the precision puzzle.Hepatology research : the official journal of the Japan Society of Hepatology · 2017
    Article
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  17. Review
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

6 authors at 1 institution in 1 country.

Lei HaoDepartment of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802 USA.
Kyoko ItoDepartment of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802 USA.
Kuan-Hsun HuangDepartment of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802 USA.
Sudathip Sae-tanDepartment of Food Science, The Pennsylvania State University, University Park, PA 16802 USA.
Joshua D LambertDepartment of Food Science, The Pennsylvania State University, University Park, PA 16802 USA.
A Catharine RossDepartment of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802 USA; Center for Immunology and Infectious Disease, The Pennsylvania State University, University Park, PA 16802 USA. Electronic address: acr6@psu.edu.
Pennsylvania State University · US

Funding

Molecular Regulation of LRAT and CYP26 in Lung and LiverR01CA090214 · NCI · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI ROSS, A. CATHARINE · 2001 to 2012
$2.6M
Fatty Liver Preventive Effects and High Dose Hepatotoxicity of Tea PolyphenolsR01AT004678 · NCCIH · PENNSYLVANIA STATE UNIVERSITY, THE · PI LAMBERT, JOSHUA D · 2009 to 2013
$1.7M
NCCIH NIH HHS NIH AT004678NCCIH NIH HHS R01 AT004678NCI NIH HHS R01 CA090214PHS HHS NIHCA90214
6 · The paper itself

Abstract

objectivePatatin-like phospholipase domain containing 3 (PNPLA3, adiponutrin) has been identified as a modifier of lipid metabolism. To better understand the physiological role of PNPLA3/adiponutrin, we have investigated its regulation in intact mice and human hepatocytes under various nutritional/metabolic conditions. MATERIAL/

methodsPNPLA3 gene expression was determined by real-time PCR in liver of C57BL/6 mice after dietary treatments and in HepG2 cells exposed to various nutritional/metabolic stimuli. Intracellular lipid content was determined in HepG2 cells after siRNA-mediated knockdown of PNPLA3.

resultsIn vivo, mice fed a high-carbohydrate (HC) liquid diet had elevated hepatic lipid content, and PNPLA3 mRNA and protein expression, compared to chow-fed mice. Elevated expression was completely abrogated by addition of unsaturated lipid emulsion to the HC diet. By contrast, in mice with high-fat diet-induced steatosis, Pnpla3 expression did not differ compared to low-fat fed mice. In HepG2 cells, Pnpla3 expression was reversibly suppressed by glucose depletion and increased by glucose refeeding, but unchanged by addition of insulin and glucagon. Several unsaturated fatty acids each significantly decreased Pnpla3 mRNA, similar to lipid emulsion in vivo. However, Pnpla3 knockdown in HepG2 cells did not alter total lipid content in high glucose- or oleic acid-treated cells.

conclusionsOur results provide evidence that PNPLA3 expression is an early signal/signature of carbohydrate-induced lipogenesis, but its expression is not associated with steatosis per se. Under lipogenic conditions due to high-carbohydrate feeding, certain unsaturated fatty acids can effectively suppress both lipogenesis and PNPLA3 expression, both in vivo and in a hepatocyte cell line.

Indexed as

AnimalsCell Line, TumorDietary CarbohydratesDiet, High-FatFatty LiverGene ExpressionGlucagonGlucoseHepatocytesHep G2 CellsHumansInsulinLipid MetabolismLipidsLipogenesisLiveradiponutrinDietary CarbohydratesGlucagonGlucoseInsulinLipidsMembrane ProteinsGlucoseLipid emulsionNonalcoholic fatty liver diseasePatatin-like phospholipase domain containing 3

Identifiers

PMID25060692
PMCPMC4175036
OpenAlexW2091760532

What OpenQuestion holds

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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.