Evidence map›Paper›PMID 26881897›Full record

ArticleMetabolic syndrome and related disorders2016

Effects of Nonpurified and Choline Supplemented or Nonsupplemented Purified Diets on Hepatic Steatosis and Methionine Metabolism in C3H Mice.

Raisa Syed, Noreene M Shibata, Kusum K Kharbanda, Ruijun J Su, Kristin Olson, Amy Yokoyama, John C Rutledge, Kenneth J Chmiel, Kyoungmi Kim, Charles H Halsted and 1 more

Open access · greenAbstract read
In one paragraph

Article in Metabolic syndrome and related disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Hepatic oxylipin profiles in mouse models of Wilson disease: New insights into early hepatic manifestations.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2024
    Article
  2. Article
  3. Sex-specific effects of neonatal oral sucrose treatment on growth and liver choline and glucocorticoid metabolism in adulthood.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
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

11 authors at 2 institutions in 1 country.

Raisa Syed1 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California , Davis, Sacramento, California.
Noreene M Shibata1 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California , Davis, Sacramento, California.
Kusum K Kharbanda2 Research Service, Veterans Affairs Nebraska-Western Iowa Health Care System , Omaha, Nebraska.
Ruijun J Su3 Department of Pathology and Laboratory Medicine, University of California , Davis, Sacramento, California.
Kristin Olson3 Department of Pathology and Laboratory Medicine, University of California , Davis, Sacramento, California.
Amy Yokoyama4 Division of Cardiovascular Medicine, Department of Internal Medicine, University of California , Davis, Davis, California.
John C Rutledge4 Division of Cardiovascular Medicine, Department of Internal Medicine, University of California , Davis, Davis, California.
Kenneth J Chmiel1 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California , Davis, Sacramento, California.
Kyoungmi Kim5 Division of Biostatistics, Department of Public Health Sciences, University of California , Davis, Davis, California.
Charles H Halsted1 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California , Davis, Sacramento, California.
Valentina Medici1 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California , Davis, Sacramento, California.
University of California, Davis · USVA Nebraska Western Iowa Health Care System · US

Funding

Brain Microvascular Determinants of Alzheimers DiseaseR01AG039094 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RUTLEDGE, JOHN CALVERT · 2010 to 2014
$2.1M
Role of lipid droplets in neurovascular inflammationR01AG045541 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RUTLEDGE, JOHN CALVERT, VILLABLANCA, AMPARO C · 2014 to 2018
$2.0M
Wilson Disease: Regulation of Steatosis by Methionine MetabolismK08DK084111 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MEDICI, VALENTINA · 2010 to 2014
$765k
Wilson Disease: Effect of High-Choline Feeding on Fetal and Offspring Mouse LiverR03DK099427 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MEDICI, VALENTINA · 2014 to 2015
$156k
Effect of Alcohol on Hepatic Creatine Biosynthesis: Role of Defective MethylationI01BX001155 · VA · OMAHA VA MEDICAL CENTER · PI KHARBANDA, KUSUM K. · 2012 to 2015
–
NIA NIH HHS R01AG039094NIA NIH HHS R01AG045541NIDDK NIH HHS K08DK084111NIDDK NIH HHS R03DK099427
6 · The paper itself

Abstract

backgroundPrevious studies indicated that nonpurified and purified commercially available control murine diets have different metabolic effects with potential consequences on hepatic methionine metabolism and liver histology.

methodsWe compared the metabolic and histological effects of commercial nonpurified (13% calories from fat; 57% calories from carbohydrates with 38 grams/kg of sucrose) and purified control diets (12% calories from fat; 69% calories from carbohydrates with ∼500 grams/kg of sucrose) with or without choline supplementation administered to C3H mice with normal lipid and methionine metabolism. Diets were started 2 weeks before mating, continued through pregnancy and lactation, and continued in offspring until 24 weeks of age when we collected plasma and liver tissue to study methionine and lipid metabolism.

resultsCompared to mice fed nonpurified diets, the liver/body weight ratio was significantly higher in mice fed either purified diet, which was associated with hepatic steatosis and inflammation. Plasma alanine aminotransferase levels were higher in mice receiving the purified diets. The hepatic S-adenosylmethionine (SAM)/S-adenosylhomocysteine (SAH) ratio was higher in female mice fed purified compared to nonpurified diet (4.6 ± 2 vs. 2.8 ± 1.9; P < 0.05). Choline supplementation was associated with improvement of some parameters of lipid and methionine metabolism in mice fed purified diets.

conclusionsStandard nonpurified and purified diets have significantly different effects on development of steatosis in control mice. These findings can help in development of animal models of fatty liver and in choosing appropriate laboratory control diets for control animals.

Indexed as

Lipid MetabolismAnimalsCholineDietDietary FatsDietary SucroseDietary SupplementsFatty LiverFeeding BehaviorFemaleLiverMethionineMiceMice, Inbred C3HS-AdenosylhomocysteineS-AdenosylmethionineCholineDietary FatsDietary SucroseMethionineS-AdenosylhomocysteineS-Adenosylmethionine

Identifiers

PMID26881897
PMCPMC4841906
OpenAlexW2287601820

What OpenQuestion holds

Textmetadata
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.