Evidence map›Paper›PMID 32439267›Full record

ArticleClinical nutrition (Edinburgh, Scotland)2021

Theaphenon E prevents fatty liver disease and increases CD4+ T cell survival in mice fed a high-fat diet.

Heidi Coia, Ning Ma, Yanqi Hou, Eva Permaul, Deborah L Berry, M Idalia Cruz, Evan Pannkuk, Michael Girgis, Zizhao Zhu, Yichen Lee and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical nutrition (Edinburgh, Scotland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Eating for immunity: how diet shapes our defenses.Current opinion in immunology · 2024
    Review
  5. The Role of CD4International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
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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 1 institution in 1 country.

Heidi CoiaDepartment of Biochemistry & Molecular Biology, Georgetown University Medical Center, Washington, DC 20057, USA. Electronic address: hgc10@georgetown.edu.
Ning MaDepartment of Biochemistry & Molecular Biology, Georgetown University Medical Center, Washington, DC 20057, USA. Electronic address: nm758@georgetown.edu.
Yanqi HouDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: hou_yanqi@163.com.
Eva PermaulDepartment of Pathology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: permaule@gmail.com.
Deborah L BerryDepartment of Pathology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: dlb82@georgetown.edu.
M Idalia CruzDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: cruzi@georgetown.edu.
Evan PannkukDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: elp44@georgetown.edu.
Michael GirgisDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: mg1773@georgetown.edu.
Zizhao ZhuDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: zz207@georgetown.edu.
Yichen LeeDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: yl285@georgetown.edu.
Olga RodriquezDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: Olga.Rodriquez@georgetown.edu.
Amrita CheemaDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: ack27@georgetown.edu.
Fung-Lung ChungDepartment of Biochemistry & Molecular Biology, Georgetown University Medical Center, Washington, DC 20057, USA; Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. Electronic address: flc6@georgetown.edu.
Georgetown University · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI Louis M Weiner · 1990 to 2026
$71.5M
Mechanisms of obesity-induced hepatocarcinogenesisR01CA190678 · NCI · GEORGETOWN UNIVERSITY · PI CHUNG, FUNG-LUNG, TANG, ERIC MOON-SHONG M. · 2015 to 2019
$1.8M
NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA190678
6 · The paper itself

Abstract

BACKGROUND &

aimsObesity is a major cause of non-alcoholic fatty liver disease (NAFLD). NAFLD is an epidemic affecting nearly 34% of the adult population in the US. As a chronic inflammatory disease, NAFLD influences the immune system by dysregulating T-cell activity. Remedies for the adverse effects on the immune system are urgently needed. We studied Theaphenon E (TE), a standardized formulation of green tea extract, on the adverse effects of NAFLD in C57BL/6J mice fed a high fat diet (HFD).

methodsMice received HFD, low fat diet (LFD) or HFD+2% TE for 35 weeks. Hepatic lipid accumulation, cell proliferation, apoptosis and CD4+T lymphocytes were measured throughout the bioassay. The hepatic composition of fatty acids was determined. The effects of epigallocatechin gallate (EGCG) metabolites on lipid accumulation in mouse and primary human liver cells were studied.

resultsUnlike mice receiving HFD, mice on HFD+2% TE maintained normal liver to body weight ratios with low levels of alanine and aspartate aminotransferase (ALT and AST). Hepatic lipid accumulation was observed in HFD mice, accompanied by increased proliferation, reduced apoptosis and loss of CD4+ T lymphocytes. TE significantly inhibited lipid accumulation, decreased proliferation, induced apoptosis and increased CD4+ T cell survival in HFD mice. It was found that the EGCG metabolite EGC-M3 reduced lipid accumulation in mouse and human hepatocytes. Linoleic acid showed the largest increase (2.5-fold) in livers of mice on a HFD and this increase was significantly suppressed by TE.

conclusionsLivers of HFD-fed mice showed lipid accumulation, increased proliferation, reduced apoptosis, elevated linoleic acid and loss of CD4+ T cells. TE effectively ameliorated all of these adverse effects.

Indexed as

AnimalsApoptosisCatechinCD4-Positive T-LymphocytesCell ProliferationDiet, Fat-RestrictedDiet, High-FatDisease Models, AnimalFatty AcidsHepatocytesHumansLinoleic AcidLipid MetabolismLiverMaleMiceCatechinepigallocatechin gallateFatty Acidsgreen tea extract polyphenone ELinoleic AcidCD4+T cellsLinoleic acidNon-alcoholic fatty liver diseasePrevention by green tea

Identifiers

PMID32439267
PMCPMC7609491
OpenAlexW3021550479

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.