Evidence map›Paper›PMID 8601628›Full record

ArticleThe Journal of clinical investigation1996

Genetic-dietary regulation of serum paraoxonase expression and its role in atherogenesis in a mouse model.

D M Shih, L Gu, S Hama, Y R Xia, M Navab, A M Fogelman, A J Lusis

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of clinical investigation, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
11.8field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 250 citations in OpenAlex.

  1. Serum paraoxonase 1 activity is decreased in thyroid dysfunction.Journal of endocrinological investigation · 2003
    Trial
  2. Article
  3. Article
  4. Antioxidants (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
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  9. Review
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  16. Article
  17. Review
  18. Article
  19. Article
  20. Human paraoxonase 2.EXCLI journal · 2010
    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

7 authors at 1 institution in 1 country.

D M ShihDepartment of Medicine, School of Medicine, University of California Los Angeles, 90095, USA.
L Gu
S Hama
Y R Xia
M Navab
A M Fogelman
A J Lusis
University of California, Los Angeles · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
UCLA TRAINING PROGRAM IN NUTRITION AND OBESITYT32DK007688 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HEBER, DAVID · 1992 to 2007
$1.3M
NHLBI NIH HHS HL-30568NIDDK NIH HHS 5T32DK07688-02
6 · The paper itself

Abstract

In an effort to identify genetic factors contributing to atherogenesis, we have studied inbred strains of mice that are susceptible (C57BL/6J) and resistant (C3H/HeJ) to diet-induced aortic fatty streak lesions. When maintained on a low-fat diet, HDL isolated from both strain C57BL/6J (B6) and C3H/HeJ (C3H) mice protect against LDL oxidation in a coculture model of the artery wall. However, when maintained on an atherogenic diet high in fat and cholesterol, the HDL isolated from B6 mice lose the capacity to protect, whereas HDL from C3H mice protect equally well. Associated with the loss in the ability of HDL to protect is a decrease in the activity of serum paraoxonase, a serum esterase carried on HDL that has previously been shown to protect against LDL oxidation in vitro. The levels of paraoxonase mRNA decreased in B6 mice upon challenge with the atherogenic diet but increased in C3H, indicating that paraoxonase production is under genetic control. In a set of recombinant inbred strains derived from the B6 and C3H parental strains, low paraoxonase mRNA levels segregated with aortic lesion development, supporting a role for paraoxonase in atherogenesis.

Indexed as

DietAmino Acid SequenceAnimalsArteriosclerosisAryldialkylphosphataseBase SequenceCloning, MolecularCrosses, GeneticDiet, AtherogenicDiet, Fat-RestrictedDisease Models, AnimalDNA, ComplementaryEsterasesFemaleGene ExpressionHumansAryldialkylphosphataseDNA, ComplementaryEsterasesLipoproteins, HDLLipoproteins, LDLRNA, Messenger

Identifiers

PMID8601628
PMCPMC507227
OpenAlexW2012639879

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.