Evidence map›Paper›PMID 30151068›Full record

ArticleOxidative medicine and cellular longevity2018

Punicalagin Decreases Serum Glucose Levels and Increases PON1 Activity and HDL Anti-Inflammatory Values in Balb/c Mice Fed a High-Fat Diet.

Dana Atrahimovich, Abraham O Samson, Ali Khattib, Jacob Vaya, Soliman Khatib

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Linc-OIP5 working as a ceRNA of miR-616 promotes PON1 expression in HUEVC cells.International journal of clinical and experimental pathology · 2020
    Article
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Dana AtrahimovichDepartment of Oxidative Stress and Human Diseases, MIGAL-Galilee Research Institute, 11016 Kiryat Shmona, Israel.ORCID 0000-0003-4798-9824
Abraham O SamsonFaculty of Medicine in the Galilee, Bar-Ilan University, 1311502 Safed, Israel.ORCID 0000-0001-7436-3515
Ali KhattibDepartment of Oxidative Stress and Human Diseases, MIGAL-Galilee Research Institute, 11016 Kiryat Shmona, Israel.
Jacob VayaDepartment of Oxidative Stress and Human Diseases, MIGAL-Galilee Research Institute, 11016 Kiryat Shmona, Israel.
Soliman KhatibDepartment of Oxidative Stress and Human Diseases, MIGAL-Galilee Research Institute, 11016 Kiryat Shmona, Israel.ORCID 0000-0002-6762-2408
Migal - Galilee Technology Center · ILBar-Ilan University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyphenols are consumed daily in the human diet and are associated with reduced risk of a number of chronic diseases, including cancer, cardiovascular disease, and diabetes. Traditionally, the health benefits of polyphenols have been attributed to their antioxidant activity, but many studies might be hampered by oral administration and insignificant bioavailability. Rather than exerting a direct antioxidant effect, the mechanisms by which polyphenols express their beneficial effect seem to involve their interaction with proteins. The present study is aimed at broadening and confirming our recently published in vitro results showing that polyphenols may reduce atherosclerosis risk via interaction with proteins and lipoproteins related to atherosclerosis. The biological functions of punicalagin and quercetin in relation to glucose and lipid levels, paraoxonase 1 (PON1) activity, and inflammation were examined in vivo. Mice were fed a high-fat diet (HFD) for 12 weeks, and during the last 4 weeks, they received subcutaneous treatments via implanted minipumps, which released physiological concentrations of punicalagin, quercetin, or atorvastatin (as a positive control) daily into the serum. The HFD reduced serum PON1 activity, whereas punicalagin administration restored PON1 activity to the level of mice fed a normal diet. In addition, punicalagin significantly reduced glucose levels in HFD mice and improved HDL anti-inflammatory properties. In conclusion, beyond antioxidant activity, the mechanisms by which polyphenols exert their beneficial properties appear to involve their interaction with serum proteins that mediate HDL function and lipid-glucose state in the circulation.

Indexed as

AnimalsAryldialkylphosphataseBlood GlucoseDiet, High-FatHumansHydrolyzable TanninsLipoproteins, HDLMaleMiceMice, Inbred BALB CPolyphenolsAryldialkylphosphataseBlood GlucoseHydrolyzable TanninsLipoproteins, HDLPolyphenolsPON1 protein, mousepunicalagin

Identifiers

PMID30151068
PMCPMC6091419
OpenAlexW2887317281

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.