Evidence map›Paper›PMID 29226146›Full record

ArticleBioMed research international2017

Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice.

Shadi Hamoud, Rabia Shekh Muhammad, Niroz Abu-Saleh, Ahmad Hassan, Yaniv Zohar, Tony Hayek

Abstract read
In one paragraph

Article in BioMed research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Endothelial glycocalyx in retina, hyperglycemia, and diabetic retinopathy.American journal of physiology. Cell physiology · 2023
    Review
  5. Review
  6. Heparanase Inhibition Prevents Liver Steatosis in EJournal of clinical medicine · 2022
    Article
  7. Review
  8. Heparanase and the hallmarks of cancer.Journal of translational medicine · 2020
    Review
  9. Serum Heparanase Level Is Decreased in Stable Coronary Artery Disease.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2019
    Article
  10. Article
  11. Article
  12. The heparan sulfate proteoglycan grip on hyperlipidemia and atherosclerosis.Matrix biology : journal of the International Society for Matrix Biology · 2018
    Review
  13. Article
  14. 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

6 authors.

Shadi HamoudInternal Medicine E Department, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.ORCID 0000-0003-1405-239X
Rabia Shekh MuhammadInternal Medicine A Department, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Niroz Abu-SalehLipid Research Laboratory, Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Ahmad HassanInternal Medicine A Department, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Yaniv ZoharPathology Department, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Tony HayekInternal Medicine E Department, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtherosclerosis is a multifactorial process. Emerging evidence highlights a role of the enzyme heparanase in various disease states, including atherosclerosis formation and progression.

objectiveThe aim of the study was to investigate the effect of heparanase inhibition on blood pressure, blood glucose levels, and oxidative stress in apoE-/- mice.

methodsMale apoE-/- mice were divided into two groups: one treated by the heparanase inhibitor PG545, administered intraperitoneally weekly for seven weeks, and the other serving as control group (injected with saline). Blood pressure was measured a day before sacrificing the animals. Serum glucose levels and lipid profile were measured. Assessment of oxidative stress was performed as well.

resultsPG545 significantly lowered blood pressure and serum glucose levels in treated mice. It also caused significant reduction of the serum oxidative stress. For safety concerns, liver enzymes were assessed, and PG545 caused significant elevation only of alanine aminotransferase, but not of the other hepatic enzymes.

conclusionHeparanase inhibition by PG545 caused marked reduction of blood pressure, serum glucose levels, and oxidative stress in apolipoprotein E deficient mice, possibly via direct favorable metabolic and hemodynamic changes caused by the inhibitor. Possible hepatotoxic and weight wasting effects are subject for future investigation.

Indexed as

AnimalsApolipoproteins EAtherosclerosisBlood GlucoseBlood PressureGlucoseGlucuronidaseHeparanaseLipidsLiverMaleMiceMice, KnockoutOxidative StressSaponinsApolipoproteins EBlood GlucoseGlucoseGlucuronidaseHeparanaseLipidsPG 545Saponins

Identifiers

PMID29226146
PMCPMC5684525

What OpenQuestion holds

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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.