Evidence map›Paper›PMID 23552499›Full record

ReviewAmerican journal of physiology. Regulatory, integrative and comparative physiology2013

Antioxidant-based therapies for angiotensin II-associated cardiovascular diseases.

Erin G Rosenbaugh, Krupa K Savalia, Devika S Manickam, Matthew C Zimmerman

Abstract readReview
In one paragraph

Review in American journal of physiology. Regulatory, integrative and comparative physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. HBiomedicines · 2023
    Article
  7. Review
  8. Toward Human Models of Cardiorenal SyndromeFrontiers in cardiovascular medicine · 2022
    Review
  9. Design and Antioxidant Properties of Bifunctional 2Molecules (Basel, Switzerland) · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Clinical Relevance and Role of Neuronal ATCirculation research · 2017
    Article
  18. Article
  19. Article
  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

4 authors.

Erin G RosenbaughDepartment of Cellular and Integrative Physiology, Nebraska Center for Nanomedicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Krupa K Savalia
Devika S Manickam
Matthew C Zimmerman

Funding

THE REDOX-MEDIATED REGULATION OF IRON-RESPONSIVE GENE EXPRESSION IN LIVERP20RR017675 · NCRR · UNIVERSITY OF NEBRASKA LINCOLN · PI GRASS, GREGOR · 2002 to 2011
$20.4M
Project 9 - Renal Drug Targeting for the Treatment of Lupus NephritisP20GM103480 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BRONICH, TATIANA K · 2012 to 2017
$13.3M
TARGETED NANOCARRIER FOR SIRNA DELIVERY TO TUMOR VASCULATUREP20RR021937 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KABANOV, ALEXANDER V · 2008 to 2011
$8.6M
Mitochondrial Redox Systems in Neurogenic HypertensionR01HL103942 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZIMMERMAN, MATTHEW C. · 2010 to 2014
$1.8M
Brain Delivery of Nanoformulated Superoxide DismutaseF31NS073398 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ROSENBAUGH, ERIN G · 2011 to 2013
$69k
NCRR NIH HHS P20 RR-017675NCRR NIH HHS P20 RR017675NCRR NIH HHS P20 RR021937NHLBI NIH HHS R01 HL-103942NHLBI NIH HHS R01 HL103942NIGMS NIH HHS P20 GM103480NIGMS NIH HHS P20GM103480NINDS NIH HHS F31 NS-073398
6 · The paper itself

Abstract

Cardiovascular diseases, including hypertension and heart failure, are associated with activation of the renin-angiotensin system (RAS) and increased circulating and tissue levels of ANG II, a primary effector peptide of the RAS. Through its actions on various cell types and organ systems, ANG II contributes to the pathogenesis of cardiovascular diseases by inducing cardiac and vascular hypertrophy, vasoconstriction, sodium and water reabsorption in kidneys, sympathoexcitation, and activation of the immune system. Cardiovascular research over the past 15-20 years has clearly implicated an important role for elevated levels of reactive oxygen species (ROS) in mediating these pathophysiological actions of ANG II. As such, the use of antioxidants, to reduce the elevated levels of ROS, as potential therapies for various ANG II-associated cardiovascular diseases has been intensely investigated. Although some antioxidant-based therapies have shown therapeutic impact in animal models of cardiovascular disease and in human patients, others have failed. In this review, we discuss the benefits and limitations of recent strategies, including gene therapy, dietary sources, low-molecular-weight free radical scavengers, polyethylene glycol conjugation, and nanomedicine-based technologies, which are designed to deliver antioxidants for the improved treatment of cardiovascular diseases. Although much work has been completed, additional research focusing on developing specific antioxidant molecules or proteins and identifying the ideal in vivo delivery system for such antioxidants is necessary before the use of antioxidant-based therapies for cardiovascular diseases become a clinical reality.

Indexed as

Angiotensin IIAnimalsAntioxidantsCardiovascular DiseasesDietGenetic TherapyHumansNanoparticlesReactive Oxygen SpeciesRenin-Angiotensin SystemAngiotensin IIAntioxidantsReactive Oxygen Speciesangiotensinantioxidantscardiovascular diseasefree radical scavengersoxidative stresstherapy

Identifiers

PMID23552499
PMCPMC3680755

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.