PPARs: Protectors or Opponents of Myocardial Function?

Joint Authors

Pol, Christine J.
Lieu, Melissa
Drosatos, Konstantinos

Source

PPAR Research

Issue

Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-19, 19 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2015-12-02

Country of Publication

Egypt

No. of Pages

19

Main Subjects

Biology

Abstract EN

Over 5 million people in the United States suffer from the complications of heart failure (HF), which is a rapidly expanding health complication.

Disorders that contribute to HF include ischemic cardiac disease, cardiomyopathies, and hypertension.

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptor family.

There are three PPAR isoforms: PPARα, PPARγ, and PPARδ.

They can be activated by endogenous ligands, such as fatty acids, as well as by pharmacologic agents.

Activators of PPARs are used for treating several metabolic complications, such as diabetes and hyperlipidemia that are directly or indirectly associated with HF.

However, some of these drugs have adverse effects that compromise cardiac function.

This review article aims to summarize the current basic and clinical research findings of the beneficial or detrimental effects of PPAR biology on myocardial function.

American Psychological Association (APA)

Pol, Christine J.& Lieu, Melissa& Drosatos, Konstantinos. 2015. PPARs: Protectors or Opponents of Myocardial Function?. PPAR Research،Vol. 2015, no. 2015, pp.1-19.
https://search.emarefa.net/detail/BIM-1075970

Modern Language Association (MLA)

Pol, Christine J.…[et al.]. PPARs: Protectors or Opponents of Myocardial Function?. PPAR Research No. 2015 (2015), pp.1-19.
https://search.emarefa.net/detail/BIM-1075970

American Medical Association (AMA)

Pol, Christine J.& Lieu, Melissa& Drosatos, Konstantinos. PPARs: Protectors or Opponents of Myocardial Function?. PPAR Research. 2015. Vol. 2015, no. 2015, pp.1-19.
https://search.emarefa.net/detail/BIM-1075970

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1075970