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A Food-Derived Flavonoid Luteolin Protects against Angiotensin II-Induced Cardiac Remodeling.

Abstract
Oxidative stress has been implicated in cardiac remodeling (cardiac fibrosis and hypertrophy), which impairs cardiac function and metabolism; therefore, it is anticipated antioxidative compounds will have protective properties against cardiac remodeling. Luteolin (3',4',5,7-tetrahydroxyflavone), a widely distributed flavonoid found in many herbal extracts including celery, green pepper, perilla leaves and seeds, and chamomile, is a known to be a potent antioxidant and was previously demonstrated to exert an antifibrotic effect in the lungs and the liver. In this study, we clearly demonstrate that oral pretreatment with the higher-luteolin diet (0.035% (wt/wt)) protected against cardiac fibrosis and hypertrophy as well as a hyperoxidative state in Ang II-infused rats. In cardiac tissue, increased gene expression levels of TGFβ1, CTGF, Nox2, Nox4, ANP, and BNP induced by Ang II were restored by oral pretreatment of this high-luteolin diet. In cultured rat cardiac fibroblasts, H2O2-induced TGFβ1 expression and the phosphorylation of JNK were suppressed by luteolin pretreatment. In conclusion, food-derived luteolin has protective actions against Ang II-induced cardiac remodeling, which could be mediated through attenuation of oxidative stress.
AuthorsAtsuko Nakayama, Hiroyuki Morita, Tomoko Nakao, Toshihiro Yamaguchi, Tomokazu Sumida, Yuichi Ikeda, Hidetoshi Kumagai, Yoshihiro Motozawa, Tsukasa Takahashi, Atsushi Imaizumi, Tadashi Hashimoto, Ryozo Nagai, Issei Komuro
JournalPloS one (PLoS One) Vol. 10 Issue 9 Pg. e0137106 ( 2015) ISSN: 1932-6203 [Electronic] United States
PMID26327560 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antioxidants
  • CCN2 protein, rat
  • Flavonoids
  • Transforming Growth Factor beta1
  • Angiotensin II
  • Connective Tissue Growth Factor
  • Atrial Natriuretic Factor
  • Hydrogen Peroxide
  • Luteolin
Topics
  • Angiotensin II (pharmacology)
  • Animals
  • Antioxidants (pharmacology)
  • Atrial Natriuretic Factor (metabolism)
  • Connective Tissue Growth Factor (metabolism)
  • Diet
  • Fibroblasts (drug effects, metabolism)
  • Fibrosis (drug therapy, metabolism)
  • Flavonoids (pharmacology)
  • Food
  • Heart (drug effects)
  • Hydrogen Peroxide (pharmacology)
  • Hypertrophy (drug therapy, metabolism)
  • Luteolin (pharmacology)
  • Male
  • Myocardium (metabolism)
  • Oxidative Stress (drug effects)
  • Phosphorylation (drug effects)
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction (drug effects)
  • Transforming Growth Factor beta1 (metabolism)
  • Ventricular Remodeling (drug effects)

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