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Tyrosol attenuates ischemia-reperfusion-induced kidney injury via inhibition of inducible nitric oxide synthase.

Abstract
Tyrosol is a natural phenolic antioxidant compound. Oxidative stress represents one of the important mechanisms underlying ischemia-reperfusion-induced kidney injury. The aim of this study was to investigate the effect of tyrosol against ischemia-reperfusion-induced acute kidney injury. The left kidney of Sprague-Dawley rats was subjected to 45 min of ischemia followed by reperfusion for 6 h. Ischemia-reperfusion caused an increase in peroxynitrite formation and lipid peroxidation. The level of nitric oxide (NO) metabolites and the mRNA of inducible nitric oxide synthase (iNOS) were elevated in ischemia-reperfused kidneys. Administration of tyrosol (100 mg/kg body weight) to rats prior to the induction of ischemia significantly reduced peroxynitrite formation, lipid peroxidation, and the level of NO metabolites. Tyrosol administration also attenuated ischemia-reperfusion-induced NF-κB activation and iNOS expression. Such a treatment improved kidney function. Results suggest that tyrosol may have a protective effect against acute kidney injury through inhibition of iNOS-mediated oxidative stress.
AuthorsPengqi Wang, Qingjun Zhu, Nan Wu, Yaw L Siow, Harold Aukema, Karmin O
JournalJournal of agricultural and food chemistry (J Agric Food Chem) Vol. 61 Issue 15 Pg. 3669-75 (Apr 17 2013) ISSN: 1520-5118 [Electronic] United States
PMID23566115 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antioxidants
  • RNA, Messenger
  • 4-hydroxyphenylethanol
  • Nitric Oxide
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat
  • Phenylethyl Alcohol
Topics
  • Animals
  • Antioxidants (administration & dosage, therapeutic use)
  • Dose-Response Relationship, Drug
  • Down-Regulation (drug effects)
  • Injections, Intraperitoneal
  • Kidney (blood supply, drug effects, metabolism, physiopathology)
  • Lipid Peroxidation (drug effects)
  • Male
  • Nitric Oxide (metabolism)
  • Nitric Oxide Synthase Type II (genetics, metabolism)
  • Oxidative Stress (drug effects)
  • Phenylethyl Alcohol (administration & dosage, analogs & derivatives, therapeutic use)
  • RNA, Messenger (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury (metabolism, physiopathology, prevention & control)

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