Kidney Res Clin Pract.  2012 Dec;31(4):227-233.

Endothelium-dependent vasodilation by ferulic acid in aorta from chronic renal hypertensive rats

Affiliations
  • 1Department of Physiology, College of Medicine, Chosun University, Gwangju, Korea. chyum@chosun.ac.kr
  • 2Department of Psychiatry, College of Medicine, Chosun University, Gwangju, Korea.
  • 3Department of Internal Medicine, College of Medicine, Chosun University, Gwangju, Korea.

Abstract

BACKGROUND
Ferulic acid (FA) is a naturally occurring nutritional compound. Although it has been shown to have antihypertensive effects, its effects on vascular function have not been intensively established. The aim of this study was to assess the vasoreactivity of FA in chronic two-kidney, one-clip (2K1C) renal hypertensive rats.
METHODS
Hypertension was induced in 2K1C rats by clipping the left renal artery and age-matched rats that received a sham treatment served as a control. Thoracic aortas were mounted in tissue baths to measure isometric tension. The effects of FA on vasodilatory responses were evaluated based on contractile responses induced by phenylephrine in the aortic rings obtained from both 2K1C and sham rats. Basal nitric oxide (NO) bioavailability in the aorta was determined by the contractile response induced by NO synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME).
RESULTS
FA induced concentration-dependent relaxation responses which were greater in 2K1C hypertensive rats than in sham-clipped control rats. This relaxation induced by FA was partially blocked by the removal of endothelium or by pretreating with L-NAME. L-NAME-induced contractile responses were augmented by FA in 2K1C rats, while no significant differences were noted in sham rats. FA improved acetylcholine-induced endothelium-dependent vasodilation in 2K1C rats, but not in sham rats. The simultaneous addition of hydroxyhydroquinone significantly inhibited the increase in acetylcholine-induced vasodilation by FA.
CONCLUSION
These results suggest that FA restores endothelial function by altering the bioavailability of NO in 2K1C hypertensive rats. The results explain, in part, the mechanism underlying the vascular effects of FA in chronic renal hypertension.

Keyword

Endothelium; Ferulic acid; Renal hypertension; Vasodilation

MeSH Terms

Animals
Aorta
Aorta, Thoracic
Baths
Biological Availability
Coumaric Acids
Endothelium
Hydroquinones
Hypertension
Hypertension, Renal
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitric Oxide Synthase
Phenylephrine
Placebos
Rats
Relaxation
Renal Artery
Salicylamides
Vasodilation
Coumaric Acids
Hydroquinones
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitric Oxide Synthase
Phenylephrine
Placebos
Salicylamides
Full Text Links
  • KRCP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr