Effects of sesamin on aortic oxidative stress and endothelial dysfunction in deoxycorticosterone acetate-salt hypertensive rats

Biol Pharm Bull. 2003 Dec;26(12):1701-5. doi: 10.1248/bpb.26.1701.

Abstract

In the present study, we evaluated the relationship between the antihypertensive effect of sesamin, a lignan from sesame oil, and its antioxidative activity in deoxycorticosterone acetate (DOCA)-salt hypertensive rats. After a 5-week treatment period, systolic blood pressure was significantly elevated in normal diet-fed DOCA-salt animals compared with cases in sham-operated animals. Sesamin feeding, tempol (a superoxide dismutase mimetic) treatment or antihypertensive drugs combination (triple therapy; reserpine, hydralazine, hydrochlorothiazide) significantly suppressed the development of DOCA-salt-induced hypertension. Compared with sham-operated rats, the normal diet-fed DOCA-salt rats revealed marked increases in aortic superoxide (O(2)(-)) production. These increases in O(2)(-) production were significantly suppressed by sesamin feeding or tempol treatment, but not by triple therapy. Acetylcholine (Ach)-induced endothelium-dependent relaxation was markedly decreased in normal diet-fed DOCA-salt rats, compared with cases in sham-operated rats. Sesamin feeding and triple therapy significantly improved the DOCA-salt-induced impairment of endothelium-dependent relaxation. However, tempol treatment had no effect on the impaired vasodilator responses induced by DOCA-salt treatment. In DOCA-salt rats with or without sesamin feeding, systolic blood pressure significantly correlated with both aortic O(2)(-) production and endothelium-dependent vascular relaxation. These findings suggest that sesamin feeding inhibits the enhancement of aortic O(2)(-) production in DOCA-salt hypertensive rats, and this effect may contribute to the antihypertensive effect of sesamin. Sesamin feeding-induced improvement of endothelial dysfunction seems to result from the above antioxidative and antihypertensive effects.

Publication types

  • Comparative Study

MeSH terms

  • Acetylcholine / pharmacology
  • Administration, Oral
  • Animals
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / pharmacokinetics
  • Antihypertensive Agents / therapeutic use
  • Aorta / drug effects*
  • Aorta / metabolism
  • Blood Pressure / drug effects
  • Cyclic N-Oxides / administration & dosage
  • Desoxycorticosterone
  • Dioxoles / chemistry
  • Dioxoles / pharmacology
  • Dioxoles / therapeutic use*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Drug Therapy, Combination
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / pathology*
  • Endothelium, Vascular / physiology
  • Hypertension / chemically induced
  • Hypertension, Renovascular / drug therapy
  • Hypertension, Renovascular / physiopathology
  • Hypertension, Renovascular / prevention & control
  • Lignans / chemistry
  • Lignans / pharmacology
  • Lignans / therapeutic use*
  • Male
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / physiology
  • Oxidative Stress / drug effects*
  • Rats
  • Rats, Sprague-Dawley
  • Spin Labels
  • Superoxides / antagonists & inhibitors
  • Superoxides / metabolism
  • Vasodilation / drug effects
  • Vasodilation / physiology

Substances

  • Antihypertensive Agents
  • Cyclic N-Oxides
  • Dioxoles
  • Lignans
  • Spin Labels
  • Superoxides
  • Desoxycorticosterone
  • Acetylcholine
  • sesamin
  • tempol