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Angiotensin II type 1 receptor antagonist and angiotensin-converting enzyme inhibitor altered the activation of Cu/Zn-containing superoxide dismutase in the heart of stroke-prone spontaneously hypertensive rats.

Abstract
Although angiotensin II type 1 (AT1) receptor antagonists and angiotensin-converting enzyme (ACE) inhibitors are known to reduce both reactive oxygen species (ROS) generated by activated NAD(P)H oxidase and vascular remodeling in hypertension, the effects of AT1 receptor antagonists or ACE inhibitors on ROS-scavenging enzymes remain unclear. We hypothesized that AT1 receptor antagonists or ACE inhibitors may modulate vascular remodeling via superoxide dismutase (SOD) in hypertension. Male stroke-prone spontaneously hypertensive rats (SHRSP) were treated for 6 weeks with a vehicle, an AT1 receptor antagonist (E4177; 30 mg/kg/day), or an ACE inhibitor (cilazapril; 10 mg/kg/day). We evaluated protein expression using immunoblots, determined SOD activities with a spectrophotometric assay, and measured NAD(P)H oxidase activity by a luminescence assay. The two drugs showed equipotent effects on blood pressure, left ventricular hypertrophy and fibrosis, and endothelial NO synthase in the SHRSP hearts. The wall-to-lumen ratio of the intramyocardial arteries and the NAD(P)H oxidase essential subunit p22(phox) and its activity were significantly reduced, whereas Cu/Zu-containing SOD (Cu/ZnSOD) expression and activity were significantly increased in the SHRSP hearts. Furthermore, E4177 reduced vascular remodeling more than did cilazapril not only by reducing p22(phox) expression and NAD(P)H oxidase activity but also by upregulating the Cu/ ZnSOD expression and its activity in the SHRSP hearts. Thus, both the AT1 receptor antagonist and the ACE inhibitor inhibited vascular remodeling and reduced ROS in SHRSP via not only a reduction in NAD(P)H oxidase but also an upregulation of Cu/ZnSOD.
AuthorsMasakazu Tanaka, Seiji Umemoto, Shinji Kawahara, Makoto Kubo, Shinichi Itoh, Kyoko Umeji, Masunori Matsuzaki
JournalHypertension research : official journal of the Japanese Society of Hypertension (Hypertens Res) Vol. 28 Issue 1 Pg. 67-77 (Jan 2005) ISSN: 0916-9636 [Print] England
PMID15969257 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Imidazoles
  • Pyridines
  • Reactive Oxygen Species
  • 3-((2'-carboxybiphenyl-4-yl)methyl)-2-cyclopropyl-7-methyl-3H-imidazo(4,5-b)pyridine
  • Cilazapril
  • Superoxide Dismutase
Topics
  • Angiotensin II Type 1 Receptor Blockers (pharmacology)
  • Angiotensin-Converting Enzyme Inhibitors (pharmacology)
  • Animals
  • Blood Pressure (drug effects)
  • Cilazapril (pharmacology)
  • Heart Rate (drug effects)
  • Hypertension (drug therapy, metabolism)
  • Imidazoles (pharmacology)
  • Male
  • Myocardium (enzymology)
  • Oxidative Stress
  • Pyridines (pharmacology)
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Reactive Oxygen Species (metabolism)
  • Stroke (metabolism)
  • Superoxide Dismutase (metabolism)

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