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Development of angiotensin II-induced abdominal aortic aneurysms is independent of catalase in mice.

Abstract
Chronic infusion of angiotensin II (AngII) into mice augments the development of abdominal aortic aneurysms (AAAs). Catalase is an important antioxidant enzyme in cellular peroxisome, and it physiologically maintains tissue and cellular redox homeostasis and thus plays a central role in defense against oxidative stress. The purpose of this study was to define whether deficiency of catalase influences AngII-induced AAAs. Male acatalasemic (C3H/AnLCsCs) mice and wild-type (C3H/AnLCsCs) mice (8-12 weeks old, N = 24 and 25, respectively) were fed a normal chow for 5 weeks. After 1 week of acclimtion, mice were infused subcutaneously with AngII (1000 ng·kg·min) by osmotic minipumps for 4 weeks. AngII increased systolic blood pressure equivalently in both groups. Acatalasemia had no effect on serum cholesterol concentrations. The body weight of acatalasemic mice was slightly greater than that of wild-type mice (P = 0.008). Although aortic catalase activity in acatalasemic mice was significantly low (P < 0.001), acatalasemia had no significant effect on the incidence of AngII-induced AAA formation (acatalasemia, 23%; wild, 21%), ex vivo measurement of maximal diameter of abdominal aorta (acatalasemia, 1.22 ± 0.29 mm; wild, 1.21 ± 0.17 mm), or aortic deposition of lipid peroxidation products such as 4-hydroxy-2-nonenal. The development of AngII-induced AAAs is independent of catalase.
AuthorsHaruhito A Uchida, Hitoshi Sugiyama, Keiichi Takiue, Yoko Kikumoto, Tatsuyuki Inoue, Hirofumi Makino
JournalJournal of cardiovascular pharmacology (J Cardiovasc Pharmacol) Vol. 58 Issue 6 Pg. 633-8 (Dec 2011) ISSN: 1533-4023 [Electronic] United States
PMID21885993 (Publication Type: Journal Article)
Chemical References
  • Aldehydes
  • Angiotensin II
  • Cholesterol
  • Catalase
  • 4-hydroxy-2-nonenal
Topics
  • Aldehydes (metabolism)
  • Angiotensin II (toxicity)
  • Animals
  • Aortic Aneurysm, Abdominal (chemically induced, pathology)
  • Blood Pressure (drug effects)
  • Body Weight
  • Catalase (genetics, metabolism)
  • Cholesterol (blood)
  • Lipid Peroxidation
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Knockout
  • Oxidative Stress

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