Role of vascular extracellular superoxide dismutase in hypertension.

Abstract

Previous studies indicate that superoxide is important in the modulation of blood pressure but have not specifically identified the cell types or organs involved. We created mice with loxP sites flanking the extracellular superoxide dismutase (SOD3) gene. These mice were crossed with mice expressing inducible Cre-recombinase driven by the smooth muscle myosin heavy chain promoter allowing tissue-specific deletion of SOD3. Deletion of SOD3 increased vascular superoxide and reduced vascular NO levels as detected by electron spin resonance. Despite these changes in NO and superoxide, we did not observe increases in vascular inflammation caused by angiotensin II. Moreover, deletion of vascular SOD3 did not augment hypertension in response to angiotensin II. In additional studies, we also deleted SOD3 from the circumventricular organs by intracerebroventricular injection of an adenovirus encoding Cre-recombinase. Although this raised blood pressure and augmented the hypertension caused by angiotensin II, these responses were not further increased by vascular deletion of SOD3. These data suggest that the extracellular superoxide dismutase in vascular smooth muscle is not involved in the genesis of angiotensin II-induced hypertension and further emphasize the role of central SOD3 in the modulation of blood pressure.

• Authors: Heinrich E Lob, Antony Vinh, Li Li, Yelena Blinder, Stefan Offermanns, David G Harrison
• Journal: Hypertension (Dallas, Tex. : 1979) (Hypertension) Vol. 58 Issue 2 Pg. 232-9 (Aug 2011) ISSN: 1524-4563 [Electronic] United States
• PMID: 21730294 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Angiotensin II
• Nitric Oxide
• Hydrogen Peroxide
• Sod3 protein, mouse
• Superoxide Dismutase

Topics

• Angiotensin II (pharmacology)
• Animals
• Aorta (metabolism, physiopathology)
• Blood Pressure (drug effects, physiology)
• Hydrogen Peroxide (metabolism)
• Hypertension (chemically induced, genetics, metabolism, physiopathology)
• Mice
• Mice, Transgenic
• Muscle, Smooth, Vascular (metabolism, physiopathology)
• Nitric Oxide (metabolism)
• Superoxide Dismutase (genetics, metabolism)