AJP - Heart Calcium Transients and Cell-Sarcomere
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 296: H1920-H1925, 2009. First published April 17, 2009; doi:10.1152/ajpheart.01342.2008
0363-6135/09 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
296/6/H1920    most recent
01342.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (1)
Google Scholar
Right arrow Articles by Lund, D. D.
Right arrow Articles by Heistad, D. D.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lund, D. D.
Right arrow Articles by Heistad, D. D.

Protective effect of extracellular superoxide dismutase on endothelial function during aging

Donald D. Lund, Yi Chu, Jordan D. Miller, and Donald D. Heistad

Departments of Internal Medicine and Pharmacology and The Cardiovascular Center, University of Iowa Carver College of Medicine, and Veterans Affairs Medical Center, Iowa City, Iowa

Submitted 30 December 2008 ; accepted in final form 13 April 2009

Endothelial vasomotor function decreases with increasing age. Extracellular superoxide dismutase (ecSOD) protects against vascular dysfunction in several disease states. The purpose of this study was to determine whether endogenous ecSOD protects against endothelial dysfunction in old mice. Vasomotor function of the aorta was studied ex vivo in wild-type (ecSOD+/+) and ecSOD-deficient (ecSOD–/–) mice at 11 (adult) and 29 (old) mo of age. Maximal relaxation to acetylcholine (10–4 M) was impaired in vessels from adult ecSOD–/– mice [75 ± 3% (mean ± SE)] compared with wild-type mice (89 ± 2%, P < 0.05). Maximal relaxation to acetylcholine (10–4 M) was profoundly impaired in aorta from old ecSOD–/– mice (45 ± 5%) compared with wild-type mice (75 ± 4%, P < 0.05). There was a significant correlation between expression of ecSOD and maximal relaxation to acetylcholine in adult and old mice. Tempol (1 mM), a scavenger of superoxide, improved relaxation in response to acetylcholine (63 ± 8%) in old ecSOD–/– mice (P < 0.05), but not wild-type mice (75 ± 4%). Maximal relaxation to sodium nitroprusside was similar in aorta from adult and old wild-type and ecSOD–/– mice. Quantitative RT-PCR showed a decrease in mRNA levels of ecSOD and catalase in aorta of old mice and an increase in levels of TNF{alpha} and Nox-4 in aorta of old mice compared with adult mice. The findings support the hypothesis that impaired antioxidant mechanisms may contribute to cumulative increases in oxidative stress and impaired endothelial function in old mice. In conclusion, endogenous ecSOD plays an important role in protection against endothelial dysfunction during aging.

oxidative stress; antioxidants; vasomotor function; nitric oxide



Address for reprint requests and other correspondence: D. D. Heistad, Dept. of Internal Medicine, Univ. of Iowa, 200 Hawkins Dr., Iowa City, IA 52242-1081 (e-mail: donald-heistad{at}uiowa.edu)




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
T. Fukai
Extracellular SOD and aged blood vessels
Am J Physiol Heart Circ Physiol, July 1, 2009; 297(1): H10 - H12.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2009 by the American Physiological Society.