Abstract | BACKGROUND: METHODS: RESULTS:
Myocardial infarction developed and plasma CK and LDH activities were significantly increased in I/R group compared with those in control group, but SO2 preconditioning significantly reduced myocardial infarct size, and plasma CK and LDH activities. SO2 preconditioning successfully increased plasma SOD, GSH and GSH-Px levels and myocardial SOD1 protein expression, but decreased MDA level in rats of I/R group. Compared with controls, the myocardial H2S level and CSE expression were decreased after I/R, but myocardial NO level and iNOS expression were increased. With the treatment of SO2, myocardial H2S level and CSE expression were increased, but myocardial NO level and iNOS expression were decreased compared with those in I/R group. CONCLUSIONS: SO2 preconditioning could significantly reduce I/R-induced myocardial injury in vivo in association with increased myocardial antioxidative capacity, upregulated myocardial H2S/CSE pathway but downregulated NO/iNOS pathway.
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Authors | Hong fang Jin, Yuan Wang, Xin bao Wang, Yan Sun, Chao shu Tang, Jun bao Du |
Journal | Nitric oxide : biology and chemistry
(Nitric Oxide)
Vol. 32
Pg. 56-61
(Aug 01 2013)
ISSN: 1089-8611 [Electronic] United States |
PMID | 23629152
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier Inc. All rights reserved. |
Chemical References |
- Antioxidants
- Sulfur Dioxide
- Nitric Oxide
- L-Lactate Dehydrogenase
- Nitric Oxide Synthase Type II
- Nos2 protein, rat
- Sod1 protein, rat
- Superoxide Dismutase
- Superoxide Dismutase-1
- Creatine Kinase
- Cystathionine gamma-Lyase
- Glutathione
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Topics |
- Animals
- Antioxidants
(metabolism)
- Creatine Kinase
(metabolism)
- Cystathionine gamma-Lyase
(metabolism)
- Glutathione
(metabolism)
- Ischemic Preconditioning, Myocardial
(methods)
- L-Lactate Dehydrogenase
(metabolism)
- Male
- Myocardial Infarction
(metabolism)
- Myocardial Reperfusion Injury
(drug therapy, metabolism)
- Nitric Oxide
(metabolism)
- Nitric Oxide Synthase Type II
(metabolism)
- Oxidative Stress
(drug effects)
- Rats
- Rats, Wistar
- Sulfur Dioxide
(pharmacology)
- Superoxide Dismutase
(metabolism)
- Superoxide Dismutase-1
|