Abstract | PURPOSE:
Ethyl pyruvate has anti-inflammatory properties and protects organs from ischemia/reperfusion (I/R)-induced tissue injury. The aim of this study was to determine whether ethyl pyruvate decreases the inflammatory response after regional I/R injury and whether ethyl pyruvate protects against delayed regional I/R injury in an in vivo rat heart model after a 24 hours reperfusion. MATERIALS AND METHODS: RESULTS: At 2 hours after I/R injury, ethyl pyruvate attenuated I/R-induced nuclear factor κB translocation and reduced myeloperoxidase activity in myocardium. The plasma circulating levels of inflammatory cytokines decreased significantly in the ethyl pyruvate-treated group. At 24 hours after I/R injury, ethyl pyruvate significantly improved cardiac function and reduced infarct size after regional I/R injury. CONCLUSION:
Ethyl pyruvate has the ability to inhibit neutrophil activation, inflammatory cytokine release, and nuclear factor κB translocation. Ethyl pyruvate is associated with a delayed myocardial protective effect after regional I/R injury in an in vivo rat heart model.
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Authors | In-Seok Jang, Mi-Young Park, Il-Woo Shin, Ju-Tae Sohn, Heon-Keun Lee, Young-Kyun Chung |
Journal | Yonsei medical journal
(Yonsei Med J)
Vol. 51
Issue 6
Pg. 838-44
(Nov 2010)
ISSN: 1976-2437 [Electronic] Korea (South) |
PMID | 20879048
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Inflammatory Agents
- NF-kappa B
- Pyruvates
- ethyl pyruvate
- Peroxidase
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Topics |
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Cell Nucleus
(metabolism)
- Cytoplasm
(metabolism)
- Heart
(physiopathology)
- Inflammation
- Male
- Myocardial Infarction
(prevention & control)
- Myocardium
(metabolism)
- NF-kappa B
(metabolism)
- Peroxidase
(metabolism)
- Pyruvates
(pharmacology)
- Rats
- Rats, Sprague-Dawley
- Reperfusion Injury
(drug therapy, metabolism)
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