Effects of HMGB1 on Ischemia-Reperfusion Injury in the Rat Heart

Background Coronary ischemia-reperfusion (I/R) injury causes cardiomyocyte necrosis in a multi-step process that includes an inflammatory reaction. A recent study has suggested that high-mobility group box 1 (HMGB1) is a late mediator of lethal sepsis and an early mediator of inflammation and necros...

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Veröffentlicht in:Circulation Journal 2008, Vol.72(7), pp.1178-1184
Hauptverfasser: Oozawa, Susumu, Mori, Shuji, Kanke, Toru, Takahashi, Hideo, Liu, Keyue, Tomono, Yasuko, Asanuma, Masato, Miyazaki, Ikuko, Nishibori, Masahiro, Sano, Shunji
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Sprache:eng
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Zusammenfassung:Background Coronary ischemia-reperfusion (I/R) injury causes cardiomyocyte necrosis in a multi-step process that includes an inflammatory reaction. A recent study has suggested that high-mobility group box 1 (HMGB1) is a late mediator of lethal sepsis and an early mediator of inflammation and necrosis following I/R injury. In the present study a neutralizing monoclonal antibody (mAb) for HMGB1 was used to clarify the role of HMGB1 in cardiac I/R injury. Methods and Results Rats underwent 30 min of left coronary artery occlusion followed by 60 min reperfusion. An intravenous injection of anti-HMGB1 mAb or control IgG was administered just before reperfusion. The infarct size was enlarged in the anti-HMGB1 mAb group in comparison with the control group (p
ISSN:1346-9843
1347-4820
DOI:10.1253/circj.72.1178