LEUKEMIA INHIBITORY FACTOR AND TUMOR-NECROSIS-FACTOR INDUCE MANGANESE SUPEROXIDE-DISMUTASE AND PROTECT RABBIT HEARTS FROM REPERFUSION INJURY

被引:69
作者
NELSON, SK
WONG, GHW
MCCORD, JM
机构
[1] UNIV COLORADO, HLTH SCI CTR, DEPT BIOCHEM, DENVER, CO 80262 USA
[2] UNIV COLORADO, HLTH SCI CTR, DEPT MED, DENVER, CO 80262 USA
[3] GENENTECH INC, S SAN FRANCISCO, CA 94080 USA
关键词
LEUKEMIA INHIBITORY FACTOR (LIF); TUMOR NECROSIS FACTOR (TNF); ISCHEMIA; REPERFUSION; MANGANESE SUPEROXIDE DISMUTASE (MNSOD);
D O I
10.1016/S0022-2828(08)80021-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Leukemia inhibitory factor (LIF) and tumor necrosis factor (TNF) have been shown to protect animals from radiation, hyperoxia, and endotoxic shock. TNF is also known to induce the expression of manganese superoxide dismutase (MnSOD) in vitro and in vivo. We therefore examined the effects of these cytokines on reperfusion injury in the isolated rabbit heart model. Rabbits were injected intravenously with 10 mu g of either human TNF-alpha or lymphotoxin (TNF-beta), or murine TNF-alpha or murine LIF dissolved in saline, Control animals were injected with an equal volume of saline, After 24 h, hearts were isolated and perfused, Following an equilibration period, the hearts were subjected to 1 h ischemia and 1 h of reperfusion, All treated groups showed significant increases in percent recovery of developed tension (% preischemic) when compared to saline-treated control hearts. In addition there were significant decreases in lactate dehydrogenase release (LDH), accumulation of thiobarbituric acid reactive substances (TEARS), and accumulation of carbonyl proteins, These results correlate with increases in myocardial MnSOD activity, Thus, the protection from myocardial reperfusion injury seen in the pretreated group may be due to a mechanism that involves the induction of MnSOD.
引用
收藏
页码:223 / 229
页数:7
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