Glutamate Excitotoxicity Mediates Neuronal Apoptosis After Hypothermic Circulatory Arrest

被引:40
作者
Tseng, Elaine E.
Brock, Malcolm V.
Lange, Mary S.
Troncoso, Juan C.
Blue, Mary E.
Lowenstein, Charles J.
Johnston, Michael V.
Baumgartner, William A.
机构
[1] Johns Hopkins Med Inst, Div Cardiac Surg, Baltimore, MD 21205 USA
[2] Kennedy Krieger Res Inst, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
FLOW CARDIOPULMONARY BYPASS; REDUCES NEUROLOGIC INJURY; INFANT HEART-SURGERY; NITRIC-OXIDE; NERVOUS-SYSTEM; PORCINE MODEL; DEATH; MECHANISM; CHILDREN; TRIAL;
D O I
10.1016/j.athoracsur.2009.10.059
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Prolonged hypothermic circulatory arrest results in neuronal cell death and neurologic injury. We have previously shown that hypothermic circulatory arrest causes both neuronal apoptosis and necrosis in a canine model. Inhibition of neuronal nitric oxide synthase reduced neuronal apoptosis, while glutamate receptor antagonism reduced necrosis in our model. This study was undertaken to determine whether glutamate receptor antagonism reduces nitric oxide formation and neuronal apoptosis after hypothermic circulatory arrest. Methods. Sixteen hound dogs underwent 2 hours of circulatory arrest at 18 degrees C and were sacrificed after 8 hours. Group 1 (n = 8) was treated with MK-801, 0.75 mg/kg intravenously prior to arrest followed by 75 mu g/kg/hour infusion. Group 2 dogs (n = 8) received vehicle only. Intracerebral levels of excitatory amino acids and citrulline, an equal coproduct of nitric oxide, were measured. Apoptosis, identified by hematoxylin and eosin staining and confirmed by electron microscopy, was blindly scored from 0 (normal) to 100 (severe injury), while nick-end labeling demonstrated DNA fragmentation. Results. Dogs in groups 1 and 2 had similar intracerebral levels of glutamate. However, MK-801 significantly reduced intracerebral glycine and citrulline levels compared with hypothermic circulatory arrest controls. The MK-801 significantly inhibited apoptosis (7.92 +/- 7.85 vs 62.08 +/- 6.28, group 1 vs group 2, p < 0.001). Conclusions. Our results showed that glutamate receptor antagonism significantly reduced nitric oxide formation and neuronal apoptosis. We provide evidence that glutamate excitotoxicity mediates neuronal apoptosis in addition to necrosis after hypothermic circulatory arrest. Clinical glutamate receptor antagonists may have therapeutic benefits in ameliorating both types of neurologic injury after hypothermic circulatory arrest. (Ann Thorac Surg 2010;89:440-5) (C) 2010 by The Society of Thoracic Surgeons
引用
收藏
页码:440 / 445
页数:6
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