Harrison G J, Jordan L R, Willis R J
Rotary Centre for Cardiovascular Research, Griffith University, Brisbane, Australia.
Can J Cardiol. 1994 Oct;10(8):843-9.
To examine the effect of hydrogen peroxide on the function and ultrastructure of cardiac muscle and the coronary vasculature in an isovolumic rat heart preparation perfused at constant flow.
Ventricular function was monitored via a balloon placed in the left ventricle and the response of the coronary vessels to vasodilators was assessed in hearts arrested with 35 mM potassium and treated with 5 microM phenylephrine to contract the coronary resistance vessels. Changes in coronary perfusion pressure reflect changes in resistance vessel tone. SETTING/ANIMALS: This experimental study consisted of 14 heart preparations, six control and eight treated hearts.
Hydrogen peroxide was included in the perfusate at a final concentration of 250 microM for 20 mins.
Hydrogen peroxide reduced rate-pressure product by 42%, caused a fivefold increase in end-diastolic pressure and increased coronary perfusion pressure by 33%. Also, the response of the coronary vasculature to the endothelium-dependent vasodilator, histamine, and endothelium-independent vasodilator, sodium nitrite, was decreased by 55% and 53%, respectively. Electron microscopy of hydrogen peroxide-treated hearts showed damage to both capillaries and arterioles. Endothelial cells were distorted and contained pinocytotic vesicles, endothelial cell junctions were disrupted and blood vessels were detached from surrounding tissue. A comparatively small amount of injury was seen in the myocyte population.
The greater amount of ultrastructural damage seen in blood vessels compared with cardiac muscle suggests that the smooth muscle and endothelial cells of the vasculature are more susceptible to oxidant injury than the myocytes.
在恒流灌注的等容大鼠心脏标本中,研究过氧化氢对心肌功能、超微结构以及冠状血管的影响。
通过置于左心室内的球囊监测心室功能,并在使用35 mM钾使心脏停搏且用5 microM去氧肾上腺素使冠状阻力血管收缩的心脏中,评估冠状血管对血管舒张剂的反应。冠状灌注压的变化反映阻力血管张力的变化。设置/动物:本实验研究包括14个心脏标本,6个对照心脏和8个处理过的心脏。
在灌注液中加入过氧化氢,终浓度为250 microM,持续20分钟。
过氧化氢使心率-血压乘积降低42%,使舒张末期压力增加五倍,并使冠状灌注压升高33%。此外,冠状血管对内皮依赖性血管舒张剂组胺和非内皮依赖性血管舒张剂亚硝酸钠的反应分别降低了55%和53%。对用过氧化氢处理的心脏进行电子显微镜检查显示,毛细血管和小动脉均有损伤。内皮细胞扭曲,含有吞饮小泡,内皮细胞连接中断,血管与周围组织分离。在心肌细胞群体中观察到相对少量的损伤。
与心肌相比,血管中观察到的超微结构损伤更多,这表明血管的平滑肌和内皮细胞比心肌细胞更容易受到氧化损伤。