Sellke F W, Tofukuji M, Stamler A, Li J, Wang S Y
Division of Cardiothoracic Surgery, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Mass 02215, USA.
Circulation. 1997 Nov 4;96(9 Suppl):II-304-10.
The beta-adrenergic-cAMP pathway importantly regulates cerebral blood flow. Previous studies have found that normothermic cardiopulmonary bypass (CPB) is associated with reduced cerebral beta-adrenoceptor-mediated relaxation.
In order to examine the effects of hypothermic CPB on regulation of perfusion by the beta-adrenergic-cAMP pathway, pigs were placed on moderately (25 degrees C) or profoundly hypothermic (16 degrees C with 1 hour of circulatory arrest) or normothermic (37 degrees C) CPB for 2 hours. After normothermic perfusion for 15 minutes and separation from CPB, cerebral microvascular responses to the beta-adrenoceptor agonist isoproterenol (ISO), the adenylate cyclase activator forskolin, and the stable cAMP analogue 8-bromo-cAMP were examined in vitro in a pressurized, no-flow state. Baseline internal carotid artery blood flow was similar and unchanged after rewarming in the three experimental groups. However, ISO (100 micromol/L) elicited less relaxation after moderately hypothermic CPB (75+/-6%, P<.05 versus control, percent of U46619 induced precontraction) and profoundly hypothermic circulatory arrest (42+/-5%, P<.05) than in vessels from uninstrumented controls (91+/-2%) or after normothermic CPB (84+/-4%). The relaxation to forskolin was reduced after profoundly hypothermic circulatory arrest (83+/-3%, P<.05), but was similar in the other groups (92+/-2% control). Surprisingly, relaxation induced by 8-bromo-cAMP was markedly reduced after normothermic CPB, and this change was directly related to temperature during CPB. The intraluminal exposure of vessels to zymosan-induced complement activated serum had no effect on relaxation to ISO, while 2 hours of exposure of vessels to ISO caused a dose-dependent reduction in subsequent relaxation to ISO, but not to forskolin.
Moderately hypothermic CPB or PHCA desensitizes alpha-adrenoceptors more than normothermic CPB. This is likely due in part to the exposure of vessels to endogenous catecholamines during CPB. Thus, whereas baseline cerebral blood flow is similar after normothermic and hypothermic CPB, beta-adrenergic responses are markedly abnormal.
β-肾上腺素能-cAMP途径对脑血流量具有重要调节作用。既往研究发现,常温体外循环(CPB)与脑β-肾上腺素能受体介导的舒张功能降低有关。
为研究低温CPB对β-肾上腺素能-cAMP途径调节灌注的影响,将猪置于中度低温(25℃)、深度低温(16℃并循环停止1小时)或常温(37℃)CPB下2小时。在常温灌注15分钟并脱离CPB后,于体外在加压、无血流状态下检测脑微血管对β-肾上腺素能受体激动剂异丙肾上腺素(ISO)、腺苷酸环化酶激活剂福斯高林以及稳定的cAMP类似物8-溴-cAMP的反应。三个实验组复温后颈内动脉基线血流量相似且未发生变化。然而,与未插管对照血管(91±2%)或常温CPB后(84±4%)相比,中度低温CPB(75±6%,与对照相比P<0.05,U46619诱导预收缩的百分比)和深度低温循环停止后(42±5%,P<0.05),ISO(100μmol/L)引起的舒张作用较小。深度低温循环停止后对福斯高林的舒张反应降低(83±3%,P<0.05),但其他组相似(对照为92±2%)。令人惊讶的是,常温CPB后8-溴-cAMP诱导的舒张作用明显降低,且这种变化与CPB期间的温度直接相关。血管腔内暴露于酵母聚糖诱导的补体激活血清对ISO诱导的舒张无影响,而血管暴露于ISO 2小时会导致随后对ISO的舒张反应呈剂量依赖性降低,但对福斯高林无影响。
中度低温CPB或深度低温循环停止比常温CPB更易使α-肾上腺素能受体脱敏。这可能部分归因于CPB期间血管暴露于内源性儿茶酚胺。因此,尽管常温CPB和低温CPB后的基线脑血流量相似,但β-肾上腺素能反应明显异常。