Szabo L, Kovach A G, Babosa M, Greenberg J H, Revich M
Circ Shock. 1983;10(2):101-17.
In order to elucidate the possible role of noradrenergic hyperactivity in producing disturbances of cerebral circulation during hemorrhagic shock, the effect of prolonged norepinephrine infusion on local cerebral blood flow was studied in anesthetized and artificially ventilated rats. Intravenous infusion of 20 micrograms/(kg.min) norepinephrine for 2 hr produced circulatory shock characterized by progressive hypotension and acidosis. As a result, local cerebral blood flow, which was determined by autoradiography employing 14C-labeled iodoantipyrine in 79 different anatomical structures, decreased substantially in many areas. The most pronounced reductions were found in the regions supplied by the internal carotid artery, whereas the blood flow of the vertebral territory remained close to control. The blood supply of the cerebral cortex exhibited extreme heterogeneity with flow values below 0.10 ml/(min.gm). When either the intensity or the length of the infusion was reduced, no signs of circulatory breakdown could be observed. Variation of the infusion parameters demonstrated the dose-dependent nature of the cerebral blood flow response. Preinfusion blockade of alpha-receptors with 5 mg/kg phenoxybenzamine prevented the development of circulatory shock and reversed the decrease in cerebral blood flow induced by norepinephrine. The experimental results support the hypothesis that high concentration of norepinephrine in the vicinity of cerebral vessels produced by sympathetic hyperactivity might be an important factor in the etiology of blood flow deficiencies.
为了阐明去甲肾上腺素能亢进在出血性休克期间引起脑循环紊乱中可能发挥的作用,在麻醉并人工通气的大鼠中研究了长时间输注去甲肾上腺素对局部脑血流量的影响。以20微克/(千克·分钟)的剂量静脉输注去甲肾上腺素2小时,可产生以进行性低血压和酸中毒为特征的循环性休克。结果,通过使用14C标记的碘安替比林的放射自显影术在79个不同解剖结构中测定的局部脑血流量,在许多区域均显著下降。最明显的血流量减少出现在由颈内动脉供血的区域,而椎动脉供血区域的血流量仍接近对照值。大脑皮层的血液供应表现出极大的异质性,血流量值低于0.10毫升/(分钟·克)。当输注强度或时长降低时,未观察到循环衰竭的迹象。输注参数的变化表明脑血流量反应具有剂量依赖性。预先用5毫克/千克的酚苄明阻断α受体,可防止循环性休克的发生,并逆转去甲肾上腺素引起的脑血流量减少。实验结果支持这样的假说,即交感神经亢进导致脑血管附近去甲肾上腺素浓度升高,可能是血流量不足病因中的一个重要因素。