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机构地区:[1]济宁医学院附属医院麻醉科,山东省济宁市272029 [2]济宁医学院附属医院肾内科,山东省济宁市272029 [3]华中科技大学同济医学院协和医院麻醉科
出 处:《中华麻醉学杂志》2010年第7期881-883,共3页Chinese Journal of Anesthesiology
摘 要:目的探讨a-硫辛酸对体外循环诱发犬脑损伤的影响。方法健康杂种犬12只,雌雄不拘,体重13.5~17.5k,随机分为对照组(C组)和a-硫辛酸组(L组),每组6只。L组于CPB前即刻静脉注射a-硫辛酸50mg/kg,C组静脉注射等容量生理盐水。全心缺血60min,恢复灌注60min。分别于阻断升主动脉前(T0)、阻断升主动脉30、60min、再灌注30、60min(T1-4)时取股静脉血样,采用酶联免疫吸附双抗体夹心法测定血清,INF—a、S100β蛋白及神经元特异性烯醇化酶(NSE)的浓度。结果与T0时比较,两组,T1-4时血清TNF—a浓度、T2-4时NSE浓度、C组T1-4时S100β蛋白浓度升高(P〈0.05);与C组比较,L组T1~4时血清TNF-a、S100β蛋白浓度、T2-4时NSE浓度降低(P〈0.05)。C组血清TNF—a与S100β蛋白、NSE浓度成正相关(r=0.706,P〈0.01;r=0.81,P〈0.01)。结论a-硫辛酸可减轻体外循环诱发的犬脑损伤,与其抑制炎性反应有关。Objective To investigate the effect of a-lipoic acid on cerebral injury induced by cardiopulmonary bypass (CPB) in dogs. Methods Twelve adult healthy mengrel dogs of both sexes weighing 13.5-17.5 kg were randomly divided into control group (group C) and a-lopoic acid group (group L) (n = 6 each). In group L a-lipoic acid 50 mg/kg was injected iv immediately before CPB. The animals were anesthetized with intraperitoneal 2.5 % pentobarbital 25 mg/kg, intubated and mechanically ventilated. PaCO2 was maintained at 35-40 mm Hg. Femoral artery and vein were cannulated and Swan-Ganz catheter was inserted into pulmonary artery for MAP, CVP and CO monitoring and blood sampling. Blood samples were obtained immediately before aortic cross-clamping (T0 , baseline), at 30 and 60 min after aortic cross-clamping (T1,2) and 30 and 60 min after aortic unclamping (T3,4 ) for measurement of plasma concentrations of TNF-a, S100β protein and neuron-specific enolase (NSE). Results In group C CPB significantly increased plasma TNF-a, S100β protein and NSE concentrations as compared with the baseline values at TO . Pretreatment with a-lipoic acid significantly attenuated CPB-induced increase in plasma TNF-a, S100β protein and NSE concentrations in group L. Plasma S100β protein and NSE levels were positively correlated with plasma TNF-a level. Conclusion Pretreatment with a-lipoic acid is effective in attenuating CPB-induced inflammatory response and cerebral injury.
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