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大鼠体内由沙拉新或硝普钠诱导的血流改变。

Blood flow alteration induced by saralasin or sodium nitroprusside in rats.

作者信息

Miller E D, Delaney T J

出版信息

Anesthesiology. 1981 Mar;54(3):199-203. doi: 10.1097/00000542-198103000-00005.

Abstract

The radioactive microsphere technique was used to investigate the distribution of blood flow during halothane anesthesia when either sodium nitroprusside (SNP) or saralasin, a competitive inhibitor of angiotensin II, was infused. Seventeen fasted male Wistar rats were anesthetized with halothane and received either saralasin (n = 6) or SNP (n = 11) to decrease mean arterial pressure 20 torr. Cardiac output was unchanged with SNP, but blood flow decreased 23 per cent to the brain, and 25 per cent to the kidney, while splanchnic flow increased 19 per cent (P less than .05). There were 37 per cent less microspheres present in the lung after drug treatment. Saralasin did not alter cardiac output or flow to other organs but did cause a 49 per cent decrease in the number of microspheres found in the lung after drug treatment. An additional group of rats first received SNP, and then saralasin. This combination was not well tolerated, resulting in lethal hypotension and a mortality of 60 per cent. In the thirteen animals which were able to complete the protocol, increases in blood flow to the heart, kidney and splanchnic circulation were seen while brain flow decreased (P less than .05). The number of microspheres in the lung also decreased after combined therapy. These studies demonstrate the differential effects of SNP and saralasin in lowering blood pressure. The use of combined drug treatment, when tolerated, may improve organ perfusion.

摘要

采用放射性微球技术,研究在氟烷麻醉期间输注硝普钠(SNP)或血管紧张素II竞争性抑制剂沙拉新时的血流分布情况。17只禁食雄性Wistar大鼠用氟烷麻醉,分别给予沙拉新(n = 6)或SNP(n = 11),使平均动脉压降低20托。SNP使心输出量不变,但脑血流量减少23%,肾血流量减少25%,而内脏血流量增加19%(P<0.05)。药物治疗后肺内微球数量减少37%。沙拉新不改变心输出量或其他器官的血流量,但药物治疗后肺内微球数量减少49%。另一组大鼠先给予SNP,然后给予沙拉新。这种联合用药耐受性差,导致致命性低血压,死亡率为60%。在能够完成实验方案的13只动物中,心脏、肾脏和内脏循环血流量增加,而脑血流量减少(P<0.05)。联合治疗后肺内微球数量也减少。这些研究证明了SNP和沙拉新在降低血压方面的不同作用。当耐受性良好时,联合药物治疗可能改善器官灌注。

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