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泮库溴铵和维库溴铵对大鼠离体心脏、肝脏、肾脏及膈肌中肌酸磷酸激酶的影响。

Effects of pancuronium and vecuronium on creatine phosphokinase in rat isolated heart, liver, kidney and diaphragm.

作者信息

Wali F A, Makinde V

机构信息

Respiratory and Anaesthetics Unit, Hospital for Sick Children, London, England.

出版信息

Gen Pharmacol. 1991;22(2):301-4. doi: 10.1016/0306-3623(91)90453-d.

Abstract
  1. The effects of two muscle relaxants, namely, pancuronium and vecuronium, on creatine phosphokinase (CPK) release from four different types of tissues, namely, heart, liver, kidney and diaphragm, were studied in the rat in vitro. 2. The total, neat and CPK levels (units/ml), released by muscle relaxants were measured using spectrophotometric determination at 340 nm. 3. The results showed that both muscle relaxants, in low concentrations, i.e. 0.34 or 0.32 microM, close to a clinical dose of 0.1 mg/kg, had no significant effect on CPK leakage in all four types of tissues studied. However, in concentrations 12-122 times clinical dose, the two muscle relaxants produced differential adverse effects in the tissues studied. 4. In most concentrations, pancuronium and vecuronium produced significant increases in the CPK release in the kidney and diaphragm. In contrast, pancuronium had no significant effect on CPK release in the liver and the lowest effect in the heart. Similar results were obtained with vecuronium. 5. The clinical relevance and/or implications of the present results are discussed and the results are compared to those previously reported by other workers in other preparations.
摘要
  1. 在大鼠体外实验中,研究了两种肌肉松弛剂,即泮库溴铵和维库溴铵,对四种不同类型组织,即心脏、肝脏、肾脏和膈肌中肌酸磷酸激酶(CPK)释放的影响。2. 使用分光光度法在340nm处测定肌肉松弛剂释放的总CPK水平、纯CPK水平(单位/毫升)。3. 结果表明,两种肌肉松弛剂在低浓度时,即0.34或0.32微摩尔,接近临床剂量0.1毫克/千克,对所研究的所有四种类型组织中的CPK泄漏均无显著影响。然而,在临床剂量的12 - 122倍浓度下,这两种肌肉松弛剂在所研究的组织中产生了不同的不良反应。4. 在大多数浓度下,泮库溴铵和维库溴铵使肾脏和膈肌中的CPK释放显著增加。相比之下,泮库溴铵对肝脏中的CPK释放无显著影响,对心脏中的影响最小。维库溴铵也得到了类似的结果。5. 讨论了本研究结果的临床相关性和/或意义,并将结果与其他研究人员在其他制剂中先前报道的结果进行了比较。

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