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失血性休克对大鼠体内吗啡药代动力学及镇痛效果的影响。

The influence of hemorrhagic shock on the pharmacokinetics and the analgesic effect of morphine in the rat.

作者信息

De Paepe P, Belpaire F M, Rosseel M T, Buylaert W A

机构信息

Heymans Institute of Pharmacology, University of Gent, Medical School, Belgium.

出版信息

Fundam Clin Pharmacol. 1998;12(6):624-30. doi: 10.1111/j.1472-8206.1998.tb00996.x.

Abstract

The influence of hemorrhagic shock (removal of 30% of the blood volume) on the pharmacokinetics and the analgesic effect of morphine was investigated in conscious rats. Plasma concentrations of morphine after a bolus injection (5 mg/kg) are higher in the shock animals, which is attributed to a small decrease in clearance (-22%; P > 0.05) and a significant decrease in distribution volume (-33%; P < 0.05) of the drug. The areas under the plasma concentration-time curve of the metabolite morphine-3-glucuronide (M3G) are significantly higher (+237%; P < 0.01) in the shock rats, which is probably explained by a decreased distribution and renal excretion. The analgesic effect of morphine was evaluated using the tail-flick test during a continuous infusion (10 mg/kg/h) with measurement of the plasma concentrations of morphine and M3G. Data from these experiments show higher plasma concentrations of morphine (+33%; P < 0.05) and M3G (+66%; P > 0.05) during shock, and a significantly increased analgesic effect (+43%; P < 0.05). Our data suggest that the increased analgesic effect of morphine during hemorrhagic shock can most likely be explained by pharmacokinetic changes resulting in higher morphine concentrations.

摘要

在清醒大鼠中研究了失血性休克(失血30%血容量)对吗啡药代动力学及镇痛效果的影响。推注(5毫克/千克)吗啡后,休克动物的血浆吗啡浓度较高,这归因于药物清除率略有下降(-22%;P>0.05)和分布容积显著下降(-33%;P<0.05)。休克大鼠中代谢产物吗啡-3-葡萄糖醛酸苷(M3G)的血浆浓度-时间曲线下面积显著更高(+237%;P<0.01),这可能是由于分布和肾脏排泄减少所致。在持续输注(10毫克/千克/小时)期间,使用甩尾试验评估吗啡的镇痛效果,并测量吗啡和M3G的血浆浓度。这些实验数据显示,休克期间吗啡(+33%;P<0.05)和M3G(+66%;P>0.05)的血浆浓度更高,镇痛效果显著增强(+43%;P<0.05)。我们的数据表明,失血性休克期间吗啡镇痛效果增强很可能是由药代动力学变化导致吗啡浓度升高所致。

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