首页> 外文期刊>Journal of pharmaceutical sciences. >Hemodynamic profile in rabbits of fospropofol disodium injection relative to propofol emulsion following rapid bolus injection
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Hemodynamic profile in rabbits of fospropofol disodium injection relative to propofol emulsion following rapid bolus injection

机译:快速大剂量注射后,相对于丙泊酚乳剂,注射丙泊酚二钠的兔血流动力学特征

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摘要

The effects of aqueous fospropofol disodium (FP) and propofol emulsion (PE) on hemodynamics and sympathetic nerve activity in rabbits following bolus injection were evaluated. Barodenervated and neuraxis-intact rabbits received PE at 4 mg/kg (PE 4) or FP equal to 4 or 8 mg/kg propofol equivalents (FP 4 and FP 8, respectively) intravenously as a rapid bolus injection, and mean arterial pressure (MAP), heart rate (HR), and renal sympathetic nerve activity (RSNA) were recorded for 20 min. The plasma propofol pharmacokinetic behavior from FP and PE was evaluated to support the pharmacodynamic observations. In barodenervated animals, MAP and RSNA decreased significantly in all groups (PE 4 FP 8 FP 4). HR decreased only in the PE 4 group. The time for the maximum reduction of MAP was significantly longer with FP 8 compared with PE 4. MAP decreased, and RSNA and HR increased significantly in the neuraxis-intact animals (PE 4 FP 8 FP 4). The time for maximum reduction of MAP was essentially the same in all neuraxis-intact groups. Plasma propofol levels from FP were lower than those from PE in the first 4 min following administration. The results suggest that the tachycardia observed in humans following injection of FP is not a direct physiological effect of the agent.
机译:评估了大剂量注射后丙泊酚二钠水溶液(FP)和丙泊酚乳剂(PE)对家兔血液动力学和交感神经活动的影响。快速注射推注静脉注射速溶神经支原体和神经功能完好的兔子的PE为4 mg / kg(PE 4)或FP分别等于丙泊酚当量的4或8 mg / kg FP(FP 4和FP 8),平均动脉压(记录20分钟的MAP,心率(HR)和肾交感神经活动(RSNA)。评估了FP和PE的血浆丙泊酚药代动力学行为,以支持药效学观察。在无神经支配动物中,所有组的MAP和RSNA均显着降低(PE 4> FP 8> FP 4)。 HR仅在PE 4组中下降。与PE 4相比,FP 8可使MAP最大降低的时间明显更长。在神经轴完整的动物中,MAP降低,RSNA和HR显着增加(PE 4> FP 8> FP 4)。在所有神经完整的组中,最大程度降低MAP的时间基本相同。用药后头4分钟,FP的血浆丙泊酚水平低于PE。结果表明,注射FP后在人体内观察到的心动过速不是该药物的直接生理作用。

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