氢化可的松致糖madex对罗库溴铵所致神经肌肉阻滞的恢复作用:啮齿动物体内研究。

Anesthesia and pain medicine Pub Date : 2022-04-01 Epub Date: 2022-01-13 DOI:10.17085/apm.21076
Hey-Ran Choi, Hong-Seuk Yang, Jae-Moon Choi, Chungon Park, Junyong In, Yong Beom Kim
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引用次数: 0

摘要

背景:Sugammadex是氨基甾体神经肌肉阻滞剂的特异性拮抗剂,与客体分子1:1结合。Sugammadex还可以与化学结构中含有类固醇成分的其他药物结合。在这个体内实验中,我们研究了使用两种不同浓度的氢化可的松预暴露糖胺酮对罗库溴铵诱导的神经肌肉阻断的恢复差异。方法:取30只成年sd大鼠坐骨神经和胫前肌作为实验材料。坐骨神经采用四组(TOF)模式,每隔20 s进行间接超刺激。稳定15 min后,连续给予250 μg负荷剂量和125 μg加强剂量的罗库溴铵,直到确认TOF刺激的第一抽搐张力(T1)下降> 95%。将糖腺苷与等体积的三种不同原液(0.9%生理盐水、10 mg/ml氢化可的松、100 mg/ml氢化可的松)混合制备研究药物。同时测定T1和TOF比(TOFR)监测大鼠神经肌肉阻断后的恢复情况,直至T1恢复到> 95%,TOFR恢复到> 0.9。结果:糖madex与高浓度氢化可的松预混注射组T1、TOFR恢复进程组间差异有统计学意义(P < 0.050)。结论:当sugammadex仅预先暴露于高剂量的氢化可的松时,神经肌肉阻断的恢复延迟。当糖madex预先暴露于类固醇药物时,神经肌肉阻断的延迟恢复并不总是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of hydrocortisone-presensitized sugammadex on recovery from neuromuscular blockade induced by rocuronium: a rodent in vivo study.

Effects of hydrocortisone-presensitized sugammadex on recovery from neuromuscular blockade induced by rocuronium: a rodent in vivo study.

Effects of hydrocortisone-presensitized sugammadex on recovery from neuromuscular blockade induced by rocuronium: a rodent in vivo study.

Effects of hydrocortisone-presensitized sugammadex on recovery from neuromuscular blockade induced by rocuronium: a rodent in vivo study.

Background: Sugammadex is a specific antagonist of aminosteroidal neuromuscular blocking agents with 1:1 binding to guest molecules. Sugammadex can also bind to other drugs having a steroid component in its chemical structure. In this in vivo experiment, we investigated the differences in the recovery of rocuronium-induced neuromuscular blockade using sugammadex pre-exposed with two different concentrations of hydrocortisone.

Methods: The sciatic nerves and tibialis anterior muscles of 30 adult Sprague-Dawley rats were prepared for the experiment. The sciatic nerves were stimulated using a train-of-four (TOF) pattern with indirect supramaximal stimulation at 20 s intervals. After 15 min of stabilization, a 250 μg loading dose and 125 μg booster doses of rocuronium were serially administered until > 95% depression of the first twitch tension of TOF stimulation (T1) was confirmed. The study drugs were prepared by mixing sugamadex with the same volume of three different stock solutions (0.9% normal saline, 10 mg/ml hydrocortisone, and 100 mg/ ml hydrocortisone). The recovery of rats from neuromuscular blockade was monitored by assessing T1 and the TOF ratio (TOFR) simultaneously until T1 was recovered to > 95% and TOFR to > 0.9.

Results: In the group injected with sugammadex premixed with a high concentration of hydrocortisone, statistically significant intergroup differences were observed in the recovery progression of T1 and TOFR (P < 0.050).

Conclusions: When sugammadex was pre-exposed to a high dose of hydrocortisone only, recovery from neuromuscular blockade was delayed. Delayed recovery from neuromuscular blockade is not always plausible when sugammadex is pre-exposed to steroidal drugs.

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