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Effect of protracted dexamethasone exposure and its withdrawal on rocuronium-induced neuromuscular blockade and sugammadex reversal: an ex vivo rat study

机译:长期地塞米松暴露及其戒断对罗库溴铵诱导的神经肌肉阻滞和舒马葡糖逆转的影响:离体大鼠研究

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摘要

Studies have reported that protracted dexamethasone treatment induces resistance to nondepolarizing neuromuscular blocking agents (NMBAs) and the association with nicotinic acetylcholine receptors in the diaphragm of rats. Here, we investigated the effect of protracted dexamethasone administration on the sensitivity to rocuronium and the recovery profile when reversed by sugammadex; additionally, we observed the recovery period of pharmacodynamic change after withdrawal. Sprague-Dawley rats received daily intraperitoneal injections of dexamethasone or saline for 14 days. On days 1, 3, and 7 after the last dexamethasone treatment (Dexa1, Dexa3, and Dexa7, respectively) or 1 day after saline (control group), the phrenic nerve-hemidiaphragm preparation was dissected for assay. The dose-response curve of rocuronium in Dexa1 was shifted to the right compared to controls, but curves in Dexa3 and Dexa7 were not significantly different. Groups were not significantly different in attaining the train-of-four ratio ≥ 0.9, but the recovery index in Dexa7 was shorter than that in control and Dexa1. Recovery profiles (period of sugammadex reversal) were not correlated with resistance properties but rather with total administered drugs (binding capacity of NMBAs and sugammadex). Protracted dexamethasone exposure induced resistance to rocuronium but seemed to have no effect on sugammadex reversal in the rat diaphragm.
机译:研究报告说,长时间的地塞米松治疗会引起对非去极化神经肌肉阻滞剂(NMBA)的抵抗,并与大鼠the肌的烟碱乙酰胆碱受体相关。在这里,我们研究了长期地塞米松给药对罗库溴铵的敏感性和当被舒美葡糖逆转时对罗库溴铵敏感性和恢复曲线的影响。此外,我们观察了停药后药效学变化的恢复期。 Sprague-Dawley大鼠每天腹膜内注射地塞米松或生理盐水14天。在最后一次地塞米松治疗后的第1、3和7天(分别是Dexa1,Dexa3和Dexa7)或盐水(对照组)后第1天,解剖the神经半nerve制备物进行分析。与对照相比,Droxa1中罗库溴铵的剂量反应曲线向右移动,但Dexa3和Dexa7中的曲线没有显着差异。各组在达到四轮传动比≥0.9方面无显着差异,但Dexa7的恢复指数短于对照组和Dexa1。恢复曲线(舒马葡糖逆转的时期)与耐药性无关,而与总给药药物(NMBA和舒马葡糖的结合能力)相关。长时间的地塞米松暴露诱导对罗库溴铵具有抗药性,但似乎对大鼠隔膜中的舒马葡糖逆转没有影响。

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