长期暴露于地塞米松可能不会影响罗库溴铵诱导的神经肌肉阻断的糖马德逆转:一项对大鼠的体内研究。

Ha Yeon Park, Hey Ran Choi, Yong Beom Kim, Seok Kyeong Oh, Taehoon Kim, Hong Seuk Yang, Junyong In
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引用次数: 0

摘要

背景:慢性糖皮质激素暴露与对非去极化神经肌肉阻滞剂的抵抗有关。因此,我们假设暴露于慢性地塞米松的受试者比未暴露于慢性地塞米松的受试者恢复得更快。本研究评估了慢性地塞米松暴露大鼠神经肌肉阻断(NMB)后糖madex诱导的恢复情况。方法:将Sprague-Dawley大鼠分为地塞米松组、对照组和配对喂养组进行体内研究。小鼠每天腹腔注射地塞米松(500 μg/kg)或0.9%生理盐水,连续15 d。为了达到完全的NMB,在第16天给予3.5 mg/kg罗库溴铵。测量恢复时间至四列比值≥0.9,以评估糖madex注射后的完全恢复。结果:各组间给药后恢复时间与四列比值≥0.9的差异无统计学意义(P = 0.531)。罗库溴铵给药后4次训练恢复到第二次抽搐的时间显示,D组NMB持续时间明显短于C组和P组(P = 0.001)。结论:慢性地塞米松暴露并没有缩短糖madex诱导的NMB逆转的恢复时间。然而,本研究结果表明,即使在长期接受类固醇治疗的患者中,也不需要调整糖madex的剂量或给药途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chronic exposure to dexamethasone may not affect sugammadex reversal of rocuronium-induced neuromuscular blockade: an in vivo study on rats.

Chronic exposure to dexamethasone may not affect sugammadex reversal of rocuronium-induced neuromuscular blockade: an in vivo study on rats.

Chronic exposure to dexamethasone may not affect sugammadex reversal of rocuronium-induced neuromuscular blockade: an in vivo study on rats.

Chronic exposure to dexamethasone may not affect sugammadex reversal of rocuronium-induced neuromuscular blockade: an in vivo study on rats.

Background: Chronic glucocorticoid exposure is associated with resistance to nondepolarizing neuromuscular blocking agents. Therefore, we hypothesized that sugammadex-induced recovery would occur more rapidly in subjects exposed to chronic dexamethasone compared to those who were not exposed. This study evaluated the sugammadex-induced recovery profile after neuromuscular blockade (NMB) in rats exposed to chronic dexamethasone.

Methods: Sprague-Dawley rats were allocated to three groups (dexamethasone, control, and pair-fed group) for the in vivo study. The mice received daily intraperitoneal dexamethasone injections (500 μg/kg) or 0.9% saline for 15 days. To achieve complete NMB, 3.5 mg/kg rocuronium was administered on the sixteenth day. The recovery time to a train-of-four ratio ≥ 0.9 was measured to evaluate the complete recovery following the sugammadex injection.

Results: Among the groups, no significant differences were observed in the recovery time to a train-of-four ratio ≥ 0.9 following sugammadex administration (P = 0.531). The time to the second twitch of the train-of-four recovery following rocuronium administration indicated that the duration of NMB was significantly shorter in Group D than that in Groups C and P (P = 0.001).

Conclusions: Chronic exposure to dexamethasone did not shorten the recovery time of sugammadex-induced NMB reversal. However, the findings of this study indicated that no adjustments to sugammadex dosage or route of administration is required, even in patients undergoing long-term steroid treatment.

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