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布比卡因、克林霉素和庆大霉素在临床浓度下是否增强罗库溴铵诱导的神经肌肉阻滞?

Do bupivacaine, clindamycin, and gentamicin at their clinical concentrations enhance rocuronium-induced neuromuscular block?

机构信息

Department of Anesthesiology and Pain Medicine, Dong-A University Medical College, Busan, Korea.

出版信息

Korean J Anesthesiol. 2013 Apr;64(4):346-52. doi: 10.4097/kjae.2013.64.4.346. Epub 2013 Apr 22.

Abstract

BACKGROUND

Bupivacaine, clindamycin, and gentamicin inhibit neuromuscular (NM) conduction. When they are combined, they may synergistically reduce the effective concentration of each to the therapeutic concentration in augmenting rocuronium-induced NM block. Thus, the aim of this study was to investigate whether combinations of the three drugs, at around their therapeutic concentrations, potentiate rocuronium-induced NM block.

METHODS

Fifty-seven left-phrenic nerve hemidiaphragms (Male S-D rats, 150-250 g) were hung in a 20-ml organ bath filled with Krebs solution. Three consecutive single-twitch tensions (0.1 Hz) and one tetanic tension (50 Hz for 1.9 s) were obtained. A Krebs solution was premixed with concentration sets of bupivacaine and clindamycin, bupivacaine and gentamicin, or bupivacaine, clindamycin and gentamicin. Then, the concentration of rocuronium was cumulatively increased in the Krebs solution (1, 3, 5, 7, 9, 12, 14, 16, 18, and 20 µM) until an 80% to 90% reduction in single twitch was attained. The effective concentrations for each experiment were determined with the probit model.

RESULTS

The combinations of bupivacaine, clindamycin, and gentamicin enhanced rocuronium-induced NM block. When the three drugs were applied simultaneously, their concentrations were reduced to near-therapeutic levels in potentiating the action of rocuronium.

CONCLUSIONS

Bupivacaine, clindamycin, and gentamicin blocked NM conduction, and when all three drugs were applied together, they augmented rocuronium-induced NM block at their near-therapeutic concentrations. Clinicians should be aware of the cooperability in NM block between drugs that interrupt NM conduction.

摘要

背景

布比卡因、克林霉素和庆大霉素抑制神经肌肉(NM)传导。当它们联合使用时,可能会协同作用,将每种药物的有效浓度降低到增强罗库溴铵诱导的 NM 阻滞的治疗浓度。因此,本研究旨在探讨三种药物在接近治疗浓度时的组合是否增强罗库溴铵诱导的 NM 阻滞。

方法

将 57 个左膈神经半膈肌(雄性 S-D 大鼠,150-250g)悬挂在充满 Krebs 溶液的 20-ml 器官浴中。获得三个连续的单次抽搐张力(0.1Hz)和一个强直张力(50Hz 持续 1.9s)。Krebs 溶液与布比卡因和克林霉素、布比卡因和庆大霉素或布比卡因、克林霉素和庆大霉素的浓度组合预先混合。然后,在 Krebs 溶液中累积增加罗库溴铵的浓度(1、3、5、7、9、12、14、16、18 和 20µM),直到单颤搐减少 80%至 90%。用概率单位模型确定每个实验的有效浓度。

结果

布比卡因、克林霉素和庆大霉素的组合增强了罗库溴铵诱导的 NM 阻滞。当三种药物同时应用时,它们的浓度在增强罗库溴铵的作用时降低到接近治疗水平。

结论

布比卡因、克林霉素和庆大霉素阻断 NM 传导,当三种药物同时应用时,它们在接近治疗浓度时增强罗库溴铵诱导的 NM 阻滞。临床医生应注意 NM 阻断药物之间 NM 传导的协同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3085/3640168/66fc284478bf/kjae-64-346-g001.jpg

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