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喷布洛尔对利多卡因动力学的影响。

Effect of penbutolol on lidocaine kinetics.

作者信息

Ochs H R, Skanderra D, Abernethy D R, Greenblatt D J

出版信息

Arzneimittelforschung. 1983;33(12):1680-1.

PMID:6686773
Abstract

The effect of penbutolol (Betapressin), a stereospecific beta-adrenergic antagonist, on the pharmacokinetics of a single dose of intravenous lidocaine was evaluated in seven healthy volunteers. Subjects received a single 100-mg lidocaine intravenous dose of lidocaine hydrochloride, once in the control state and a second time during coadministration of penbutolol, 60 mg daily. Lidocaine volume of distribution was significantly increased during penbutolol treatment (4.9 vs 3.4 l/kg, p less than 0.005), resulting in a significant prolongation of elimination half-life (2.5 vs 2.0 h, p less than 0.025). The mechanism of the distributional shift is not established, but may result from a change in the pattern of peripheral blood flow and therefore the profile of tissue uptake of lidocaine. Total metabolic clearance of lidocaine, however, was not significantly altered by penbutolol (23.0 vs 19.4 ml/min/kg). The present study of healthy volunteers suggests that penbutolol increases lidocaine volume of distribution. If the finding also applied to patients, a higher loading dose of lidocaine might be necessary.

摘要

在7名健康志愿者中评估了立体特异性β-肾上腺素能拮抗剂喷布洛尔(倍他新)对单剂量静脉注射利多卡因药代动力学的影响。受试者接受单次100mg盐酸利多卡因静脉注射,一次在对照状态下,第二次在每日合用60mg喷布洛尔期间。在喷布洛尔治疗期间,利多卡因的分布容积显著增加(4.9对3.4L/kg,p<0.005),导致消除半衰期显著延长(2.5对2.0小时,p<0.025)。分布转移的机制尚未明确,但可能是由于外周血流模式的改变以及因此利多卡因组织摄取情况的改变所致。然而,喷布洛尔并未显著改变利多卡因的总代谢清除率(23.0对19.4ml/min/kg)。对健康志愿者的本研究表明,喷布洛尔增加了利多卡因的分布容积。如果该发现也适用于患者,可能需要更高剂量的利多卡因负荷量。

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