St. Paul's Hospital, Vancouver, British Columbia, Canada.
Anesthesiology. 2010 Aug;113(2):438-44. doi: 10.1097/ALN.0b013e3181dfd31b.
We recently found that peripheral administration of the quaternary lidocaine derivative, QX-314, produces long-lasting sensory and motor blockade in animals. The goal of this study was to test whether intrathecal QX-314 has similar properties.
We conducted a randomized, double-controlled, blinded study with female CD-1 mice. Animals in the treatment group received lumbar intrathecal QX-314 (0.5-10 mM; volume, 2 microl; each concentration, n = 6). Normal saline and lidocaine (70 mM) served as negative and positive controls (each group, n = 12), respectively. Animals were tested for up to 3 h for lumbosacral neural blockade and observed for adverse effects.
No animal injected with saline and 11 of 12 (92%) animals injected with lidocaine displayed reversible lumbosacral motor blockade (P < 0.001). QX-314 (5 mM) produced motor blockade in four of the six (67%) and sensory blockade in five of the six animals (83%; P < 0.05 vs. saline). However, six of the six mice (100%) at 5 mM QX-314 and five of the six (83%) at 10 mM exhibited marked irritation; one of the six animals at 5 mM (17%) and two of the six at 10 mM (33%) died. We observed no neural blockade without adverse effects in any animal injected with QX-314. All animals injected with saline and 11 of the 12 (92%) animals injected with lidocaine demonstrated normal behavior.
Lumbar intrathecal QX-314 concentration-dependently produced irritation and death in mice, at lower concentrations than those associated with robust motor blockade. Although QX-314 did produce long-lasting neural blockade, these findings indicate that QX-314 is unlikely to be a suitable candidate for spinal anesthesia in humans.
我们最近发现,外周给予季铵型利多卡因衍生物 QX-314 可在动物中产生持久的感觉和运动阻滞。本研究的目的是测试鞘内 QX-314 是否具有类似的特性。
我们进行了一项随机、双对照、盲法研究,使用雌性 CD-1 小鼠。治疗组动物接受腰段鞘内 QX-314(0.5-10 mM;体积 2 微升;每个浓度,n = 6)。生理盐水和利多卡因(70 mM)分别作为阴性和阳性对照(每组,n = 12)。动物接受测试的时间长达 3 小时,以评估腰骶神经阻滞,并观察不良反应。
注射生理盐水的动物无一例出现可逆性腰骶部运动阻滞,而注射利多卡因的 12 只动物中有 11 只(92%)出现(P < 0.001)。QX-314(5 mM)引起 6 只动物中的 4 只(67%)运动阻滞和 6 只动物中的 5 只(83%)感觉阻滞(P < 0.05 对比生理盐水)。然而,6 只 5 mM QX-314 动物(100%)和 6 只 10 mM QX-314 动物中的 5 只(83%)出现明显刺激;6 只 5 mM 动物中的 1 只(17%)和 6 只 10 mM 动物中的 2 只(33%)死亡。我们未观察到注射 QX-314 后无神经阻滞和不良反应的动物。注射生理盐水的所有动物和注射利多卡因的 12 只动物中的 11 只(92%)表现出正常行为。
鞘内 QX-314 浓度依赖性地在小鼠中引起刺激和死亡,其浓度低于与强烈运动阻滞相关的浓度。尽管 QX-314 确实产生了持久的神经阻滞,但这些发现表明 QX-314 不太可能成为人类脊髓麻醉的合适候选药物。