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右美托咪定增强利多卡因的作用:功率谱和神经传导速度分布研究。

Dexmedetomidine augments the effect of lidocaine: power spectrum and nerve conduction velocity distribution study.

作者信息

Dalkilic Nizamettin, Tuncer Seckin, Burat Ilksen

机构信息

N.E. University, Meram School of Medicine, Biophysics Department, Konya, Turkey.

出版信息

BMC Anesthesiol. 2015 Mar 6;15:24. doi: 10.1186/s12871-015-0009-9. eCollection 2015.

Abstract

BACKGROUND

In this study, the individual and combined inhibitory effects of dexmedetomidine and lidocaine on the conduction group of isolated nerve were investigated by determining conduction velocity distribution (CVD) and power spectrum.

METHODS

Electrophysiological compound action potential (CAP) recordings were conducted on isolated rat sciatic nerve before (Con) and 20 minutes after exposure to 1 mM lidocaine (Lido), 21pM dexmedetomidine (Dex) and their combination (Lido + Dex). Then for CVD, mathematical model and for power spectrum Fast Fourier analysis were conducted.

RESULTS

Dexmedetomidine alone made no significant difference in shape and duration of CAPs as compared to Con, on the other hand lidocaine depresses amplitude and prolongs the duration of CAPs, but not more than combination of dexmedetomidine and lidocaine can do. Lidocaine caused a shift in the CVD histogram to relatively slower conducting group significantly while dexmedetomidine did not cause any significant change as compared to Control. Lidocaine, when combined with dexmedetomidine revealed a remarkable effect on the whole CVD histogram by causing almost complete blockage of fast conducting nerve fibers. The relative number of fibers in CVD is conserved for separate applications of anesthetics, but not for their combination. As in CVD, power spectrum shifted from higher to lower frequency region by lidocaine and significantly for lidocaine combined with dexmedetomidine application. Shifts for dexmedetomidine applied group were seen beggarly.

CONCLUSIONS

We have concluded that dexmedetomidine alone did not influence nerve conduction, but when it is used with lidocaine it augments neural conduction blockage effect, especially on fast conducting nerve fibers.

摘要

背景

在本研究中,通过测定传导速度分布(CVD)和功率谱,研究了右美托咪定和利多卡因对离体神经传导组的单独及联合抑制作用。

方法

在离体大鼠坐骨神经上,于暴露于1 mM利多卡因(Lido)、21 pM右美托咪定(Dex)及其组合(Lido + Dex)之前(Con)和之后20分钟进行电生理复合动作电位(CAP)记录。然后对CVD进行数学建模,对功率谱进行快速傅里叶分析。

结果

与Con相比,单独使用右美托咪定对CAP的形状和持续时间无显著差异,另一方面,利多卡因降低了CAP的幅度并延长了其持续时间,但不如右美托咪定和利多卡因联合使用的效果明显。利多卡因使CVD直方图明显向传导较慢的组转移,而与对照组相比,右美托咪定未引起任何显著变化。利多卡因与右美托咪定联合使用时,对整个CVD直方图显示出显著影响,几乎完全阻断了快速传导的神经纤维。在单独应用麻醉剂时,CVD中纤维的相对数量是守恒的,但联合应用时则不然。与CVD情况一样,利多卡因使功率谱从高频区域向低频区域转移,利多卡因与右美托咪定联合应用时这种转移更为显著。右美托咪定应用组的转移则不明显。

结论

我们得出结论,单独使用右美托咪定不影响神经传导,但与利多卡因合用时,它会增强神经传导阻滞作用,尤其是对快速传导的神经纤维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a474/4355462/d64bc88ea6a3/12871_2015_9_Fig1_HTML.jpg

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