已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Dose-dependent neurotoxicity caused by the addition of perineural dexmedetomidine to ropivacaine for continuous femoral nerve block in rabbits

罗哌卡因 医学 右美托咪定 股神经 麻醉 生理盐水 神经阻滞 坐骨神经 神经毒性 解剖 毒性 内科学 镇静
作者
Haili Wang,Guangying Zhang,Wei-xin Dai,Lipei Shu,Qiu-Feng Wei,Ruo-Fang Zheng,Cheng-Li Lin
出处
期刊:Journal of International Medical Research [SAGE Publishing]
卷期号:47 (6): 2562-2570 被引量:7
标识
DOI:10.1177/0300060519847368
摘要

Objective This study was designed to evaluate the neurotoxicity of dexmedetomidine combined with ropivacaine for continuous femoral nerve block in rabbits. Methods Thirty New Zealand rabbits were randomly divided into 5 groups of 6 rabbits each and received a continuous femoral nerve block with saline; 0.25% ropivacaine; or 1, 2, or 3 µg/mL of dexmedetomidine added to 0.25% ropivacaine (Groups A–E, respectively). Sensory and motor function was assessed after the nerve block. The rabbits were anesthetized and killed after 48 hours of a continuous femoral nerve block, and the femoral nerves were removed for light and electron microscopy analyses. Results The behavior scores were highest in Group A at 2 and 6 hours after injection. The scores were higher in Groups B and C than in Groups D and E at these same time points. All groups showed normal pathological tissues in the femoral nerves under optical microscopy. Under electron microscopy, histological abnormalities were observed only in Group E; none of the other groups exhibited pathological abnormalities. Quantitative analysis of the myelin sheath area revealed no significant difference in the axonal area, total area of the myelin sheath, or ratio of the total axonal area to the total area of the myelin sheath in all groups. Conclusion The lowest doses of dexmedetomidine (1 and 2 µg/mL) combined with 0.25% ropivacaine for continuous femoral nerve block resulted in no neurotoxic lesions, but the higher dose (3 µg/mL) resulted in neurotoxic lesions in this rabbit experimental model.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1234567xjy完成签到,获得积分10
刚刚
MAMAMIYA发布了新的文献求助10
刚刚
关山完成签到,获得积分20
刚刚
乐乐应助znlm采纳,获得10
1秒前
2秒前
哈哈王子发布了新的文献求助10
3秒前
天天快乐应助2415060217采纳,获得10
3秒前
史萌发布了新的文献求助10
4秒前
桐桐应助坚果燕麦采纳,获得10
4秒前
duo完成签到,获得积分10
5秒前
6秒前
jksxxmxt123完成签到,获得积分10
6秒前
Joehq_1203应助石头采纳,获得10
6秒前
矮冬瓜完成签到 ,获得积分10
8秒前
科研通AI6.2应助Makula采纳,获得10
9秒前
CAOHOU应助科研通管家采纳,获得10
9秒前
关山发布了新的文献求助10
9秒前
所所应助科研通管家采纳,获得10
9秒前
桐桐应助科研通管家采纳,获得20
9秒前
clara完成签到 ,获得积分10
9秒前
共享精神应助科研通管家采纳,获得10
9秒前
JamesPei应助科研通管家采纳,获得10
10秒前
852应助科研通管家采纳,获得10
10秒前
Hello应助科研通管家采纳,获得10
10秒前
10秒前
懦弱的问芙完成签到,获得积分10
10秒前
科研通AI6.2应助科研通管家采纳,获得100
10秒前
嘉心糖应助科研通管家采纳,获得30
10秒前
10秒前
英姑应助科研通管家采纳,获得10
10秒前
10秒前
10秒前
充电宝应助科研通管家采纳,获得30
10秒前
CipherSage应助科研通管家采纳,获得10
10秒前
夜雨发布了新的文献求助10
11秒前
一路有你完成签到 ,获得积分0
12秒前
是多多呀完成签到 ,获得积分10
15秒前
Joehq_1203应助南音采纳,获得10
18秒前
风中小懒虫完成签到,获得积分10
18秒前
小天小天完成签到 ,获得积分10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Netter collection Volume 9 Part I upper digestive tract及Part III Liver Biliary Pancreas 3rd 2024 的超高清PDF,大小约几百兆,不是几十兆版本的 1050
Current concept for improving treatment of prostate cancer based on combination of LH-RH agonists with other agents 1000
Research Handbook on the Law of the Sea 1000
Contemporary Debates in Epistemology (3rd Edition) 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6165056
求助须知:如何正确求助?哪些是违规求助? 7992562
关于积分的说明 16619679
捐赠科研通 5271867
什么是DOI,文献DOI怎么找? 2812621
邀请新用户注册赠送积分活动 1792715
关于科研通互助平台的介绍 1658583