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硬膜外给予载新斯的明纳米纤维可延长大鼠的镇痛时间。

Epidural administration of neostigmine-loaded nanofibers provides extended analgesia in rats.

作者信息

Yosefifard Masoomeh, Hassanpour-Ezatti Majid

机构信息

Department of Biology, Sciences School, Shahed University, Tehran, IRAN.

出版信息

Daru. 2014 Nov 18;22(1):73. doi: 10.1186/s40199-014-0073-6.

Abstract

BACKGROUND

In this study, neostigmine-loaded electrospun nanofibers were prepared and then their efficacy and duration of analgesic action were studied after epidural administration in rats by repeated tail flick and formalin tests.

METHODS

The neostigmine poly vinyl alcohol (PVA) nanofibers were fabricated by electrospinning methods. The nanofibers (1 mg) were injected into the lumbar epidural space (L5-L6) of rats (n = 6). Cerebrospinal fluid samples of rats were collected 1, 5 and 24 hours after injection and then were sampled once weekly for 4 weeks. Free-neostigmine concentration was measured in the samples spectrophotometrically. Rat nociceptive responses were evaluated by repeated tail-flick and formalin tests for 5 weeks after the nanofibers (1 mg) injection. Locomotor activity of rats was measured in the open-field at the same period.

RESULTS

The cerebrospinal fluid concentration of free neostigmine reached 5 μg/ml five hours after injection and remained constant until the end of the experiments. The tail-flick latency of treated rats was significantly (p < 0.01) increased and remained constant up to 4 weeks. Pain scores of the rats in both phases of formalin test were significantly (p < 0.01) reduced during the same periods, Epidural injection of the nanofibers had no effect on locomotor activity of rats in an open-field.

CONCLUSIONS

Our results indicate that the neostigmine nanofibers can provide sustained release of neostigmine for induction of prolonged analgesia after epidural administration. High tissue distribution and penetration of the nanofibers in dorsal horn can increase thermal and chemical analgesia duration without altering locomotor activity in rats for 4 weeks.

摘要

背景

在本研究中,制备了负载新斯的明的电纺纳米纤维,然后通过重复甩尾试验和福尔马林试验研究了其在大鼠硬膜外给药后的镇痛效果和作用持续时间。

方法

采用电纺法制备新斯的明聚乙烯醇(PVA)纳米纤维。将纳米纤维(1毫克)注入大鼠(n = 6)的腰段硬膜外腔(L5-L6)。在注射后1、5和24小时收集大鼠的脑脊液样本,然后每周取样一次,共4周。用分光光度法测定样本中的游离新斯的明浓度。在注射纳米纤维(1毫克)后5周内,通过重复甩尾试验和福尔马林试验评估大鼠的伤害性反应。同期在旷场中测量大鼠的运动活性。

结果

注射后5小时,脑脊液中游离新斯的明浓度达到5微克/毫升,并在实验结束前保持恒定。治疗组大鼠的甩尾潜伏期显著延长(p < 0.01),并在4周内保持恒定。在同一时期,福尔马林试验两个阶段的大鼠疼痛评分均显著降低(p < 0.01)。硬膜外注射纳米纤维对大鼠在旷场中的运动活性没有影响。

结论

我们的结果表明,新斯的明纳米纤维在硬膜外给药后可实现新斯的明的持续释放,从而诱导长时间的镇痛。纳米纤维在背角的高组织分布和穿透性可延长热镇痛和化学镇痛的持续时间,且在4周内不改变大鼠的运动活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40e4/4243326/952445147550/40199_2014_73_Fig1_HTML.jpg

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