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安乃近(双氯芬酸钠)对大鼠单个运动单位的镇痛作用。

Antinociceptive effects of metamizol (dipyrone) in rat single motor units.

作者信息

Mazario J, Herrero J F

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad de Alcalá, Madrid, Spain.

出版信息

Neurosci Lett. 1999 Oct 29;274(3):179-82. doi: 10.1016/s0304-3940(99)00721-1.

DOI:10.1016/s0304-3940(99)00721-1
PMID:10548419
Abstract

Metamizol has been considered as a peripherally acting non-steroidal antiinflammatory drug, though a central action is possible. The aim of the present study was to elucidate if metamizol induces antinociception in the single motor unit preparation, in normal rats versus rats with carrageenan-induced monoarthritis, and whether this action is produced at central and/or peripheral sites. Metamizol induced a potent antinociceptive effect in both groups of animals, though the effect on responses evoked by natural stimulation was stronger in hyperalgesic rats. Metamizol also depressed wind-up in a dose-dependent manner. We conclude that metamizol is a potent antinociceptive agent both in normal and hyperalgesic animals and that the effect was induced both at peripheral and central sites, at the level of the spinal cord.

摘要

安乃近一直被视为一种外周作用的非甾体抗炎药,不过也可能存在中枢作用。本研究的目的是阐明安乃近在单运动单位制备中是否能诱导正常大鼠和角叉菜胶诱导的单关节炎大鼠产生抗伤害感受,以及这种作用是在中枢和/或外周部位产生的。安乃近在两组动物中均诱导出强效的抗伤害感受作用,不过对超敏大鼠自然刺激诱发反应的作用更强。安乃近还以剂量依赖性方式抑制了累积放电。我们得出结论,安乃近在正常和超敏动物中都是一种强效的抗伤害感受剂,且这种作用是在脊髓水平的外周和中枢部位诱导产生的。

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Antinociceptive effects of metamizol (dipyrone) in rat single motor units.安乃近(双氯芬酸钠)对大鼠单个运动单位的镇痛作用。
Neurosci Lett. 1999 Oct 29;274(3):179-82. doi: 10.1016/s0304-3940(99)00721-1.
2
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A nonopioid analgesic acts upon the PAG-RVM axis to reverse inflammatory hyperalgesia.非阿片类镇痛药作用于中脑导水管周围灰质-延髓头端腹内侧网状结构轴,以逆转炎症性痛觉过敏。
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引用本文的文献

1
Sensory nerves have altered function contralateral to a monoarthritis and may contribute to the symmetrical spread of inflammation.感觉神经在单关节炎对侧的功能发生改变,可能促使炎症对称扩散。
Eur J Neurosci. 2007 Aug;26(4):935-42. doi: 10.1111/j.1460-9568.2007.05737.x.
2
Comparison of the antinociceptive activity of two new NO-releasing derivatives of the NSAID S-ketoprofen in rats.非甾体抗炎药S-酮洛芬的两种新型一氧化氮释放衍生物在大鼠体内的抗伤害感受活性比较。
Br J Pharmacol. 2004 Nov;143(5):533-40. doi: 10.1038/sj.bjp.0705958. Epub 2004 Sep 27.
3
NCX-701 (nitroparacetamol) is an effective antinociceptive agent in rat withdrawal reflexes and wind-up.
NCX-701(硝酰对乙酰氨基酚)在大鼠戒断反射和痛觉过敏中是一种有效的抗伤害感受剂。
Br J Pharmacol. 2002 Mar;135(6):1556-62. doi: 10.1038/sj.bjp.0704589.