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全身性妥卡尼、利多卡因和布比卡因对大鼠痛觉感受的影响。

The effect of systemic tocainide, lidocaine and bupivacaine on nociception in the rat.

作者信息

Wiesenfeld-Hallin Zsuzsanna, Lindblom Ulf

机构信息

Department of Clinical Neurophysiology, Huddinge University Hospital, S-141 86 Huddinge, and Department of Neurology, Karolinska Hospital, S-104 01 StockholmSweden.

出版信息

Pain. 1985 Dec;23(4):357-360. doi: 10.1016/0304-3959(85)90005-3.

DOI:10.1016/0304-3959(85)90005-3
PMID:3937115
Abstract

The analgesic properties of systemically administered tocainide, a primary amine congener of lidocaine with a longer duration of action, were examined in rats. Significant antinociception, as assayed on the hot-plate test, was observed after i.p. tocainide at doses below toxic levels. No antinociception was seen with non-toxic doses of lidocaine or bupivacaine.

摘要

在大鼠中研究了全身给药的妥卡尼(利多卡因的一种伯胺同系物,作用持续时间更长)的镇痛特性。腹腔注射低于中毒剂量的妥卡尼后,在热板试验中观察到显著的抗伤害感受作用。无毒剂量的利多卡因或布比卡因未观察到抗伤害感受作用。

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The management of central post-stroke pain.中风后中枢性疼痛的管理。
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Antinociception induced by systemic administration of local anaesthetics depends on a central cholinergic mechanism.全身给予局部麻醉药所诱导的镇痛作用取决于中枢胆碱能机制。
Br J Pharmacol. 1987 Dec;92(4):711-21. doi: 10.1111/j.1476-5381.1987.tb11375.x.
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Systemic tocainide relieves mechanical hypersensitivity and normalizes the responses of hyperexcitable dorsal horn wide-dynamic-range neurons after transient spinal cord ischemia in rats.全身性妥卡尼可缓解大鼠短暂性脊髓缺血后机械性超敏反应,并使过度兴奋的背角广动力范围神经元的反应恢复正常。
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