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全身应用普鲁卡因、利多卡因和丁卡因对小鼠痛觉的影响。

The effects of systemic procaine, lidocaine and dimethocaine on nociception in mice.

作者信息

Rigon A R, Takahashi R N

机构信息

Departamento de Farmacologia, Universidade Federal de Santa Catarina, Florianópolis, Brasil.

出版信息

Gen Pharmacol. 1996 Jun;27(4):647-50. doi: 10.1016/0306-3623(95)02079-9.

DOI:10.1016/0306-3623(95)02079-9
PMID:8853299
Abstract
  1. Different local anesthetics were tested for analgesic activity in three antinociceptive models, the acetic acid-induced abdominal constriction, tail-flick and hot plate tests in the mouse. 2. In the abdominal constriction test, subcutaneous, SC, injection of lidocaine (10, 20 or 30 mg/kg) and dimethocaine (5, 10 or 20 mg/kg) induced dose-dependent antinociceptive responses. Procaine (20, 30 or 50 mg/kg) was also able to reduce the response to noxious chemical stimuli. 3. The IP injection of lidocaine and dimethocaine significantly inhibited the tail-flick and paw-licking hot plate responses; procaine was weak or inactive in these tests, in which heat was the noxious stimulus. 4. Taken together, these results suggest that antinociception produced by systemically administered lidocaine and dimethocaine at nontoxic doses in mice is due, at least in part, to their central effects.
摘要
  1. 在三种抗伤害感受模型(醋酸诱导的小鼠腹部收缩、甩尾和热板试验)中测试了不同局部麻醉药的镇痛活性。2. 在腹部收缩试验中,皮下注射利多卡因(10、20或30毫克/千克)和地美卡因(5、10或20毫克/千克)可诱导剂量依赖性抗伤害感受反应。普鲁卡因(20、30或50毫克/千克)也能够降低对有害化学刺激的反应。3. 腹腔注射利多卡因和地美卡因可显著抑制甩尾和舔爪热板反应;在这些以热作为有害刺激的试验中,普鲁卡因作用较弱或无活性。4. 综合来看,这些结果表明,小鼠全身给予无毒剂量的利多卡因和地美卡因所产生的抗伤害感受至少部分归因于它们的中枢作用。

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