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首页> 外文期刊>Acta anaesthesiologica Taiwanica : >Antinociceptive effects of combination of Tramadol and Acetaminophen on painful diabetic neuropathy in streptozotocin-induced diabetic rats
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Antinociceptive effects of combination of Tramadol and Acetaminophen on painful diabetic neuropathy in streptozotocin-induced diabetic rats

机译:曲马多和对乙酰氨基酚联合使用对链脲佐菌素诱导的糖尿病大鼠糖尿病神经病变的镇痛作用

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Objective: The purpose of this study was to establish the streptozotocin (STZ)-induced diabetic model with rats and investigate the antinociceptive effect of combination of Tramadol (TR) and Acetaminophen (NAPA) on the animal model for the first time. Methods: Diabetic model was induced by a single injection of STZ (60 mg/kg, intraperitoneal). Nociceptive thresholds were measured by means of electronic von Frey test, hot-plate test, and tail-flick test. On the 28th day of diabetes induction, diabetic rats with significant hyperalgesia were randomly divided into three groups: TR, NAPA, and TR-NAPA combination group. Each group was randomly divided into four subgroups. Three geometric series of drugs were given to each group respectively. Antinociceptive effects of the drugs were assessed at 15, 30, 60, 120, and 180 minutes after drug administration. 50% Maximum antinociceptive effect of each drug was determined by probit analysis, whereas interaction between TR and NAPA was evaluated by isobolographic analysis. Results: Hyperalgesia, along with hyperglycemia, developed 4 days after STZ injection and persisted at all tested time points until 28 days. TR, NAPA, and TR-NAPA combination administration all produced dose-dependent antinociceptive effects. Isobolographic analysis showed a significant deviation of TR/NAPA 50% maximum antinociceptive effect (in tail-flick test, but not in von Frey test) from the additive line. Conclusions: Combination of the two drugs produces an additive antinociceptive effect in tail-flick test, whereas probable additive antinociceptive effect in von Frey test in painful diabetic neuropathy rats.
机译:目的:本研究的目的是建立大鼠链脲佐菌素(STZ)诱导的糖尿病模型,并首次研究曲马多(TR)和对乙酰氨基酚(NAPA)联合使用对动物模型的抗伤害作用。方法:单次注射STZ(60 mg / kg,腹膜内)诱导出糖尿病模型。伤害阈值通过电子冯·弗雷(von Frey)测试,热板测试和甩尾测试进行测量。诱导糖尿病的第28天,将具有明显痛觉过敏的糖尿病大鼠随机分为三组:TR,NAPA和TR-NAPA联合治疗组。每组随机分为四个亚组。每组分别给予三个几何系列的药物。在给药后第15、30、60、120和180分钟评估药物的抗伤害感受作用。通过概率分析确定每种药物的最大50%止痛效果,而TR和NAPA之间的相互作用通过等效线描记法分析进行评估。结果:痛觉过敏和高血糖症发生在STZ注射后4天,并在所有测试时间点持续到28天。 TR,NAPA和TR-NAPA联合给药均可产生剂量依赖性抗伤害感受作用。等效线描记法分析显示,TR / NAPA最大抗伤害作用50%(在甩尾试验中,在von Frey试验中没有)明显偏离添加剂系。结论:两种药物的组合在甩尾试验中产生加性抗伤害感受作用,而在von Frey试验中可能对糖尿病性神经病大鼠产生加成抗伤害感受作用。

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