阿司匹林和双吡喃酮对小鼠抗痛感活性的时间药理学评价

E. Yıldırım, F. Kılıç, B. Sirmagul, K. Erol
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引用次数: 0

摘要

大量的生理节律受中枢神经系统控制,其中包括激素的分泌。许多药物的效力和毒性也会随着服用时间的不同而变化。也有一些关于疼痛敏感性的生物节律的研究。在本研究中,我们对阿司匹林和双吡酮这两种常用镇痛药的中枢和外周抗痛感作用进行了小鼠时间药理学评价。采用夹尾、甩尾、热板等方法观察100 mg/kg灌胃给药小鼠的中枢抗痛觉活性,并用醋酸拉伸法观察上午9点或晚上9点给药小鼠的外周抗痛觉活性。两组间中枢伤害性无明显差异。而醋酸试验对疼痛的敏感性在夜间显著高于白天(p < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronopharmacological evaluation of the antinociceptive activities of aspirin and dipyrone in mice
AbstractA large number of physiological rhythms are controlled by the central nervous system, including hormone secretion. The potency and toxicity of many drugs also change according to the time when they are administered. There are also some studies of the biological rhythms in pain sensitivity. In the present study, central and peripheral antinociceptive effects of aspirin and dipyrone, commonly used analgesics, were evaluated chronopharmacologically in mice. The central antinociceptive activities of these drugs administered intraperiotoneally (100 mg/kg) were investigated in mice using tail clip, tail flick and hot plate tests, and the peripheral antinociceptive activities of these drugs were investigated using a stretching test with acetic acid when the drugs were administered at 9.00 a. m. or 9.00 p. m. The central nociception was not different between the two groups, while the sensitivity to pain was significantly greater with the acetic acid test (p < 0.05) at night than in the daylight in the con...
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