首页> 外文期刊>Pharmacology and Toxicology: An International Journal >Aspects on tail-flick, hot-plate and electrical stimulation tests for morphine antinociception.
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Aspects on tail-flick, hot-plate and electrical stimulation tests for morphine antinociception.

机译:关于吗啡抗伤害感受的甩尾,热板和电刺激试验方面。

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The objective of this study was to compare the results of three nociceptive tests, tail-flick, hot-plate and electrical stimulation vocalisation, reflecting the responses from different sites in the CNS. A subcutaneous morphine dose (5 mg/kg) was administered to three parallel groups of rats in which the nociceptive response was measured by one of the three methods. The baseline decreased during the period of measurement for the hot-plate test, but remained stable for the other methods. The spinally mediated tail-flick response was more sensitive to the morphine effects as compared to the supraspinally mediated hot-plate and electrical stimulation vocalisation responses. The electrical stimulation vocalisation-test demonstrated more even effect-time profiles and less variability among the rats than did the tail-flick and the hot-plate methods. In the tail-flick group, 59% of the observations attained the cut-off latency at this morphine dose, leading to underestimation of the peak effect, the area under the effect curve (AUEC), and the variability among the rats. In the hot-plate group, 13% of the observations were at the cut-off latency, and 2% in the electrical stimulation vocalisation group. Different ways of presenting the data are discussed. In conclusion, the test selected for measuring the nociceptive response will influence the effect-time profile and subsequently any pharmacodynamic parameters describing it.
机译:这项研究的目的是比较三种伤害性测试的结果,甩尾,热板和电刺激发声,以反映中枢神经系统不同部位的反应。将皮下吗啡剂量(5 mg / kg)施用于三个平行组的大鼠,其中通过三种方法之一测量伤害感受性。在热板测试的测量期间,基线下降,但对于其他方法,基线保持稳定。与脊髓上介导的热板和电刺激发声反应相比,脊髓介导的甩尾反应对吗啡效应更为敏感。与甩尾法和热板法相比,电刺激发声测试表明大鼠的效果时间曲线更均匀,变异性更小。在甩尾组中,有59%的观察值在该吗啡剂量下达到了截止潜伏期,导致低估了峰值效应,效应曲线下面积(AUEC)和大鼠之间的变异性。在热板组中,有13%的观察是在截止潜伏期,在电刺激发声组中有2%。讨论了呈现数据的不同方式。总之,为测量伤害性反应而选择的测试将影响作用时间曲线,进而影响描述它的任何药效学参数。

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