Kolesnikov Yuri, Cristea Marcela, Oksman Galina, Torosjan Armen, Wilson Roger
Department of Anesthesiology and Critical Care, Memorial-Sloan Kettering Cancer Center, 1275 York Ave, New York, NY 10021, USA.
Brain Res. 2004 Dec 17;1029(2):217-23. doi: 10.1016/j.brainres.2004.09.058.
Opioids are effective topical analgesics in the radiant heat tailflick assay and display synergistic interactions with a number of other classes of drugs. To determine whether these actions extend to other types of nociception, we examined the actions of topical morphine and lidocaine in a tail formalin assay in the mouse. Formalin responses in the tail were similar to those seen in the hind paw, but were limited to licking. Unlike the traditional hind paw assay, the time-course of nociceptive behavior in the tail was monophasic; lasting 40-60 min. Morphine, MK-801 and acetylsalicylic acid (ASA) were active systemically in the tail formalin assay with potencies similar to those seen in the second phase of the paw formalin test. Both morphine and lidocaine were active topically in the tail formalin assay, although their time-course of action appeared to be shorter than that of the formalin. However, morphine displayed ceiling effect not seen when it was administered systemically. Lidocaine also had a ceiling effect. When given together, the response to the combination was supra-additive, consistent with our prior studies showing synergy in the radiant heat tailflick assay. These studies validate the formalin assay in the tail and support the topical actions of opioids and other drugs in a second pain model. They also suggest supra-additive interactions between morphine and lidocaine similar to those previously seen. The tail formalin assay will be valuable in assessing the activity of topical drugs.
阿片类药物在辐射热甩尾试验中是有效的局部镇痛药,并与许多其他类药物显示出协同相互作用。为了确定这些作用是否扩展到其他类型的伤害感受,我们在小鼠尾部福尔马林试验中研究了局部应用吗啡和利多卡因的作用。尾部的福尔马林反应与后爪的反应相似,但仅限于舔舐。与传统的后爪试验不同,尾部伤害性反应的时间进程是单相的,持续40 - 60分钟。吗啡、MK - 801和乙酰水杨酸(ASA)在尾部福尔马林试验中全身给药时有活性,其效力与在爪部福尔马林试验的第二阶段所见相似。吗啡和利多卡因在尾部福尔马林试验中局部应用均有活性,尽管它们的作用时间进程似乎比福尔马林的短。然而,吗啡显示出全身给药时未见的封顶效应。利多卡因也有封顶效应。当联合使用时,对组合的反应是超相加的,这与我们之前在辐射热甩尾试验中显示协同作用的研究一致。这些研究验证了尾部福尔马林试验,并支持阿片类药物和其他药物在第二种疼痛模型中的局部作用。它们还表明吗啡和利多卡因之间存在超相加相互作用,类似于之前所见。尾部福尔马林试验在评估局部药物的活性方面将具有价值。