Mogil J S, Kest B, Sadowski B, Belknap J K
Research Service, Veterans Administration Medical Center, Portland, Oregon, USA.
J Pharmacol Exp Ther. 1996 Feb;276(2):532-44.
Several genetic mouse models of opiate sensitivity have been identified or produced in an attempt to investigate mechanisms underlying individual variation in responses to opiate drugs like morphine. The major models in use presently are the DBA/2 (DBA) versus C57BL/6 (C57) inbred strains, the recombinantly inbred CXBK strain, and mouse lines selectively bred for high- and low-magnitude antinociception after swim stress (HA and LA lines, respectively) or levorphanol administration (HAR and LAR lines, respectively). The hot-plate test, an assay of acute, thermal nociception, was used in the selection of the HA/LA and HAR/LAR lines, and has largely been used to characterize the differential opiate sensitivity of the DBA (high) and C57 (low) strains and the deficient sensitivity of the CXBK strain. There exist, however, many other nociceptive assays used with murine subjects; the most common are the tail-flick/withdrawal test, the acetic acid abdominal constriction test and the formalin test. In the present experiment, baseline nociceptive sensitivities and morphine antinociceptive dose-response relationships (0.1-10 mg/kg i.p. or s.c.) were investigated in mice of all four genetic models and in all four major nociceptive assays, with identical parameters. Results indicate a high degree of dissociation between different genetic models, which suggests that these strains differ in their nociceptive and antinociceptive sensitivities due to the effects of very different genetic and physiological mechanisms. In addition, the present findings suggest that morphine inhibits different modalities of nociception via separate mechanisms that can be genetically dissociated and independently altered. Strikingly, in HA/LA and HAR/LAR mice, we find that an inverse relationship exists with respect to morphine antinociceptive sensitivity in the hot-plate and acetic acid abdominal constriction tests, respectively.
为了探究个体对吗啡等阿片类药物反应差异背后的机制,人们已经鉴定或培育了几种对阿片类药物敏感的基因小鼠模型。目前使用的主要模型是近交系DBA/2(DBA)和C57BL/6(C57),重组近交CXBK品系,以及分别在游泳应激(分别为HA和LA品系)或给予左啡诺后(分别为HAR和LAR品系)因高、低强度抗伤害感受而选择性培育的小鼠品系。热板试验是一种急性热伤害感受测定法,用于选择HA/LA和HAR/LAR品系,并且在很大程度上用于表征DBA(高)和C57(低)品系对阿片类药物的不同敏感性以及CXBK品系的敏感性缺陷。然而,还有许多其他用于小鼠实验对象的伤害感受测定法;最常见的是甩尾/缩足试验、醋酸扭体试验和福尔马林试验。在本实验中,在所有四种基因模型的小鼠中以及在所有四种主要伤害感受测定法中,以相同参数研究了基线伤害感受敏感性和吗啡抗伤害感受剂量反应关系(腹腔注射或皮下注射0.1 - 10 mg/kg)。结果表明不同基因模型之间存在高度解离,这表明这些品系由于非常不同的遗传和生理机制的影响,在伤害感受和抗伤害感受敏感性方面存在差异。此外,目前的研究结果表明,吗啡通过可遗传解离和独立改变的不同机制抑制不同类型的伤害感受。令人惊讶的是,在HA/LA和HAR/LAR小鼠中,我们分别发现在热板试验和醋酸扭体试验中,吗啡抗伤害感受敏感性存在反比关系。