Luján M, Rodríguez R
Br J Pharmacol. 1981 Aug;73(4):859-66. doi: 10.1111/j.1476-5381.1981.tb08739.x.
1 Physical dependence was produced in ilea from naive guinea-pigs by exposure of the tissue to different opiates for logarithmically-spaced periods of time (20-320 min). The responsiveness of the tissue to naloxone, as indicated by a strong contracture of the ileum, was enhanced in contrast to that found in intestines not exposed to opiates. 2 The dose-response curves to naloxone obtained in tissues individually exposed to different opiates showed that their relative potency in increasing sensitivity to naloxone was as follows: levorphan greater than morphine greater than Met-enkephalin greater than nalorphine greater than pentazocine. 3 The naloxone-induced response was dose-dependent and was directly related to the opiate concentration and length of exposure. 4 Dextrorphan the inactive isomer of levorphan, did not increase the responsiveness of the tissues to the narcotic antagonist, indicating that the phenomenon is stereospecific. 5 The naloxone-induced contraction in ilea exposed for 320 min to morphine (1 x 10(-6)M) was not prevented or suppressed by the administration of a large dose of morphine (1 x 10(-5)M) before or immediately after the naloxone challenge. 6 The evidence presented here shows that a phenomenon resembling in vivo opiate physical dependence can be acutely produced in vitro with pharmacological characteristics similar to other naloxone-induced abstinence effects.
通过将来自未经接触的豚鼠的回肠组织暴露于不同阿片类药物中对数间隔的时间段(20 - 320分钟),产生了身体依赖性。与未接触阿片类药物的肠道相比,回肠强烈收缩所表明的组织对纳洛酮的反应性增强。
在分别暴露于不同阿片类药物的组织中获得的对纳洛酮的剂量 - 反应曲线表明,它们在增加对纳洛酮敏感性方面的相对效力如下:左啡诺大于吗啡大于甲硫氨酸脑啡肽大于烯丙吗啡大于喷他佐辛。
纳洛酮诱导的反应呈剂量依赖性,且与阿片类药物浓度和暴露时间直接相关。
左啡诺的无活性异构体右啡烷并未增加组织对麻醉拮抗剂的反应性,表明该现象具有立体特异性。
在纳洛酮激发前或激发后立即给予大剂量吗啡(1×10⁻⁵M),并未阻止或抑制暴露于吗啡(1×10⁻⁶M)320分钟的回肠中纳洛酮诱导的收缩。
此处提供的证据表明,类似于体内阿片类药物身体依赖性的现象可在体外急性产生,其药理学特征与其他纳洛酮诱导的戒断效应相似。