Yamazaki A, Kaneto H
Jpn J Pharmacol. 1985 Dec;39(4):461-5. doi: 10.1254/jjp.39.461.
A single dose of clonidine developed tolerance to its analgesic effect. The tolerance reached its peak acutely on the 2nd day and lasted more than 5 days. Neither the analgesic effect nor the development of tolerance was modified by the pretreatment with naloxone. On the 2nd day, clonidine tolerant animals were also tolerant to morphine, but morphine tolerant animals, after a single dose of morphine on the 1st day, were not tolerant to clonidine. On the 5th day, however, clonidine tolerant animals were tolerant to morphine, and vice versa. Thus, the interaction between morphine and clonidine was "one-way" on the 2nd day, and cross-tolerance was only demonstrated on the 5th day. With a treatment with clonidine plus naloxone on the 1st day, the development of cross-tolerance to morphine was completely suppressed on the 2nd day but not on the 5th day. These results confirmed our previous finding that acute and delayed tolerance are different in nature, and the development of tolerance to morphine and clonidine are partially underlaid with a common mechanism which is not mediated by opioid receptors.
单次剂量的可乐定对其镇痛作用产生了耐受性。耐受性在第2天急性达到峰值,并持续超过5天。纳洛酮预处理既不改变镇痛效果,也不改变耐受性的发展。在第2天,可乐定耐受的动物对吗啡也有耐受性,但吗啡耐受的动物在第1天单次注射吗啡后,对可乐定没有耐受性。然而,在第5天,可乐定耐受的动物对吗啡有耐受性,反之亦然。因此,吗啡和可乐定之间的相互作用在第2天是“单向的”,交叉耐受性仅在第5天表现出来。在第1天用可乐定加纳洛酮治疗,对吗啡的交叉耐受性发展在第2天被完全抑制,但在第5天没有被抑制。这些结果证实了我们之前的发现,即急性耐受性和延迟耐受性在本质上是不同的,对吗啡和可乐定耐受性的发展部分基于一种不通过阿片受体介导的共同机制。