Grant S J, Redmond D E
Pharmacol Biochem Behav. 1982 Oct;17(4):655-8. doi: 10.1016/0091-3057(82)90340-9.
The effects of the alpha-2 adrenergic agonist, clonidine, on the "quasi-morphine withdrawal syndrome" (QMWS) were examined in drug naive rats. The QMWS was induced by combined systemic administration of iso-butyl-methylxanthine (IBMX: 15 mg/kg, IP) and naloxone (1 mg/kg, IP). Pretreatment with clonidine (50 micrograms/kg, IP) significantly decreased the incidence of 11 out of 16 withdrawal signs. Since clonidine suppresses signs and symptoms of true morphine withdrawal, the suppression of methylxanthine effects demonstrates an additional similarity of the QMWS to true morphine withdrawal. These results suggest that a significant common neural mechanism of both the QMWS and true morphine withdrawal is affected by clonidine.
在未接触过药物的大鼠中,研究了α-2肾上腺素能激动剂可乐定对“准吗啡戒断综合征”(QMWS)的影响。通过联合腹腔注射异丁基甲基黄嘌呤(IBMX:15mg/kg)和纳洛酮(1mg/kg)诱导产生QMWS。可乐定(50μg/kg,腹腔注射)预处理显著降低了16种戒断症状中11种症状的发生率。由于可乐定可抑制真正吗啡戒断的体征和症状,因此它对甲基黄嘌呤效应的抑制表明QMWS与真正吗啡戒断存在额外的相似性。这些结果表明,可乐定影响了QMWS和真正吗啡戒断的一个重要共同神经机制。