Malin D H, Lake J R, Payne M C, Short P E, Carter V A, Cunningham J S, Wilson O B
University of Houston-Clear Lake, TX 77058, USA.
Pharmacol Biochem Behav. 1996 Jan;53(1):81-5. doi: 10.1016/0091-3057(95)00202-2.
In a recently introduced rodent model of nicotine abstinence syndrome, the observed signs closely resembled those typical of rat opiate abstinence syndrome. Signs were precipitated by naloxone and potently reversed by morphine as well as nicotine itself, suggesting that nicotine might relieve nicotine abstinence syndrome through releasing endogenous opioids. To test this hypothesis, rats were continuously infused subcutaneously (SC) for 7 days with 9 mg/kg per day nicotine tartrate. Each rat was observed for abstinence signs at 18 and 21 h after termination of infusion. Three minutes before the 21-h test, all rats received 0.35 mg/kg nicotine tartrate, SC; 5 min before the nicotine injection, subjects received 9 or 4.5 mg/kg naloxone or saline alone, SC. Abstinence reversal scores were calculated as signs at 21 h as a percentage of signs at 18 h. Naloxone prevented nicotine alleviation of nicotine abstinence in a dose-related manner. However, naloxone in the absence of a nicotine injection had no effect on abstinence severity in either highly dependent or moderately dependent rats (infused with 9 or 5 mg/kg per day nicotine tartrate, respectively). These results support the hypothesis that endogenous opioids play a role in nicotine dependence and abstinence.
在最近引入的尼古丁戒断综合征啮齿动物模型中,观察到的症状与大鼠阿片类药物戒断综合征的典型症状非常相似。这些症状由纳洛酮引发,并被吗啡以及尼古丁本身有效逆转,这表明尼古丁可能通过释放内源性阿片类物质来缓解尼古丁戒断综合征。为了验证这一假设,给大鼠连续7天皮下注射(SC)每天9毫克/千克的酒石酸尼古丁。在输液结束后的18小时和21小时观察每只大鼠的戒断症状。在21小时测试前3分钟,所有大鼠皮下注射0.35毫克/千克酒石酸尼古丁;在注射尼古丁前5分钟,实验对象分别皮下注射9毫克/千克或4.5毫克/千克纳洛酮或单独注射生理盐水。戒断逆转分数计算为21小时时的症状占18小时时症状的百分比。纳洛酮以剂量相关的方式阻止了尼古丁对尼古丁戒断的缓解作用。然而,在没有注射尼古丁的情况下,纳洛酮对高度依赖或中度依赖大鼠(分别注射每天9毫克/千克或5毫克/千克酒石酸尼古丁)的戒断严重程度没有影响。这些结果支持了内源性阿片类物质在尼古丁依赖和戒断中起作用这一假设。