Adams M L, Sewing B N, Chen J, Meyer E R, Cicero T J
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Alcohol Clin Exp Res. 1995 Feb;19(1):195-9. doi: 10.1111/j.1530-0277.1995.tb01492.x.
Evidence has been reported supporting the hypothesis that nitric oxide (NO) partially mediates the expression of morphine dependence. To examine whether NO-related agents also affect the expression of alcohol dependence, adult male rats were treated chronically with alcohol. Upon withdrawal of alcohol administration, abstinence signs were observed after treatment with a NO synthase (NOS) inhibitor, NG-nitro-L-arginine methyl ester (NAME), or a NO donor, isosorbide dinitrate (ISDN). Withdrawal severity was based primarily on the presence and intensity of tremors, rigidity, hyperactivity, and spontaneous and audiogenic convulsions. The NOS inhibitor, NAME (10-100 mg/kg), injected during alcohol withdrawal significantly inhibited withdrawal severity decreasing the intensity of signs of hyperactivity, tremors, and rigidity, but not affecting the occurrence of convulsions. The NO donor, ISDN (30 mg/kg), administered during alcohol withdrawal significantly increased the severity of most withdrawal signs. These results suggest that NO mediates some aspects of the expression of alcohol dependence.
有证据表明支持这样的假说,即一氧化氮(NO)部分介导吗啡依赖性的表达。为了研究与NO相关的药物是否也会影响酒精依赖性的表达,成年雄性大鼠长期接受酒精处理。在停止给予酒精后,用一氧化氮合酶(NOS)抑制剂NG-硝基-L-精氨酸甲酯(NAME)或一氧化氮供体硝酸异山梨酯(ISDN)处理后观察到戒断症状。戒断严重程度主要基于震颤、僵硬、多动以及自发和听源性惊厥的存在和强度。在酒精戒断期间注射的NOS抑制剂NAME(10 - 100毫克/千克)显著抑制戒断严重程度,降低多动、震颤和僵硬症状的强度,但不影响惊厥的发生。在酒精戒断期间给予的一氧化氮供体ISDN(30毫克/千克)显著增加了大多数戒断症状的严重程度。这些结果表明NO介导了酒精依赖性表达的某些方面。