Itzhak Y
Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, Florida 33101, USA.
J Pharmacol Exp Ther. 1997 Aug;282(2):521-7.
Evidence suggests the existence of multiple interactions between dopamine, glutamate and nitric oxide (NO) in brain structures associated with psychomotor stimulation. The present study was undertaken to investigate the effect of the relatively selective inhibitor of the neuronal nitric oxide synthase (NOS) isoform, 7-nitroindazole (7-NI), on the development of sensitization to the locomotor stimulating effect of cocaine and methamphetamine (METH). Male Swiss Webster mice that received 15 mg/kg cocaine once a day for 5 days developed a marked locomotor sensitization to a challenge cocaine (15 mg/kg) or cross-sensitization to a challenge METH (0.5 mg/kg) injection given after a 10-day drug-free period. This treatment also produced a context-dependent sensitization as evident by the sensitized response to a challenge saline injection. Pretreatment with 7-NI (25 mg/kg) 30 min before cocaine administration (5 days) completely blocked the induction of sensitization to cocaine, the cross-sensitization to METH and the conditioned locomotion induced by cocaine. 7-NI when given alone, either acutely or for 5 days, had no significant effect on the locomotor activity of animals. Animals treated with METH (1.0 mg/kg) for 5 days developed marked sensitization to challenge METH (0.5 mg/kg), cross-sensitization to challenge cocaine (15 mg/kg) and context-dependent locomotion. Pretreatment with 7-NI (25 mg/kg) attenuated the sensitized response to METH and the cross-sensitization to cocaine as revealed after a 10-day drug-free period. However, the METH-induced conditioned locomotion was unaffected by the pretreatment with 7-NI. The present study supports the role of brain NO in the development of sensitization to both psychostimulants, cocaine and METH. However, it appears that the inability of 7-NI to completely abolish the sensitized responses induced after METH administration is the result of the resistible conditioned locomotion caused by METH, but not by cocaine.
有证据表明,在与精神运动刺激相关的脑结构中,多巴胺、谷氨酸和一氧化氮(NO)之间存在多种相互作用。本研究旨在探讨神经元型一氧化氮合酶(NOS)同工型的相对选择性抑制剂7-硝基吲唑(7-NI)对可卡因和甲基苯丙胺(METH)运动刺激作用致敏性发展的影响。雄性瑞士韦伯斯特小鼠每天接受15mg/kg可卡因,连续5天,在停药10天后,对挑战剂量的可卡因(15mg/kg)产生明显的运动致敏性,或对挑战剂量的METH(0.5mg/kg)注射产生交叉致敏性。这种处理还产生了情境依赖性致敏,这可通过对挑战剂量生理盐水注射的致敏反应来证明。在给予可卡因(5天)前30分钟用7-NI(25mg/kg)预处理,完全阻断了对可卡因的致敏诱导、对METH的交叉致敏以及可卡因诱导的条件性运动。单独给予7-NI,无论是急性给药还是连续5天给药,对动物的运动活性均无显著影响。用METH(1.0mg/kg)处理5天的动物对挑战剂量的METH(0.5mg/kg)产生明显的致敏性、对挑战剂量的可卡因(15mg/kg)产生交叉致敏性以及情境依赖性运动。在停药10天后,用7-NI(25mg/kg)预处理减弱了对METH的致敏反应和对可卡因的交叉致敏反应。然而,METH诱导的条件性运动不受7-NI预处理的影响。本研究支持脑NO在对精神兴奋剂可卡因和METH的致敏性发展中的作用。然而,7-NI不能完全消除METH给药后诱导的致敏反应,这似乎是METH而非可卡因引起的抵抗性条件性运动的结果。