Kayir Hakan, Ceyhan Mert, Yavuz Oğuzhan, Uzbay I Tayfun
Department of Medical Pharmacology, Psychopharmacology Research Unit, Gulhane Military Medical Academy, Etlik 06018, Ankara, Turkey.
Synapse. 2007 Oct;61(10):869-74. doi: 10.1002/syn.20440.
The present study was designed to investigate the effects of Nomega-nitro-L-arginine methyl ester (L-NAME), a nitric oxide (NO) synthase inhibitory agent, on bromocriptine-induced locomotor sensitization in mice. Adult male Swiss-Webster mice (26-32 g) were the subjects. Saline or L-NAME (15-60 mg/kg) was injected to mice intraperitoneally 30 min before bromocriptine (5 mg/kg), and locomotor activity was recorded for 240 min in an open field activity monitoring system. This procedure lasted for 2 weeks, once in 2 days from Monday to Friday, six sessions in total. After a 2-day drug-free period, a challenge injection of bromocriptine (5 mg/kg) or vehicle was administered by all groups of mice. Other groups of mice treated with bromocriptine according to the aforementioned procedure except L-NAME pretreatments were challenged with saline or L-NAME (15-60 mg/kg) plus bromocriptine (5 mg/kg) after a 2-day drug-free period. Bromocriptine produced a significant locomotor sensitization. L-NAME (15-60 mg/kg) did not have any significant effect on the development and expression of bromocriptine-induced locomotor sensitization in mice. Meanwhile, the data also imply that NO-related mechanisms may not be responsible for bromocriptine-induced locomotor sensitization in mice.
本研究旨在探讨一氧化氮(NO)合酶抑制剂Nω-硝基-L-精氨酸甲酯(L-NAME)对溴隐亭诱导的小鼠运动致敏的影响。成年雄性瑞士-韦伯斯特小鼠(26 - 32克)作为实验对象。在注射溴隐亭(5毫克/千克)前30分钟,给小鼠腹腔注射生理盐水或L-NAME(15 - 60毫克/千克),并在旷场活动监测系统中记录240分钟的运动活性。此过程持续2周,从周一至周五每2天进行一次,共6次。在2天的无药期后,所有小鼠组均注射一次溴隐亭(5毫克/千克)或溶剂。除了L-NAME预处理外,其他按照上述程序用溴隐亭处理的小鼠组在2天无药期后,用生理盐水或L-NAME(15 - 60毫克/千克)加溴隐亭(5毫克/千克)进行激发注射。溴隐亭产生了显著的运动致敏。L-NAME(15 - 60毫克/千克)对溴隐亭诱导的小鼠运动致敏的发展和表达没有任何显著影响。同时,数据还表明,与NO相关的机制可能与溴隐亭诱导的小鼠运动致敏无关。