Marras R A, Martins A P, Del Bel E A, Guimarães F S
Department of Pharmacology, FMRP, Ribeirão Preto, SP, Brazil.
Neuroreport. 1995 Dec 29;7(1):158-60.
The objective of this study was to investigate possible motor effects of NG-nitro-L-arginine (L-NOARG), an inhibitor of nitric oxide synthase. Acute administration of L-NOARG (5-80 mg kg-1, i.p.) induced catalepsy in a dose-dependent manner in male albino-Swiss mice. The drug had an additive effect with haloperidol (0.125-0.5 mg kg-1, i.p.). The acute effect of L-NOARG (40 mg kg-1, i.p.) was attenuated by previous treatment with L-arginine (300 mg kg-1, i.p.). Sub-chronic treatment with L-NOARG (40 mg kg-1, i.p., twice a day for 4 days) was also able to attenuate the cataleptic effect of acute drug administration (40 mg kg-1, i.p.). These results show that acute systemic injections of L-NOARG induce significant motor effects.
本研究的目的是调查一氧化氮合酶抑制剂NG-硝基-L-精氨酸(L-NOARG)可能的运动效应。急性给予L-NOARG(5-80毫克/千克,腹腔注射)可使雄性白化瑞士小鼠出现剂量依赖性的僵住症。该药物与氟哌啶醇(0.125-0.5毫克/千克,腹腔注射)有相加作用。预先给予L-精氨酸(300毫克/千克,腹腔注射)可减弱L-NOARG(40毫克/千克,腹腔注射)的急性效应。亚慢性给予L-NOARG(40毫克/千克,腹腔注射,每天两次,共4天)也能够减弱急性药物给药(40毫克/千克,腹腔注射)的僵住症效应。这些结果表明,急性全身注射L-NOARG可诱导显著的运动效应。