Podhorna J, Brown R E
Department of Psychology, Dalhousie University, Halifax, Nova Scotia, Canada.
Eur J Pharmacol. 1999 Oct 15;382(3):143-50. doi: 10.1016/s0014-2999(99)00595-6.
The present study investigated the effects of drugs acting on the brain nitric oxide pathway on ultrasonic vocalizations, body temperature and locomotion in 7-8-day-old rat pups. Both a selective neuronal nitric oxide synthase (NOS) inhibitor (7-nitroindazole) and a non-selective NOS inhibitor (nitro-L-arginine-methyl ester, L-NAME) decreased the number of ultrasonic vocalizations in a dose-dependent manner. The non-selective NOS inhibitor, L-NAME, suppressed not only ultrasonic vocalizations but also locomotion. The inactive isomer of the NOS inhibitor, nitro-D-arginine-methyl ester (D-NAME), and the biological precursor of nitric oxide, L-arginine, had no effect on ultrasonic vocalizations or locomotion. These data indicate that drugs suppressing nitric oxide synthesis produced an anxiolytic effect in rat pups. However, only the selective NOS inhibitor, 7-nitroindazole, was 'anxioselective', i.e., reduced ultrasonic vocalizations without causing sedation. Increased synthesis of nitric oxide in the brain had no apparent behavioral effect in this model.
本研究调查了作用于大脑一氧化氮途径的药物对7 - 8日龄大鼠幼崽超声发声、体温和运动的影响。一种选择性神经元一氧化氮合酶(NOS)抑制剂(7 - 硝基吲唑)和一种非选择性NOS抑制剂(硝基 - L - 精氨酸甲酯,L - NAME)均以剂量依赖的方式减少了超声发声的次数。非选择性NOS抑制剂L - NAME不仅抑制了超声发声,还抑制了运动。NOS抑制剂的无活性异构体硝基 - D - 精氨酸甲酯(D - NAME)以及一氧化氮的生物前体L - 精氨酸,对超声发声或运动均无影响。这些数据表明,抑制一氧化氮合成的药物在大鼠幼崽中产生了抗焦虑作用。然而,只有选择性NOS抑制剂7 - 硝基吲唑具有“抗焦虑选择性”,即减少超声发声而不引起镇静作用。在该模型中,大脑中一氧化氮合成增加没有明显的行为效应。