Talarek Sylwia, Listos Joanna, Orzelska-Gorka Jolanta, Jakobczuk Malgorzata, Kotlinska Jolanta, Biala Grazyna
Chair and Department of Pharmacology and Pharmacodynamics, Medical University of Lublin, Chodzki 4A, 20-093, Lublin, Poland.
Neurotox Res. 2017 Feb;31(2):309-316. doi: 10.1007/s12640-016-9688-3. Epub 2016 Dec 12.
The goal of the study was to investigate the effects of drugs modifying L-arginine:NO:cGMP pathway on the development of tolerance to flunitrazepam (FNZ)-induced motor impairment in mice. FNZ-induced motor incoordination was assessed on the 1st and 8th days of experiment, using the rotarod and chimney tests. It was found that (a) both a non-selective nitric oxide synthase (NOS) inhibitor: N -nitro-L-arginine methyl ester (L-NAME) and an unselective neuronal NOS inhibitor: 7-nitroindazole (7-NI) inhibited the development of tolerance to the motor-impairing effects of FNZ in the rotarod and the chimney tests and (b) both a NO precursor: L-arginine and a selective inhibitor of phosphodiesterase 5 (PDE5): sildenafil did not affect the development of tolerance to FNZ-induced motor impairment in mice. Those findings provided behavioural evidence that NO could contribute an important role in the development of tolerance to FNZ in mice.
本研究的目的是探讨改变L-精氨酸:一氧化氮:环磷酸鸟苷(cGMP)途径的药物对小鼠氟硝西泮(FNZ)诱导的运动功能损害耐受性发展的影响。在实验的第1天和第8天,使用转棒试验和烟囱试验评估FNZ诱导的运动不协调。结果发现:(a)非选择性一氧化氮合酶(NOS)抑制剂N-硝基-L-精氨酸甲酯(L-NAME)和非选择性神经元NOS抑制剂7-硝基吲唑(7-NI)在转棒试验和烟囱试验中均抑制了对FNZ运动损害作用耐受性的发展;(b)一氧化氮前体L-精氨酸和磷酸二酯酶5(PDE5)选择性抑制剂西地那非均不影响小鼠对FNZ诱导的运动损害耐受性的发展。这些发现提供了行为学证据,表明一氧化氮在小鼠对FNZ耐受性的发展中可能起重要作用。