Uhlírová L, Sustková-Fiserová M, Krsiak M
Department of Pharmacology, Charles University, 3rd Faculty of Medicine, Ruská 87, 100 34 Prague 10, Czech Republic.
Psychopharmacology (Berl). 2004 Jan;171(3):259-69. doi: 10.1007/s00213-003-1583-y. Epub 2003 Sep 5.
Flumazenil, a competitive antagonist of benzodiazepine receptors (BZRs), has been used as a probe to detect effects of putative endogenous ligands for BZRs in anxiety. Flumazenil is renowned for its highly inconsistent behavioral effects.
To ascertain effects of flumazenil in the social conflict test in mice, which provides complex measures for prediction of anxiolytic and anxiogenic activity of drugs in behaviorally different groups of animals.
Singly housed male mice treated with flumazenil (5, 20 or 80 mg/kg i.p.) or vehicle were paired with untreated non-aggressive group-housed male mice in a novel cage. Behavior was analyzed from video tapes of the social interactions in three populations of mice: timid (n=21), aggressive (n=11), and sociable (n=7). Levels of gamma-aminobutyric acid (GABA) were measured in vivo in the prefrontal cortex.
Flumazenil reduced timid (defensive-escape) and increased locomotor activities in timid mice. The drug reduced aggressive and increased sociable (social investigation) activities in aggressive mice. These behavioral changes were produced at the lowest dose of flumazenil tested (5 mg/kg) and were not increased further by higher doses of the drug (20 mg/kg or 80 mg/kg). A tendency to increased timidity was found after flumazenil in sociable mice. Concentrations of GABA were markedly higher in the prefrontal cortex of sociable mice than in timid or aggressive mice.
Flumazenil produced moderate anxiolytic-like behavioural changes and a slight anxiogenic-like effect. The present data might be reflecting antagonism of corresponding endogenous BZR ligands. However, these putative ligands seem to exert only modest modulatory influence.
氟马西尼是苯二氮䓬受体(BZRs)的竞争性拮抗剂,已被用作一种探针,以检测假定的内源性配体对焦虑中BZRs的影响。氟马西尼因其行为效应高度不一致而闻名。
确定氟马西尼在小鼠社会冲突试验中的作用,该试验为预测行为不同的动物群体中药物的抗焦虑和致焦虑活性提供了复杂的指标。
将腹腔注射氟马西尼(5、20或80mg/kg)或溶剂的单独饲养的雄性小鼠与未处理的非攻击性群居雄性小鼠配对,置于一个新笼子中。从三组小鼠(胆小的,n=21;好斗的,n=11;友善的,n=7)社会互动的录像带中分析行为。在体测量前额叶皮质中γ-氨基丁酸(GABA)的水平。
氟马西尼减少了胆小小鼠的胆小行为(防御性逃避)并增加了其运动活动。该药物减少了好斗小鼠的攻击行为并增加了其友善行为(社交探究)。这些行为变化在测试的最低剂量氟马西尼(5mg/kg)时就已产生,更高剂量(20mg/kg或80mg/kg)并未使其进一步增强。在友善小鼠中,氟马西尼给药后发现有胆小倾向增加。友善小鼠前额叶皮质中GABA的浓度明显高于胆小或好斗小鼠。
氟马西尼产生了适度的抗焦虑样行为变化和轻微的致焦虑样效应。目前的数据可能反映了相应内源性BZR配体的拮抗作用。然而,这些假定的配体似乎仅发挥适度的调节影响。